The Arabidopsis transcription factor HY5 controls light-induced gene expression downstream of photoreceptors and plays an important role in the switch of seedling shoots from dark-adapted to light-adapted development. In addition, HY5 has been implicated in plant hormone signaling, accounting for the accelerated root system growth phenotype of hy5 mutants. Mutants in the close HY5 homolog HYH resemble wild-type, despite the largely similar expression patterns and levels of HY5 and HYH, and the functional equivalence of the respective proteins. Moreover, the relative contribution of HYH to the overall activity of the gene pair is increased by an alternative HYH transcript, which encodes a stabilized protein. Consistent with the enhanced root system growth observed in hy5 loss-of-function mutants, constitutively overexpressed alternative HYH inhibits root system growth. Paradoxically, however, in double mutants carrying hy5 and hyh null alleles, the hy5 root growth phenotype is suppressed rather than enhanced. Even more surprisingly, compared to wild-type, root system growth is diminished in hy5 hyh double mutants. In addition, the double mutants display novel shoot phenotypes that are absent from either single mutant. These include cotyledon fusions and defective vasculature, which are typical for mutants in genes involved in the transcriptional response to the plant hormone auxin. Indeed, many auxin-responsive and auxin signaling genes are misexpressed in hy5 mutants, and at a higher number and magnitude in hy5 hyh mutants. Therefore, auxin-induced transcription is constitutively activated at different levels in the two mutant backgrounds. Our data support the hypothesis that the opposite root system phenotypes of hy5 single and hy5 hyh double mutants represent the morphological response to a quantitative gradient in the same molecular process, that is gradually increased constitutive auxin signaling. The data also suggest that HY5 and HYH are important negative regulators of auxin signaling amplitude in embryogenesis and seedling development.
Genetic redundancy is the total or partial compensation of inactivation of one gene by another, usually related gene. In Arabidopsis, HY5 and HYH are highly similar, principally exchangeable genes. However, only inactivation of HY5 results in morphological defects, indicating that HY5 plays a more important role in development than HYH. Nevertheless, if inactive versions of such partially redundant genes are combined in a double mutant, the defects observed in the single mutant often worsen. Paradoxically, however, combined inactivation of HY5 and HYH leads to a defect that is opposite to inactivation of HY5 alone: compared to controls, root system growth is decreased in the double mutant, rather than enhanced as in plants only lacking HY5 activity. Through careful analysis of the double mutant defects and scans of genome-wide gene expression levels, the authors determined that the opposite root system growth of hy5 single and hy5 hyh double mutants is a morphological response to a gradually increased quantitative disturbance in the same molecular process, the physiological response to the plant hormone auxin. This example suggests that inactivation of genes that quantitatively affect the balance of a physiological process in the same manner might manifest in very different morphological changes.
Citation: Sibout R, Sukumar P, Hettiarachchi C, Holm M, Muday GK, Hardtke CS (2006) Opposite Root Growth Phenotypes of hy5 versus hy5 hyh Mutants Correlate with Increased Constitutive Auxin Signaling. PLoS Genet 2(11): e202. https://doi.org/10.1371/journal.pgen.0020202
Editor: John Doebley, University of Wisconsin, United States of America
Received: August 21, 2006; Accepted: October 16, 2006; Published: November 24, 2006
Copyright: © 2006 Sibout et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: This work was funded by the Canton de Vaud (RS, CSH), a grant from the Swedish Research Council (MH), and the Wake Forest University Science Research Fund (GKM). CH was supported by a Carl Trygger Foundation fellowship.
Competing interests: The authors have declared that no competing interests exist.
Abbreviations: altHYH, alternative HYH transcript; CAB, chlorophyll a/b binding protein; CHS, chalcone synthase; COP1, CONSTITUTIVE PHOTOMORPHOGENIC 1; flHYH, full-length HYH; HY5, LONG HYPOCOTYL 5; HYH, HY5 HOMOLOG; qPCR, quantitative real-time RT-PCR; tt4, transparent testa 4
Homologous genes of the same family display genetic redundancy to varying degrees if their expression pattern and their function overlap. In general, loss-of-function mutations of redundantly acting genes are expected to result in no phenotype in the case of full redundancy, or similar phenotypes in the case of partial redundancy. If the mutations in partially redundant genes are combined, an enhancement of the single mutant phenotypes is expected. In this study, we investigated the genetic redundancy between two functionally equivalent Arabidopsis transcription factors. Surprisingly, their combined loss-of-function leads to a phenotype that is opposite to what would be expected from the single mutant phenotypes. These two genes have been originally identified because of their role in light signaling.
Light is arguably the most important stimulus in plant development, since growth and reproductive success ultimately depend on the energy harvested from light by photosynthesis. To sense the intensity, direction, and spectral quality of light, plants have developed sophisticated molecular networks . Plants also possess circadian clocks to measure day length and to adjust their physiology in anticipation of dawn . Within the light-sensing network, a few factors have a central role in the downstream transcriptional response. Their importance is particularly evident in the most extreme light environment transition in the plant life cycle, the transition from dark-adapted (skotomorphogenic) to light-adapted (photomorphogenic) development.
Skotomorphogenic seedlings display closed cotyledons, which protect the shoot meristem, reduced root growth, and strongly enhanced hypocotyl elongation. By this behavior, seedlings concentrate their resources toward pushing the shoot meristem through the soil into the light in nature. Light exposure then triggers photomorphogenesis, which comprises light-induced gene expression, cotyledon expansion, photosynthesis, suppression of hypocotyl elongation, and acceleration of root and shoot growth. Factors involved in the transition from skotomorphogenesis to photomorphogenesis have mainly been identified in Arabidopsis. Among them, the basic leucine zipper (bZIP) transcription factors LONG HYPOCOTYL 5 (HY5) and HY5 HOMOLOG (HYH) play an important role in light-induced gene expression. Loss-of-function hy5 mutants display dark-grown characteristics in the light , most significantly, a loss of the inhibition of hypocotyl elongation. While hy5 mutants display this phenotype in all light conditions, mutants in hyh show a similar but very weak phenotype only in blue light .
A general characteristic of the transition from skotomorphogenesis to photomorphogenesis is the suppression of cell expansion in some organs, for instance, the hypocotyl, increased cell expansion in others, e.g., the cotyledons, and the onset of growth by cell division in the shoot and root meristems. Notably, both cell expansion and division are thought to be under crucial control of plant hormone signals. Thus, it has long been suspected that light signaling must intersect with hormone signaling or biosynthesis pathways to elicit the desired responses. In fact, several plant hormones have been implicated in light signaling, because they influence cell expansion and/or division, or light-regulated gene expression [5–9]. Among them, auxin is of particular interest, because it is known to regulate cell elongation as well as division in a dosage-dependent fashion. Accordingly, several genes that act within the auxin signaling framework have been implicated in light responses [10–14].
HY5 has also been implicated in auxin signaling, partly based on photomorphogenic traits of hy5 mutants [3,15] but mainly because of the hy5 root system phenotypes. The Arabidopsis root system is dominated by a primary root, which is formed during embryogenesis. After germination, this primary root grows, driven by the cell proliferation and elongation taking place in its apical meristem. Once the primary root has reached a certain length several days after germination, the root system extends through the formation of lateral roots, which emerge along the primary root. In hy5 mutants, the emergence of lateral roots occurs earlier than in wild-type, resulting in overall enhanced root system growth [3,15]. Moreover, the gravitropism of hy5 roots is reduced. Both lateral root formation and root gravitropism are known to require an intact auxin signaling pathway.
Here we present a detailed analysis of the genetic redundancy between HY5 and its homolog, HYH, which revealed paradoxically opposite root system phenotypes of hy5 single versus hy5 hyh double mutants. These phenotypes correlate with quantitatively different constitutive auxin signaling in the mutants. Our data suggest that both genes act redundantly as quantitative modulators of auxin signaling and have a much more central role in this process than anticipated from their respective single mutant phenotypes. This role goes far beyond their role in light signaling and impinges on embryogenesis, root development, shoot development, and vascular differentiation.
The Expression Patterns of HY5 and HYH Are Largely Similar
In contrast to the pronounced seedling shoot phenotypes of hy5 null mutants, hyh null mutants display only very weak phenotypes and only so in blue light. These are slightly decreased anthocyanin biosynthesis and slight decreased inhibition of hypocotyl elongation . In darkness and white light, hyh mutants resemble wild-type. The discrepancy between the hy5 and hyh mutant phenotypes could be explained by differential expression patterns of the two genes. To test this hypothesis, we constructed transgenic plants expressing a GFP reporter gene under control of either the HY5 or the HYH promoter. Similar expression patterns for each construct were observed in several independent transgenic lines (Figure 1). In several-day-old light-grown seedlings, HY5 is expressed mainly in the hypocotyl and only very weakly in the cotyledons (Figure 1B and 1F). At this stage, HYH is expressed throughout the seedling as well, but at a clearly higher level than HY5 (Figure 1C and 1G). In dark-grown seedlings, both genes are expressed in the apical region of the hypocotyl and in the cotyledons (Figure 1D and 1E). Both genes are also strongly expressed throughout the proliferation zone of the root meristem (Figure 1H and 1I). In the elongation zone, expression becomes gradually concentrated in the vasculature (Figure 1J and 1K), where both genes are primarily expressed in the mature root (Figure 1L and 1M). Thus, in general, the expression patterns of HY5 and HYH are largely identical.
(A–M) Analysis of transgenic wild-type plants expressing the GFP reporter (green fluorescence) under control of the HY5 (B, D, F, H, J, L) or HYH (C, E, G, I, K, M) promoter. Seedling shape is indicated by a broken line in (A–C) for clarity.
(A) A light-grown wild-type control seedling.
(B and C) Light-grown seedlings at 5 d after germination.
(D and E) Apical part of the hypocotyl of dark-grown seedlings, including cotyledons.
(F and G) Close-up of the hypocotyl of light-grown seedlings.
(H and I) Primary root tip.
(J and K) Elongation zone of the primary root meristem.
(L and M) Mature part of the primary root. Images (A–D) have been acquired by fluorescence microscopy, (E–J) by confocal microscopy.
(N) qPCR quantification of HY5 and HYH transcripts in dark-grown seedlings (t = 0) shifted into the light (intensity 5 μE), assayed at given time points. Transcript quantity is expressed in relation to the control gene EF1.
(O) Abundance of HY5 and HYH transcripts in shoots or roots of 6-d-old seedlings measured by qPCR. Seedlings were grown in constant light at an intensity of 100 μE. Transcript quantity is expressed in relation to the control gene EF1.
(P) Alignment of conceptually translated ORFs of HY5 and HYH cDNAs. The COP1 interaction domain is underlined. altHYH indicates protein derived from alternatively spliced HYH transcript; flHYH, protein derived from full-length HYH transcript.
(Q) Western analysis of dark-induced degradation of endogenous HYH proteins. Seven-day-old light-grown seedlings were shifted into darkness and samples were removed at the indicated time points. The two HYH isoforms detected by anti-HYH antibody are indicated by arrowheads. Cross-hybridizing bands serve as loading control and can be identified by comparison with the extract from hyh null mutants. Expected protein sizes are 15.2 and 16.9 kDa, and observed sizes are 18 and 25 kDa for altHYH and flHYH, respectively. The discrepancy is likely due to the highly charge of the proteins .
(R) Western analysis of dark-induced degradation of transgenic HYH proteins. Six-day-old light-grown seedlings expressing either flHYH or altHYH under control of the 35S promoter were kept in the dark for 24 h and compared to controls that were kept in the light. The two HYH isoforms detected by anti-HYH antibody are indicated by arrowheads. Endogenous HYH proteins (see N) are not detected because the transgenes were expressed in a hy5 hyh background. Error bars represent standard error of the mean.
Expression Dynamics of HY5 and HYH
Differences in expression level rather than pattern could provide an alternative explanation for the different importance of the two genes. For instance, the absence of phenotypes in hyh mutants could mean that HYH is expressed at much lower levels than HY5. However, the GFP fluorescence in the HYH reporter lines rather appeared to be consistently higher than in the HY5 lines in light-grown conditions, where the hy5 phenotypes manifest. To confirm the quantitative difference proposed by the reporter genes, we determined endogenous HY5 and HYH transcript abundance by quantitative real-time RT-PCR (qPCR) in seedlings. Because we detected a truncated alternative HYH transcript (altHYH) in pilot RT-PCR experiments, the qPCR experiments were designed to differentiate between altHYH and full-length HYH (flHYH).
In the dark, HYH transcripts are present at very low levels, while HY5 is roughly ten times more abundant (Figure 1N). Upon light stimulus, HY5 expression is strongly induced 10- to 12-fold within 1 h, before dropping back to approximately twice its dark level within 6 h (Figure 1N). The expression of both HYH transcripts is also highly light inducible (approximately 50- to 100-fold; Figure 1N) but at a slower pace. Upon light stimulus, HYH levels increase steadily, eventually reaching levels comparable to the later steady state levels of HY5. However, the two HYH transcripts in combination are about twice as abundant as HY5 in light-grown seedlings (Figure 1N and 1O). Examination of dissected light-grown shoots and roots reveals that the excess of HYH as compared to HY5 transcript is restricted to the shoot (Figure 1O), with a ratio of HYH to HY5 transcripts of roughly 6-fold. By contrast, in roots the abundance of HY5 transcript is approximately equal to the abundance of the combined HYH transcripts. Thus, in the conditions where hy5 phenotypes are evident, HYH levels are similar to or higher than HY5 levels.
altHYH Is Less Susceptible to Proteasome-Mediated Degradation
Another explanation for the differential activity of the two genes could be differential activity of the respective proteins. In this context, altHYH is of particular interest, because in the altHYH transcript the coding region for the COP1-interaction domain  is spliced out (Figure 1P). CONSTITUTIVE PHOTOMORPHOGENIC 1 (COP1) is a ubiquitin ligase, which targets both HY5 and HYH for proteasome-mediated degradation in the dark [4,17,18]. This process requires the presence of the COP1-interaction domain . Thus, altHYH should not be susceptible to COP1-mediated proteasomal degradation. Anti-HYH antibodies detect a protein, previously interpreted to be an flHYH degradation product , which unlike flHYH is not degraded when seedlings are shifted from light to darkness (Figure 1Q). Just like flHYH, this band is missing in hyh mutants. To confirm that it represents altHYH, we constructed transgenic plants constitutively overexpressing altHYH or flHYH ORFs under control of the cauliflower mosaic virus 35S promoter. The transgenic proteins are detected at similar molecular weight as the endogenous ones. Transgenic altHYH is also not susceptible to degradation in darkness (Figure 1R), suggesting that the corresponding endogenous band is indeed altHYH.
We also introduced the transgenes into a hy5 background and assayed their capability to rescue hy5 phenotypes. Consistent with previous reports [4,19], 35S:flHYH fully compensates the lack of HY5 in photomorphogenesis, similar to a 35S:HY5 control construct. The 35S:flHYH transgene also normalizes the hy5 root system phenotypes, indicating that HYH can in principle replace HY5 in all aspects of seedling development. 35S:altHYH also complements hy5 phenotypes, but even beyond wild-type levels: hypocotyl elongation is more strongly suppressed than in wild-type (Figure 2A), as is lateral root emergence (Figure 2B), while root greening is exaggerated (Figure 2C). Moreover, hy5 seedlings complemented by altHYH also display slightly but significantly reduced primary root growth (Figure 2D). Thus, the results indicate that HY5 and HYH proteins can act functionally equivalent in both shoot and root development. Because the transgenic plants were assayed in constant light conditions, it also appears that altHYH is more active than flHYH.
Analyses of independent transgenic lines constitutively overexpressing altHYH or flHYH under control of the 35S promoter in a hy5 background.
(A) Hypocotyl length.
(B) Lateral root phenotypes of representative plantlets.
(C) Root greening phenotypes of representative plants.
(D) Primary root length. Plant age: (A and D) = 8 dag (days after germination); (B) = 13 dag; (C) = 30 dag. Error bars represent standard error of the mean.
Root System Growth Is Decreased in hy5 hyh Mutants
In the two blue light–specific described traits of hyh, anthocyanin biosynthesis and hypocotyl elongation, hy5 and hyh behave additively: the relative change conferred by one mutation is proportionally increased by the relative impact of the other mutation . Unlike hy5 mutants, hyh mutants do not display any root system phenotypes. Nevertheless, in hy5 hyh double mutants, the agravitropism observed in hy5 roots is considerably enhanced (Figure 3A). Moreover, the root system growth phenotype of the double mutants represents a reversal of the hy5 phenotype, because lateral root emergence is delayed rather than enhanced (Figure 3B). Also, the total number of lateral roots formed in the double mutants is reduced (Figure 3C). However, lateral root density is largely similar to wild-type, at least early on (Figure 3D). This is because primary root growth is decreased in the double mutant (Figure 3E). The mature root cell size in the double mutants is similar to the single mutants and wild-type (data not shown), but root meristem size is considerably decreased (Figure 3F). Thus, hy5 hyh mutants display reduced root growth because of reduced cell proliferation in the meristem. Delayed formation of lateral organs appears to be a general feature of hy5 hyh double mutants, since adventitious root formation on hypocotyls from dark-grown seedlings shifted into light is also delayed (Figure 3G). Finally, the hyh mutation not only suppresses the increased lateral root density in hy5 (Figure 3D) but also suppresses the accelerated growth rate of hy5 lateral roots (Figure 3H). Thus, in summary, root system growth is enhanced in hy5 mutants, not affected in hyh mutants, but decreased in hy5 hyh double mutants.
Phenotypic analyses of wild-type, hy5, hyh, and hy5 hyh seedlings.
(A) Gravitropic response of the root tip (curvature). Time points refer to time after change of the gravity vector by 90 degrees.
(B) Representative seedlings at 8 dag.
(C) Progression of lateral root emergence.
(D) Progression of primary root growth of the seedlings in (C).
(E) Lateral root density of the seedlings in (C) and (D).
(F) Progression of adventitious root formation from the hypocotyl of 5-d-old dark-grown seedlings after shift into the light for the indicated number of days.
(G) Lateral root growth rate in the different genotypes, recorded between 8 and 10 dag.
(H) Quantification of primary root meristem size. Error bars represent standard error of the mean.
Novel Shoot Phenotypes Occur in hy5 hyh Mutants
In hy5 shoots, we observed a previously unnoticed increase in cotyledon size (Figure 4). Although cotyledon size is not affected in hyh, it is synergistically enhanced in the double mutant (Figure 4A). The double mutant cotyledons also display a novel phenotype that is not found in either single mutant, that is an altered arrangement of the vasculature. Wild-type cotyledon vasculature has a stereotypic pattern, consisting of a midvein and two connected loops on each side of it (Figure 4A). In hy5, occasionally three loops or only one loop can be observed. In hy5 hyh double mutants, however, the stereotypic arrangement is always broken and most loops are not closed. Moreover, in a considerable proportion (approximately 15%) of double mutant seedlings, the cotyledons are fused, a phenotype never seen in the wild-type or single mutant lines. The degree of fusion is variable and can range from improper separation of cotyledons at their base (Figure 4C) up to total fusion into one big cotyledon (Figure 4D). The vasculature in fused cotyledons is randomly arranged, with incomplete loops and ramifications. In addition, milder phenotypic classes can be observed, such as altered cotyledon arrangement that results in altered phyllotaxis of early leaves.
Phenotypic analyses of wt, hy5, hyh, and hy5 hyh seedlings.
(A) Darkfield microscopy images of cotyledons cleared for visualization of the vasculature. The values for each genotype correspond to the average expanded cotyledon size 7 dag in cm2. The respective standard errors of the mean are 0.012, 0.011, 0.019, and 0.023 cm2.
(B) Wild-type cotyledons, before and after clearing.
(C and D) As in (B), for representative fused cotyledons of hy5 hyh seedlings. Note the true leaf opposing the fused cotyledon in (D).
(E) Representative shoots of 12-d-old light-grown seedlings.
(F) Representative first leaves.
(G) Darkfield microscopy images of first leaves, cleared for visualization of the vasculature.
The alterations in the shoot of hy5 hyh seedlings are accompanied by a delayed leaf development (Figure 4E). In particular, the emergence of the first true leaves is significantly delayed, and they display a strong hyponasty (Figure 4F). They also display a strong vascular phenotype, which is again absent from the single mutants. Similar to the cotyledons, the vein pattern is altered, and in addition, the number of strands and ramifications is reduced (Figure 4G). Moreover, the primary veins in the blade run toward the base of the leave instead of away from it. Interestingly, this phenotype is strong in the first four leaves and less penetrant thereafter.
Transcriptome Alterations in hy5 hyh Are More Severe than in hy5, but Show the Same Trend
The novel phenotypes observed in hy5 hyh double mutants, i.e., reduced root system growth, fused cotyledons, and defective vasculature pattern, are reminiscent of the defects typically observed in many auxin signaling mutants. To determine whether auxin signaling is affected in hy5 hyh mutants, we investigated the transcriptome of the double mutants by microarray analyses.
Microarray analyses have been performed previously on hy5 and hy5 hyh mutants [4,15]. However, in these experiments, several-day-old, light-grown seedlings were used. At this stage, the different genotypes display significant morphological differences, which could give rise to expression differences of a secondary nature. To minimize such background and get a grasp on genes primarily affected by HY5 and HYH loss of function, we applied a different strategy. We took into account the finding that both HY5 and HYH protein are very low abundant in dark-grown seedlings [4,17], especially if they have never been exposed to light. Further, there are no morphological differences between dark-grown mutant seedlings and wild-type, except for the occasional cotyledon fusions in the double mutants. Upon exposure to light, HY5 and HYH transcription is induced (see above), and HY5 and flHYH proteins are stabilized within 5 h [4,17], reaching levels comparable to those seen in seedlings grown in constant light. Thus, after 5 h, HY5 and HYH should be fully active. Therefore, for microarray analyses we germinated seedlings in the dark for 3 d and then transferred them into the light. Seedlings were then harvested after 6 h of light exposure and total RNA was isolated and hybridized to Affymetrix ATH1 (http://www.affymetrix.com) microarrays to determine the transcriptome profile for the different genotypes.
To extract meaningful expression differences from our data, we then reasoned that wild-type and hyh seedlings do not display morphological differences in the test conditions. Thus, genes that are only different between hyh and wild-type, not between the double mutant and hyh, should not be responsible for the strong phenotypes observed in the double mutant. Rather, only genes that are consistently affected between the double mutant and both wild-type and hyh should be of interest (Figure 5). When applying these criteria, the expression levels of 627 genes (approximately 2.7% of all genes on the array) differ significantly (p < 0.05), applying a threshold of 2-fold (Table S1 and Figure 5A). Among them, 396 are underexpressed in hy5 hyh and 231 are overexpressed. Consistent with the milder phenotype of hy5 single mutants compared to the double, only a subset of 263 (approximately 42%) of those genes is affected in hy5 compared to wild-type (Figure 5A). One hundred fifty-one genes are underexpressed and 112 are overexpressed, and the direction of misregulation is generally similar to what is observed for those genes in the double mutant.
(A) Total number of genes consistently underexpressed or overexpressed in hy5 hyh seedlings when compared to wild-type. The inlaid circles represent the subset of genes that are already affected in the hy5 mutant, with underexpression or overexpression compared to wild-type.
(B) Subset of the genes presented in (A) that are repressed by auxin application in wild-type. The inlaid circles represent the auxin response of this set of genes in hy5 or hy5 hyh.
(C) Subset of the genes presented in (A) that are induced by auxin application in wild-type. The inlaid circles represent the auxin response of this set of genes in hy5 or hy5 hyh. Red indicates underexpressed in (A) and repressed in (B) and (C). Green indicates overexpressed in (A) and induced in (B) and (C). Blue in (B) and (C) indicates genes that are not auxin responsive any longer in the mutant genotypes.
(D–G) Confirmation of the expression levels of the indicated representative genes in replicate samples used in (A) by qPCR quantification. Transcript quantity is expressed relative to the control gene EF1.
We searched our gene list for functionally defined genes that could explain the hy5 and hy5 hyh phenotypes (Table 1). As expected, we found a number of light-regulated genes that have partly been reported to be under HY5 control, e.g., chalcone synthase (CHS) genes or chlorophyll a/b binding protein (CAB) genes and other components of the photosynthetic apparatus (16 genes in total) [4,15,20,21]. Other overrepresented, annotated gene classes that are misregulated in the double mutant include many transcription factors (57 genes) as well as ubiquitin ligase components (24 genes). Among the genes that stand out are CIRCADIAN CLOCK ASSOCIATED 1 (CCA1) , a circadian clock regulator previously suspected to be under HY5 control , and CUP-SHAPED COTYLEDON 1 (CUC1), a gene involved in the organization of the apical embryo . We confirmed the expression level trends of these particular genes in independent biological samples by qPCR experiments (Figure 5D and 5E). CUC1 expression is hardly altered in hy5, but strongly so in the double mutant, consistent with the appearance of cotyledon fusions in the latter. Finally, another notable group of genes are genes that have been described to be involved in auxin-mediated transcriptional response (15 genes). We also confirmed the expression level trends of two genes from this group, ARGOS and INDOLE ACETIC ACID (IAA) 19, independently by qPCR (Figure 5F and 5G). No alterations were detected in the expression of genes that are implicated in auxin transport. Moreover, genes described to play a role in other hormone signaling pathways are conspicuously absent from our set, with the exception of four genes involved in gibberellic acid metabolism and one gene involved in ethylene biosynthesis (Table 1).
List of Selected Genes Consistently Misregulated in hy5 hyh Double Mutants, Ordered According to Functional Classification
In summary, as a general trend, the genes that are misregulated in hy5 represent a subset of the genes misregulated in the double mutant. Moreover, the magnitude of misregulation is generally higher in the double mutant than in hy5.
Constitutive Auxin-Induced Gene Expression in hy5 and hy5 hyh Mutants
Because of the preponderance of auxin-related genes among the hormone-related ones, we investigated auxin-induced gene expression. Samples were grown in darkness for 3 d, exposed to light for 5 h, and then treated with externally applied auxin for 1 h. In the analysis of the respective microarrays, we concentrated on the set of 627 genes consistently affected in the double mutant. Of these, 246 (approximately 39%) were auxin-responsive in wild-type (threshold 2-fold, p < 0.05), with 129 genes being repressed and 117 genes being induced. A large proportion of these genes do not respond properly to auxin in hy5 (166 genes, or approximately 66%) and the double mutant (199 genes, or approximately 82%) (Figure 5B and 5C and Table S1).
Of the 246 auxin-responsive genes of the wild-type, 112 do not respond to auxin treatment in hy5 hyh (i.e., approximately 46%; Figure 5B and 5C and Table S2). Most of those genes are highly misexpressed in untreated seedlings. Among the 66 genes that are induced by auxin in the wild-type, 62 are overexpressed in the double mutant, and of the 46 auxin-repressed genes, 39 are highly underexpressed. Thus, the data indicate that many auxin-responsive genes are constitutively expressed at auxin-induced or -repressed levels in hy5 hyh mutants.
Of the 112 genes that do not respond to auxin in the double mutant any longer, 58 are equally affected in hy5 single mutants. The other 54 genes still react to auxin. In a small number of cases, opposite regulation in wild-type and hy5 can be observed; however, as a general trend, with respect to auxin-regulated transcription, hy5 mutants represent a mild version of hy5 hyh double mutants. This gradual increase in disturbance of auxin signaling is particularly evident in the expression of a number of well-characterized auxin-responsive genes. Some of these genes are involved in auxin signaling and have been described in the context of hypocotyl elongation and/or photomorphogenesis. For instance, SHY1/IAA6  is mildly overexpressed in hy5 (approximately 2-fold), more affected in the double mutant (approximately 3-fold), still auxin inducible in hy5, but no longer auxin inducible in the double mutant (Table 1). The same is true for IAA19/MSG2 . In some cases, the gene is not affected in hy5 but is in the double mutant, as seen for IAA2. A similar pattern can be observed for numerous other genes (e.g., Table 1). Moreover, in the set of 246 genes that are auxin responsive in the wild-type, many genes can be found whose auxin responsiveness is greatly diminished in hy5 and/or hy5 hyh (Tables 1 and S1). Prominent examples include IAA1  (not affected in hy5, approximately 2.5-fold overexpressed in hy5 hyh, auxin responsiveness reduced to approximately 2.8-fold in hy5 hyh from approximately 9-fold in the wild-type) and ARGOS , a gene implicated in auxin-dependent lateral organ formation (not affected in hy5, approximately 4-fold overexpressed in hy5 hyh, auxin responsiveness reduced to approximately 5 and approximately 2-fold in hy5 and hy5 hyh, respectively, down from approximately 7-fold in the wild-type). Similar patterns can be found for many genes annotated as auxin responsive, for instance, SAUR-AC1 (approximately 2-fold overexpressed in hy5, approximately 3-fold in hy5 hyh, auxin responsiveness decreased from approximately 10-fold in wild-type to approximately 6-fold and approximately 2-fold in hy5 and hy5 hyh, respectively). Finally, for a number of genes, inverse patterns can be observed (Tables 1 and S1); that is, they are repressed by auxin in the wild-type, but this repression is lost in hy5 hyh or hy5, because the respective genes are already underexpressed in those mutants.
In summary, the expression of many auxin-responsive genes is disturbed in hy5 mutants and increasingly so in hy5 hyh double mutants. Comparison with the transcriptome data from untreated seedlings reveals that this lack of auxin response is generally reflecting a constitutive level of auxin-induced transcription in the mutants. This constitutive level is more severe in hy5 hyh mutants than in hy5 mutants
Polar Auxin Transport Is Altered in hy5 and hy5 hyh Roots
Our microarray and phenotypic data implicate HY5 and HYH primarily in auxin response at the transcription level. However, it is possible that the phenotypes might at least in part be due to altered auxin transport. For instance, root gravitropism requires correct auxin transport in the root tip . Indeed, consistent with their agravitropism, basipetal auxin transport is reduced in hy5 root tips (Figure 6A). In hyh, basipetal transport is normal, however, and the influence of hyh on this trait in the double mutant, if any, is marginal. Because flavonoids have been identified as regulators of basipetal auxin transport in the root  and because the expression of rate-limiting enzymes in flavonoid biosynthesis, notably CHS, is largely HY5 dependent [15,20,21], we investigated whether hy5 root agravitropism is a secondary consequence of decreased flavonoid biosynthesis. To test this hypothesis, we fed hy5 seedlings with naringenin, thus bypassing the requirement for CHS expression. A similar treatment rescues the flavonoid content and agravitropism of transparent testa 4 (tt4), a null mutant in the principal CHS gene . Sufficient levels of naringenin indeed also restore flavonoid content in the hy5 mutant (Figure 6B); however, agravitropism (Figure 6C) or other hy5 root phenotypes are not rescued.
Physiological analyses of wt, hy5, hyh, and hy5 hyh seedlings.
(A) Relative basipetal auxin transport in the root tip.
(B) Naringenin feeding restores flavonoid content in hy5. Fluorescent imaging of flavonoids in the primary root tip of hy5 and the control genotypes wild-type (Col) and tt4. Naringenin concentrations are indicated in the lower right corner in μM. Values in the upper left corner represent quantification of flavonoid fluorescence relative (%) to wild-type.
(C) Gravitropic response of the root tip (curvature) in wild-type, hy5, and hy5 treated with 25 μM naringenin. Time points refer to time after change of the gravity vector by 90 degrees.
(D) Relative acropetal auxin transport in the root. Error bars represent standard error of the mean.
Opposite to basipetal transport, acropetal auxin transport in hy5 roots is enhanced rather than reduced (Figure 6D). This is also the case in hyh and in double mutant roots; however, no enhancement of this trait is observed in the latter. Thus, both basipetal and acropetal auxin transport are altered in hy5 and hy5 hyh roots.
The Phenotypes of hy5, hyh, and hy5 hyh Mutants: A Paradoxical Situation
Our analysis of the developmental roles of HY5 and HYH revealed two paradoxes. First, hy5 null mutants have dramatic seedling phenotypes, while no morphological phenotype is apparent in hyh null mutants, except slightly defective inhibition of hypocotyl elongation specifically in blue light . In light of our expression analyses, this is surprising. Both genes are expressed in nearly identical patterns, and in light-grown seedlings HYH is more abundant than HY5, although it nevertheless is apparently the dispensable one of the two genes. Finally, the HY5 and HYH proteins are functionally equivalent, because ectopic overexpression of either gene rescues hy5 phenotypes equally well. Importantly, neither gene is required for the expression of the other (R. Sibout, unpublished data). However, it has been described that HYH protein steady state levels are decreased in hy5 . This reduction might be functionally more significant than initially suspected, because of the increased stability of the altHYH protein, which is likely due to the lack of the COP1 interaction domain. Thus, conceptually, hy5 could be considered a weak hy5 hyh double mutant.
The biological significance of the alternative HYH transcript remains to be determined. Although altHYH is expressed at relatively low levels in darkness when compared to HY5, due to the increased stability of altHYH protein, the difference in protein activity is likely less dramatic. Thus, altHYH could have an important role in kick-starting gene expression upon light stimulus and in sustaining light-regulated gene expression once the initial burst of light-induced HY5 transcription is dropping to steady state levels. It is also conceivable that altHYH could play a role in the anticipation of dawn. Although our experiments do not differentiate between diurnal and circadian regulation of HYH, a direct link to the circadian clock is suggested by our finding that its central component CCA1 appears to be under HY5/HYH control.
The second paradox is the discrepancy between the hy5 and double mutant root phenotypes. While lateral root emergence and growth is enhanced in hy5 mutants, this phenotype is suppressed in the double mutants. Moreover, overall root system growth is even diminished in hy5 hyh. This situation correlates with a gradual increase in constitutive auxin signaling in the hy5 hyh versus the hy5 mutant background, as indicated by transcriptome analyses and by the occurrence of novel, auxin-related phenotypes in hy5 hyh double mutant shoots.
A General Role of HY5 and HYH in Auxin Signaling
Initially, HY5 had been suspected to play a role in auxin signaling because of the branching phenotype and agravitropism of hy5 roots . The double mutant, however, implicates HY5 and HYH in auxin signaling in a much wider sense, because the observed novel phenotypes are hallmarks of strongly impaired auxin signaling. The appearance of fused cotyledons in hy5 hyh is an especially specific indicator. Because the cotyledons are formed in the embryo, this phenotype reveals a role for HY5 and HYH in embryogenesis. Cotyledon fusions are observed in a number of auxin signaling embryogenesis mutants, e.g., bodenlos (bdl/iaa12)  or monopteros (mp) . Interestingly, this phenotype is usually not fully penetrant and represents the extreme of a phenotypic range. The hy5 hyh double mutant is similar in this respect: fused cotyledons are only observed in approximately 15% of seedlings. However, the cotyledons of all hy5 hyh seedlings have an altered vasculature, which is also a characteristic of mutants altered in auxin signaling or transport, e.g., mp. The correct separation of cotyledons in embryogenesis requires the three partially redundant CUC genes [24,31]. Among them, CUC2 acts downstream of MP and the auxin transport regulator PIN-FORMED 1 (PIN1) . By contrast, MP and PIN1 do not control embryonic expression of CUC1. Our microarray experiments indicate that the expression level of this gene is strongly altered in hy5 hyh double mutants. Therefore, HY5/HYH control of CUC1 might act as a parallel input to provide maximal CUC activity in embryogenesis. In summary, the strong auxin-related phenotypes of hy5 hyh double mutants, combined with the results from our microarray analyses, suggest that HY5 and HYH have a general role in auxin signaling, from embryogenesis on throughout seedling development.
A Complementary Strategy for Transcriptome Analysis of hy5/hyh Mutants
In this study, we minimized secondary expression changes in transcriptome analysis by choosing a developmental stage at which mutants and wild-type display minimal morphological differences, but the genes in question are known to be nevertheless active. Our approach revealed that about 2.7% of tested genes are consistently misexpressed in hy5 hyh, a number that is in the range of a previous experiment, although array types and biological material used are not comparable . One disadvantage of our strategy is that genes primarily affected at later stages of development are missed. For instance, the dark-grown seedlings used in this study had not yet developed lateral root primordia. This is presumably why, for instance, SOLITARY ROOT (SLR/IAA14), previously found to be misexpressed in hy5  and consistent with its role in lateral root emergence , is not affected in this study.
The total number of genes misexpressed in hy5 hyh is 627, with approximately two thirds underexpressed and one third overexpressed. Notably, HY5 and HYH do not possess transcription activation or repression domains and likely act in concert with other factors . Therefore, it is conceivable that they could repress the expression of some genes but activate the expression of others. It seems unlikely that all 627 genes are direct targets of HY5 and/or HYH. In general, the promoters of direct target genes would be expected to contain a HY5/HYH binding site, the G-box motif. One or more G-box motifs can be found in the 5′ 1,000-bp promoter regions of 97 genes (C. S. Hardtke, unpublished data). These include, for instance, CCA1, CHS, and CAB genes and a number of transcription factor genes (Table 1). Interestingly, among the auxin-responsive genes, G-box motifs are not more frequent than in the complete set of 627 genes (approximately 15% to 16%). Nevertheless, the proportion of auxin-responsive genes among the 627 genes affected in the double mutant (approximately 39%) significantly exceeds the proportion of auxin-responsive genes in the wild-type (approximately 16%). Thus, in line with the phenotypic analysis of hy5 hyh double mutants, HY5 and HYH clearly modulate auxin-regulated gene expression but most likely by controlling a few central regulators of auxin response. Among the functionally defined auxin signaling genes affected in the double mutant, only MSG2/IAA19 contains a G-box motif. Interestingly, as in AXR2/IAA7 and SLR/IAA14 , it is located close to the transcription initiation site. Consistent with hy5 and hy5 hyh phenotypes, MSG2/IAA19 has been implicated in hypocotyl growth responses and lateral root formation . Moreover, MSG2/IAA19 is a highly light-responsive gene that is expressed at very high levels in darkness and repressed upon light stimulus, a feature it shares with the equally affected SHY1/IAA6 gene . Thus, MSG2/IAA19 could represent one of the central auxin signaling components that directly link light- and auxin-induced gene expression.
Auxin Signaling versus Auxin Transport
While the transcriptome analyses demonstrate a perturbation of auxin signaling, it also appears possible that the hy5 and double mutant phenotypes rather result from altered auxin transport. For example, the reduced basipetal auxin transport is consistent with the agravitropism of hy5 roots and the increased acropetal transport with enhanced lateral root emergence. In general, however, it is difficult to determine whether the primary defect is in auxin transport or signaling, because of the inherent feedback connections between the two processes . Several observations favor the interpretation that altered auxin transport in hy5 hyh mutants is a secondary consequence of altered auxin signaling. For instance, root agravitropism and lateral root emergence defects of the axr4 auxin transport mutant can be rescued by application of the lipid-soluble auxin analog NAA [36,37]. This is, however, not the case for hy5 or the double mutant (C. S. Hardtke, unpublished data). Also, our naringenin feeding experiments exclude the possibility that auxin transport is altered because of reduced flavonoid biosynthesis, since naringenin treatment did not restore gravitropism in hy5 roots. In contrast, growth of flavonoid-deficient and agravitropic tt4 mutant seedlings on naringenin restores gravity response . Moreover, acropetal auxin transport is significantly enhanced to the same degree in hy5, hyh, and the double mutants, but their root branching phenotypes are very different. Finally, HY5 and HYH are transcription factors, but genes directly implicated in auxin transport are conspicuously absent from the set of genes with altered expression levels in the mutants. Therefore, the combined evidence suggests that hy5 and hy5 hyh mutants are mainly defective in the perception or interpretation of auxin stimulus (i.e., auxin signaling), and alterations in auxin transport are likely a secondary consequence of feedback regulation.
Auxin-Related Phenotypes in hy5 and hy5 hyh Mutants: A Quantitative Affair?
Our transcriptome analyses and the novel hy5 hyh shoot phenotypes support the hypothesis that auxin signaling is constitutively disturbed in hy5 and the double mutants. The transcriptome analyses also suggest that the molecular defects in hy5 and hy5 hyh are largely similar although quantitatively different. The number of misregulated auxin-responsive genes is higher in the double mutant than in hy5. Moreover, in the case of genes that are affected in both genotypes, the magnitude of misregulation is always considerably higher in the double mutant. Finally, the auxin-induction experiments clearly indicate that the vast majority of auxin-responsive genes that are affected in the double mutant are expressed at constitutively auxin-induced or -repressed levels. Therefore, in the microarray analyses, hy5 hyh mutants largely mimic auxin-treated wild-type, suggesting that auxin signaling is constitutively elevated. This is also true for hy5, albeit at a lower quantitative level.
The phenotypic progression from wild-type to hy5 to the double mutant correlates with quantitatively ever-increasing disturbance of auxin-responsive gene expression, reflecting ever-increasing constitutive auxin signaling. Thus, it appears that the smaller increase in constitutive auxin signaling in hy5 accelerates root system growth, while a further increase beyond a critical threshold, a situation created in the double mutant, suppresses growth (Figure 7).
Graphical presentation of a model explaining the opposite root system phenotypes of hy5 and hy5 hyh mutants. The strength of (constitutive) auxin signaling in the respective genotype determines the extent of root system growth. Root system growth is maximal at a certain optimum auxin signaling level but decreases if this level is either lower or higher. This assumption is supported by the phenotypic response of wild-type seedling root systems to the external application of increasing amounts of auxin: whereas low auxin concentrations promote root system growth, high concentrations inhibit growth.
In summary, we therefore conclude that the disparate root system growth phenotypes of hy5 and the double mutant reflect a morphological response to a quantitative gradient in the same molecular process, i.e., a gradual increase in constitutive auxin signaling. Finally, because practically all the classic auxin responses, from tropisms to lateral organ formation to cell elongation and proliferation, are impaired in hy5 hyh double mutant seedlings, we conclude that HY5 and HYH are important general negative regulators of the auxin signaling pathway, modulating its amplitude from embryogenesis throughout seedling development.
Materials and Methods
Phenotypic differences in measurements highlighted in the Results section are all statistically significant at p = 0.01 based on Student's t-test.
Plant material and tissue culture.
Seedlings were grown at 22 °C under constant illumination on culture medium (0.5× MS salts, 0.5 g/L MES, 1% sucrose, 0.9% agar [pH 5.8]) unless otherwise stated. Light intensity was approximately 100 μE. In all assays, the hy5-KS50 null allele, the hyh T-DNA insertion null allele, and the respective double mutant combination were analyzed in comparison to their wild-type background, Ws. In the auxin transport assays and microarray analyses, the hy5–215 null allele was compared to its background parent, Col.
Confocal analysis of roots.
To determine mature cell size and meristem size in the primary roots of the different genotypes, 7-d-old propidium iodide–stained seedlings were observed by confocal microscopy. For mature cell size, cortex cells were measured; for meristem size, proliferating cells in the meristematic zone were counted as described .
Physiological assays and phenotyping.
Morphological phenotypes were determined in tissue culture for at least 100 seedlings. Auxin transport assays, naringenin feeding experiments, and gravitropism assays were performed as described  with a minimum of 20 scored seedlings per treatment and genotype. For adventitious root induction, 12 or more 5-d-old etiolated plants were transferred into light and adventitious root emergence was monitored after 5 and 12 d.
Creation and analysis of transgenic plants.
Plasmids were created by amplification of HY5 or HYH promoter fragments (from 5′ to the ATG up to the neighboring gene) or ORFs from genomic or cDNA templates, respectively, with Pfu polymerase (Fermentas, http://www.fermentas.com), followed by cloning into binary vector pTCSH1  or its derivatives. Binary constructs were verified by sequencing and transformed into hy5–215 single mutant or hy5-KS50 hyh double mutant plants via floral dip using Agrobacterium. Transgenic lines were selected by screening seed progeny for glufosinate ammonium or hygromycin resistance on medium containing 0.3% sucrose. Independent lines segregating single locus insertions and stably expressing the transgenes in the T3 generation were chosen for analysis.
Light-to-dark shift experiments and detection of HYH proteins using anti-HYH antibody was performed as described .
Quantitative real-time RT-PCR.
Total RNA was isolated from seedlings, roots, or shoots (20 individuals) using the RNeasy kit with DNase step (Qiagen, http://www.qiagen.com). Reverse transcription (Promega, http://www.promega.com) was carried out according to the manufacturer's instructions using 1.5 μg of total RNA and oligo-dT primers. Samples were treated simultaneously. qPCR analyses were carried out on a Stratagene Mx3000P apparatus (http://www.stratagene.com) using SYBR green dye technology (http://www.bio-rad.com). PCR amplifications of 45 cycles were done in two-step reactions, with a denaturation of 10 s at 94 °C and an elongation of 2 min at 68 °C. Gel electrophoresis was systemically done to verify amplicons. Absolute quantity of transcripts was calculated using DNA standard curves . Results are presented in-fold change or absolute values, standardized in relation to the EF1 housekeeping gene. All qPCR data represent the average of two (CCA1, CUC1, ARGOS, IAA19) or three (HY5, HYH) independent biological and technical replicates. Primers used for CCA1 were GCCGCAGTAGAATCAGCTCCAATATAA and GAAGCATCTAATCCGATTCCAAGAA. Primers used for CUC1 were GCACGTGTCCTGTTTCTCCAATAA and ATCTGTCCCGATGATCCCAAA. Primers used for ARGOS were CGGAGTTTCTCGGCGCAGAAA and CAATGGGAACCAATAGCAGCATAAA. Primers used for IAA19 were GTCATGCAAGAGGTTGAGAATAA and AACTCAACACTCAAGAAACAAGTA. Primers used for altHYH were CCCACAAGAAGCACAAAACTGCTGGAT and CACGGCGGCGTTTAGCTGTAGAGA. Primers used for flHYH were CCCACAAGAAGCACAAAACTGAGGAAA and CTTCCACGGCGGCGTTTAGCTGTAGAGA. Primers used for HY5 were CCATCAAGCAGCGAGAGGTCATCAA and CGCCGATCCAGATTCTCTACCGGAA. Primers used for EF1 were GGTCACCAAGGCTGCAGTGAAGAA and GCTCAAACGCCATCAAAGTTTTAAGAA.
For microarray analysis, 20 or more 3-d-old etiolated seedlings grown on sugar-free medium were transferred into liquid medium and into the light. Plants were treated or mock-treated with 10 μM IAA after 5 h of light induction and harvested 1 h later. Total RNA was isolated using RNeasy kits (Qiagen) according to the manufacturer's instructions. Labeling and hybridization of ATH1 DNA arrays (22k) (Affymetrix) was performed according to the manufacturer's instructions (http://www.affymetrix.com/support/technicalmanual/expression_manual.affx). Intensity values were normalized with the MAS 5.0 method. Data were analyzed using the RACE software and the Bayes test for statistical significance . Variations in expression level were considered significant only if the fold change was greater than 2 with a probability lesser than or equal to 0.05. Two biological replicates were performed for all samples.
Table S1. List of All Genes Consistently Misregulated in hy5 hyh Double Mutants
The columns indicate the Affymetrix probe identifier, the Arabidopsis gene identifier, the gene description, and the expression ratios as indicated. dbl. indicates hy5 hyh double mutant.
(195 KB XLS)
Table S2. List of All Genes that Were Auxin Responsive in the Wild-Type and Their Response in the Mutant Genotypes
The columns indicate the Affymetrix probe identifier, the Arabidopsis gene identifier, the gene description, and the expression ratios as indicated. dbl. indicates hy5 hyh double mutant.
(88 KB XLS)
The raw data are available from the ArrayExpress database (http://www.ebi.ac.uk/arrayexpress) under accession number E-MEXP-715.
We would like to thank Profs. T. Berleth, C. Fankhauser, and L. Keller for helpful comments on the manuscript, and the DNA Array Facility of the University of Lausanne for assistance with microarray experiments.
RS contributed the data for Figures 1A–1P, 2, 3, 4, and 5. PS contributed the data for Figure 6. CH contributed the data for Figure 1Q and 1R. RS performed the microarray experiments and analyzed them together with CSH (Figure 5 and Tables 1 and S1). CSH and RS conceived this study and wrote the manuscript, with support from MH and GKM.
- 1. Chen M, Chory J, Fankhauser C (2004) Light signal transduction in higher plants. Annu Rev Genet 38: 87–117.M. ChenJ. ChoryC. Fankhauser2004Light signal transduction in higher plants.Annu Rev Genet3887117
- 2. Mas P (2005) Circadian clock signaling in Arabidopsis thaliana: From gene expression to physiology and development. Int J Dev Biol 49: 491–500.P. Mas2005Circadian clock signaling in Arabidopsis thaliana: From gene expression to physiology and development.Int J Dev Biol49491500
- 3. Oyama T, Shimura Y, Okada K (1997) The Arabidopsis HY5 gene encodes a bZIP protein that regulates stimulus-induced development of root and hypocotyl. Genes Dev 11: 2983–2995.T. OyamaY. ShimuraK. Okada1997The Arabidopsis HY5 gene encodes a bZIP protein that regulates stimulus-induced development of root and hypocotyl.Genes Dev1129832995
- 4. Holm M, Ma LG, Qu LJ, Deng XW (2002) Two interacting bZIP proteins are direct targets of COP1-mediated control of light-dependent gene expression in Arabidopsis. Genes Dev 16: 1247–1259.M. HolmLG MaLJ QuXW Deng2002Two interacting bZIP proteins are direct targets of COP1-mediated control of light-dependent gene expression in Arabidopsis.Genes Dev1612471259
- 5. Chory J, Reinecke D, Sim S, Washburn T, Brenner M (1994) A role for cytokinins in de-etiolation in Arabidopsis (det mutants have an altered response to cytokinins). Plant Physiol 104: 339–347.J. ChoryD. ReineckeS. SimT. WashburnM. Brenner1994A role for cytokinins in de-etiolation in Arabidopsis (det mutants have an altered response to cytokinins).Plant Physiol104339347
- 6. Fujioka S, Li J, Choi YH, Seto H, Takatsuto S, et al. (1997) The Arabidopsis deetiolated2 mutant is blocked early in brassinosteroid biosynthesis. Plant Cell 9: 1951–1962.S. FujiokaJ. LiYH ChoiH. SetoS. Takatsuto1997The Arabidopsis deetiolated2 mutant is blocked early in brassinosteroid biosynthesis.Plant Cell919511962
- 7. Kieber JJ (1997) The ethylene signal transduction pathway in Arabidopsis. J Exp Bot 48: 211–218.JJ Kieber1997The ethylene signal transduction pathway in Arabidopsis.J Exp Bot48211218
- 8. Neff MM, Nguyen SM, Malancharuvil EJ, Fujioka S, Noguchi T, et al. (1999) BAS1: A gene regulating brassinosteroid levels and light responsiveness in Arabidopsis. Proc Natl Acad Sci U S A 96: 15316–15323.MM NeffSM NguyenEJ MalancharuvilS. FujiokaT. Noguchi1999BAS1: A gene regulating brassinosteroid levels and light responsiveness in Arabidopsis.Proc Natl Acad Sci U S A961531615323
- 9. Vandenbussche F, Smalle J, Le J, Saibo NJ, De Paepe A, et al. (2003) The Arabidopsis mutant alh1 illustrates a cross talk between ethylene and auxin. Plant Physiol 131: 1228–1238.F. VandenbusscheJ. SmalleJ. LeNJ SaiboA. De Paepe2003The Arabidopsis mutant alh1 illustrates a cross talk between ethylene and auxin.Plant Physiol13112281238
- 10. Kim BC, Soh MC, Kang BJ, Furuya M, Nam HG (1996) Two dominant photomorphogenic mutations of Arabidopsis thaliana identified as suppressor mutations of hy2. Plant J 9: 441–456.BC KimMC SohBJ KangM. FuruyaHG Nam1996Two dominant photomorphogenic mutations of Arabidopsis thaliana identified as suppressor mutations of hy2.Plant J9441456
- 11. Tian Q, Reed JW (1999) Control of auxin-regulated root development by the Arabidopsis thaliana SHY2/IAA3 gene. Development 126: 711–721.Q. TianJW Reed1999Control of auxin-regulated root development by the Arabidopsis thaliana SHY2/IAA3 gene.Development126711721
- 12. Nagpal P, Walker LM, Young JC, Sonawala A, Timpte C, et al. (2000) AXR2 encodes a member of the Aux/IAA protein family. Plant Physiol 123: 563–574.P. NagpalLM WalkerJC YoungA. SonawalaC. Timpte2000AXR2 encodes a member of the Aux/IAA protein family.Plant Physiol123563574
- 13. Tatematsu K, Kumagai S, Muto H, Sato A, Watahiki MK, et al. (2004) MASSUGU2 encodes Aux/IAA19, an auxin-regulated protein that functions together with the transcriptional activator NPH4/ARF7 to regulate differential growth responses of hypocotyl and formation of lateral roots in Arabidopsis thaliana. Plant Cell 16: 379–393.K. TatematsuS. KumagaiH. MutoA. SatoMK Watahiki2004MASSUGU2 encodes Aux/IAA19, an auxin-regulated protein that functions together with the transcriptional activator NPH4/ARF7 to regulate differential growth responses of hypocotyl and formation of lateral roots in Arabidopsis thaliana.Plant Cell16379393
- 14. Tian CE, Muto H, Higuchi K, Matamura T, Tatematsu K, et al. (2004) Disruption and overexpression of auxin response factor 8 gene of Arabidopsis affect hypocotyl elongation and root growth habit, indicating its possible involvement in auxin homeostasis in light condition. Plant J 40: 333–343.CE TianH. MutoK. HiguchiT. MatamuraK. Tatematsu2004Disruption and overexpression of auxin response factor 8 gene of Arabidopsis affect hypocotyl elongation and root growth habit, indicating its possible involvement in auxin homeostasis in light condition.Plant J40333343
- 15. Cluis CP, Mouchel CF, Hardtke CS (2004) The Arabidopsis transcription factor HY5 integrates light and hormone signaling pathways. Plant J 38: 332–347.CP CluisCF MouchelCS Hardtke2004The Arabidopsis transcription factor HY5 integrates light and hormone signaling pathways.Plant J38332347
- 16. Holm M, Hardtke CS, Gaudet R, Deng XW (2001) Identification of a structural motif that confers specific interaction with the WD40 repeat domain of Arabidopsis COP1. EMBO J 20: 118–127.M. HolmCS HardtkeR. GaudetXW Deng2001Identification of a structural motif that confers specific interaction with the WD40 repeat domain of Arabidopsis COP1.EMBO J20118127
- 17. Osterlund MT, Hardtke CS, Wei N, Deng XW (2000) Targeted destabilization of HY5 during light-regulated development of Arabidopsis. Nature 405: 462–466.MT OsterlundCS HardtkeN. WeiXW Deng2000Targeted destabilization of HY5 during light-regulated development of Arabidopsis.Nature405462466
- 18. Seo HS, Yang JY, Ishikawa M, Bolle C, Ballesteros ML, et al. (2003) LAF1 ubiquitination by COP1 controls photomorphogenesis and is stimulated by SPA1. Nature 423: 995–999.HS SeoJY YangM. IshikawaC. BolleML Ballesteros2003LAF1 ubiquitination by COP1 controls photomorphogenesis and is stimulated by SPA1.Nature423995999
- 19. Hardtke CS, Gohda K, Osterlund MT, Oyama T, Okada K, et al. (2000) HY5 stability and activity in Arabidopsis is regulated by phosphorylation in its COP1 binding domain. EMBO J 19: 4997–5006.CS HardtkeK. GohdaMT OsterlundT. OyamaK. Okada2000HY5 stability and activity in Arabidopsis is regulated by phosphorylation in its COP1 binding domain.EMBO J1949975006
- 20. Ang LH, Chattopadhyay S, Wei N, Oyama T, Okada K, et al. (1998) Molecular interaction between COP1 and HY5 defines a regulatory switch for light control of Arabidopsis development. Mol Cell 1: 213–222.LH AngS. ChattopadhyayN. WeiT. OyamaK. Okada1998Molecular interaction between COP1 and HY5 defines a regulatory switch for light control of Arabidopsis development.Mol Cell1213222
- 21. Chattopadhyay S, Ang LH, Puente P, Deng XW, Wei N (1998) Arabidopsis bZIP protein HY5 directly interacts with light-responsive promoters in mediating light control of gene expression. Plant Cell 10: 673–683.S. ChattopadhyayLH AngP. PuenteXW DengN. Wei1998Arabidopsis bZIP protein HY5 directly interacts with light-responsive promoters in mediating light control of gene expression.Plant Cell10673683
- 22. Wang ZY, Tobin EM (1998) Constitutive expression of the CIRCADIAN CLOCK ASSOCIATED 1 (CCA1) gene disrupts circadian rhythms and suppresses its own expression. Cell 93: 1207–1217.ZY WangEM Tobin1998Constitutive expression of the CIRCADIAN CLOCK ASSOCIATED 1 (CCA1) gene disrupts circadian rhythms and suppresses its own expression.Cell9312071217
- 23. Xu Y, Johnson CH (2001) A clock- and light-regulated gene that links the circadian oscillator to LHCB gene expression. Plant Cell 13: 1411–1425.Y. XuCH Johnson2001A clock- and light-regulated gene that links the circadian oscillator to LHCB gene expression.Plant Cell1314111425
- 24. Aida M, Ishida T, Fukaki H, Fujisawa H, Tasaka M (1997) Genes involved in organ separation in Arabidopsis: An analysis of the cup-shaped cotyledon mutant. Plant Cell 9: 841–857.M. AidaT. IshidaH. FukakiH. FujisawaM. Tasaka1997Genes involved in organ separation in Arabidopsis: An analysis of the cup-shaped cotyledon mutant.Plant Cell9841857
- 25. Yang X, Lee S, So JH, Dharmasiri S, Dharmasiri N, et al. (2004) The IAA1 protein is encoded by AXR5 and is a substrate of SCF (TIR1). Plant J 40: 772–782.X. YangS. LeeJH SoS. DharmasiriN. Dharmasiri2004The IAA1 protein is encoded by AXR5 and is a substrate of SCF (TIR1).Plant J40772782
- 26. Hu Y, Xie Q, Chua NH (2003) The Arabidopsis auxin-inducible gene ARGOS controls lateral organ size. Plant Cell 15: 1951–1961.Y. HuQ. XieNH Chua2003The Arabidopsis auxin-inducible gene ARGOS controls lateral organ size.Plant Cell1519511961
- 27. Rashotte AM, Brady SR, Reed RC, Ante SJ, Muday GK (2000) Basipetal auxin transport is required for gravitropism in roots of Arabidopsis. Plant Physiol 122: 481–490.AM RashotteSR BradyRC ReedSJ AnteGK Muday2000Basipetal auxin transport is required for gravitropism in roots of Arabidopsis.Plant Physiol122481490
- 28. Buer CS, Muday GK (2004) The transparent testa4 mutation prevents flavonoid synthesis and alters auxin transport and the response of Arabidopsis roots to gravity and light. Plant Cell 16: 1191–1205.CS BuerGK Muday2004The transparent testa4 mutation prevents flavonoid synthesis and alters auxin transport and the response of Arabidopsis roots to gravity and light.Plant Cell1611911205
- 29. Hamann T, Mayer U, Jurgens G (1999) The auxin-insensitive bodenlos mutation affects primary root formation and apical-basal patterning in the Arabidopsis embryo. Development 126: 1387–1395.T. HamannU. MayerG. Jurgens1999The auxin-insensitive bodenlos mutation affects primary root formation and apical-basal patterning in the Arabidopsis embryo.Development12613871395
- 30. Hardtke CS, Berleth T (1998) The Arabidopsis gene MONOPTEROS encodes a transcription factor mediating embryo axis formation and vascular development. EMBO J 17: 1405–1411.CS HardtkeT. Berleth1998The Arabidopsis gene MONOPTEROS encodes a transcription factor mediating embryo axis formation and vascular development.EMBO J1714051411
- 31. Vroemen CW, Mordhorst AP, Albrecht C, Kwaaitaal MA, de Vries SC (2003) The CUP-SHAPED COTYLEDON3 gene is required for boundary and shoot meristem formation in Arabidopsis. Plant Cell 15: 1563–1577.CW VroemenAP MordhorstC. AlbrechtMA KwaaitaalSC de Vries2003The CUP-SHAPED COTYLEDON3 gene is required for boundary and shoot meristem formation in Arabidopsis.Plant Cell1515631577
- 32. Aida M, Ishida T, Tasaka M (1999) Shoot apical meristem and cotyledon formation during Arabidopsis embryogenesis: Interaction among the CUP-SHAPED COTYLEDON and SHOOT MERISTEMLESS genes. Development 126: 1563–1570.M. AidaT. IshidaM. Tasaka1999Shoot apical meristem and cotyledon formation during Arabidopsis embryogenesis: Interaction among the CUP-SHAPED COTYLEDON and SHOOT MERISTEMLESS genes.Development12615631570
- 33. Fukaki H, Nakao Y, Okushima Y, Theologis A, Tasaka M (2005) Tissue-specific expression of stabilized SOLITARY-ROOT/IAA14 alters lateral root development in Arabidopsis. Plant J 44: 382–395.H. FukakiY. NakaoY. OkushimaA. TheologisM. Tasaka2005Tissue-specific expression of stabilized SOLITARY-ROOT/IAA14 alters lateral root development in Arabidopsis.Plant J44382395
- 34. Zimmermann P, Hirsch-Hoffmann M, Hennig L, Gruissem W (2004) GENEVESTIGATOR. Arabidopsis microarray database and analysis toolbox. Plant Physiol 136: 2621–2632.P. ZimmermannM. Hirsch-HoffmannL. HennigW. Gruissem2004GENEVESTIGATOR. Arabidopsis microarray database and analysis toolbox.Plant Physiol13626212632
- 35. Leyser O (2006) Dynamic integration of auxin transport and signalling. Current Biology 16: R424–433.O. Leyser2006Dynamic integration of auxin transport and signalling.Current Biology16R424433
- 36. Dharmasiri S, Swarup R, Mockaitis K, Dharmasiri N, Singh SK, et al. (2006) AXR4 is required for localization of the auxin influx facilitator AUX1. Science 312: 1218–1220.S. DharmasiriR. SwarupK. MockaitisN. DharmasiriSK Singh2006AXR4 is required for localization of the auxin influx facilitator AUX1.Science31212181220
- 37. Yamamoto M, Yamamoto KT (1999) Effects of natural and synthetic auxins on the gravitropic growth habit of roots in two auxin-resistant mutants of Arabidopsis, axr1 and axr4: Evidence for defects in the auxin influx mechanism of axr4. J Plant Res 112: 391–396.M. YamamotoKT Yamamoto1999Effects of natural and synthetic auxins on the gravitropic growth habit of roots in two auxin-resistant mutants of Arabidopsis, axr1 and axr4: Evidence for defects in the auxin influx mechanism of axr4.J Plant Res112391396
- 38. Mouchel CF, Briggs GC, Hardtke CS (2004) Natural genetic variation in Arabidopsis identifies BREVIS RADIX, a novel regulator of cell proliferation and elongation in the root. Genes Dev 18: 700–714.CF MouchelGC BriggsCS Hardtke2004Natural genetic variation in Arabidopsis identifies BREVIS RADIX, a novel regulator of cell proliferation and elongation in the root.Genes Dev18700714
- 39. Rutledge RG, Cote C (2003) Mathematics of quantitative kinetic PCR and the application of standard curves. Nucleic Acids Res 31: e93.RG RutledgeC. Cote2003Mathematics of quantitative kinetic PCR and the application of standard curves.Nucleic Acids Res31e93
- 40. Psarros M, Heber S, Sick M, Thoppae G, Harshman K, Sick B (2005) RACE: Remote Analysis Computation for gene Expression data. Nucleic Acids Res 33: W638–W643.M. PsarrosS. HeberM. SickG. ThoppaeK. HarshmanB. Sick2005RACE: Remote Analysis Computation for gene Expression data.Nucleic Acids Res33W638W643