Plants are unique in their ability to continuously produce new meristems and organ primordia. In Arabidopsis, the transcription factor LEAFY (LFY) functions as a master regulator of a gene network that is important for floral meristem and organ specification. UNUSUAL FLORAL ORGANS (UFO) is a co-activator of LEAFY and is required for proper activation of APETALA3 in the floral meristem during the specification of stamens and petals. The ufo mutants display defects in other parts of the flower and the inflorescence, suggestive of additional roles. Here we show that the normal determinacy of the developing Arabidopsis leaves is affected by the expression of a gain-of-function UFO fusion protein with the VP16 transcriptional activator domain. In these lines, the rosette and cauline leaf primordia exhibit reiterated serration, and upon flowering produce ectopic meristems that develop into flowers, bract leaves and inflorescences. These striking phenotypes reveal that developing leaves maintain the competency to initiate flower and inflorescence programs. Furthermore, the gain-of-function phenotypes are dependent on LFY and the SEPALLATA (SEP) MADS-box transcription factors, indicative of their functional interactions with UFO. The findings of this study also suggest that UFO promotes the establishment of the lateral meristems and primordia in the peripheral zone of the apical and floral meristems by enhancing the activity of LFY. These novel phenotypes along with the mutant phenotypes of UFO orthologs in other plant species suggest a broader function for UFO in plants.
Citation: Risseeuw E, Venglat P, Xiang D, Komendant K, Daskalchuk T, Babic V, et al. (2013) An Activated Form of UFO Alters Leaf Development and Produces Ectopic Floral and Inflorescence Meristems. PLoS ONE 8(12): e83807. doi:10.1371/journal.pone.0083807
Editor: David E. Somers, Ohio State University, United States of America
Received: March 26, 2013; Accepted: November 9, 2013; Published: December 23, 2013
Copyright: © 2013 Risseeuw 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 supported by Genome Canada, National Research Council publication number 50141. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
The continuous production of new meristems is a characteristic feature in plants and accounts for their distinctive indeterminate growth. After germination, the shoot apical meristem (SAM) produces phytomers repetitively which represent an internodal stem with a node comprising of a leaf subtending an axillary meristem . The apical and axillary meristems are usually indeterminate , whereas the leaf primordia are most often determinate . During the course of its life cycle, the plant produces multiple meristems and primordia and these will acquire different identities to give rise to different organs. The meristems can switch identity over time and this is particularly important during the transition from the vegetative to the reproductive phase. The identities are determined by the combinatorial expression and functions of specific meristem and organ identity genes controlled spatially and temporally by preprogrammed genetic networks . In Arabidopsis, the LEAFY (LFY) protein is a master regulator of the organ identity genes and its function is essential for both conferring floral meristem identity and the subsequent identity of the individual floral organs. LFY is a plant specific transcription factor and activates several key floral organ identity genes including the ABC class MADS-box genes . The lfy mutant is impaired in the floral fate specification of the meristems produced by the inflorescence meristem, and as a consequence, new meristems default towards a co-inflorescence fate, resulting in a leafy appearance , .
UNUSUAL FLORAL ORGANS (UFO) is a key cofactor of LFY to specify the petal and stamen whorls by regulating the expression of the B-class MADS-box gene APETALA 3 (AP3) in the floral meristem , , . Therefore in ufo flowers, petal and stamen development is severely affected resulting in either reduction or complete absence of these organs . The ufo mutant is also associated with a range of additional defects outside the AP3 expression domain including the loss of carpels in some flowers; replacement of flowers by filaments; and perturbed transition of the apical meristem from the vegetative to the inflorescence identity, particularly under short day conditions . These findings suggest that the spatial and temporal overlap of the LFY and UFO expression domains are important for specification of the floral meristem and the floral organ primordia . Compared to Arabidopsis, the expression domains of the LFY and UFO orthologs vary considerably in other plant species . Accordingly their individual functions and their respective mutant phenotypes are quite different from the Arabidopsis lfy and ufo mutants. For example, the UFO ortholog double top (dot) mutant in petunia is unable to produce flowers, whereas in the pea unifoliata (uni) and stamina pistilloida (stp) mutants, the orthologs of LFY and UFO, show reduced leaf complexity in addition to inflorescence abnormalities , . Though ufo mutants do not affect the leaf shape in Arabidopsis, the ectopic expression of UFO results in serrated leaves . These phenotypes indicate that the function of UFO and its homologs in other species are not restricted only to the specification of the petal and stamen whorls, but also extended to include other meristems and primordia both inside and outside of the floral program.
UFO belongs to a large group of F-box proteins encoded by a family of over 700 genes in Arabidopsis , . F-box proteins confer specificity to the SCF (Skp1-cullin-F-box complex) class of ubiquitin ligases by binding and presenting specific target proteins to the ubiquitin conjugating enzyme . The UFO F-box domain is required for the interaction with the Skp1 adapter protein (ASK proteins in Arabidopsis) and the COP9 signalosome , . The C-terminal domain of UFO has been shown to bind LFY and this interaction likely leads to its ubiquitination , . Transcription factors are often substrates for ubiquitination where this modification plays a dual role by activation followed by their turnover , , , . Therefore, UFO plays a unique role in flower development by ubiquitinating the plant specific transcription factor, LFY, which likely also requires the participation of UFO in the transcriptional complex . In this study, the involvement of UFO in a transcriptional complex was tested by the construction of activator and repressor versions of UFO employing the well characterized and widely used heterologous VP16 based activator and Engrailed based repressor domains respectively. The developmental effects produced by these overexpression constructs were evaluated in transgenic Arabidopsis, Brassica napus and tobacco plants. Our results showed that especially the activator fusion had a dramatic effect on the UFO gain-of-function phenotypes that include development of ectopic flowers and inflorescences subtended by bracts on Arabidopsis leaves. Analysis of these novel leaf phenotypes revealed potential functions of UFO outside the flower context. Additionally, comparison of UFO functions with its orthologs in other plant species also suggests a broader role for UFO during meristem establishment and specification.
UFO is a transcriptional co-activator
To assess the functions of UFO, Arabidopsis plants were transformed with the UFO gene under the control of the cauliflower mosaic virus 35S (CaMV 35S) promoter. 22% of the transgenic plants produced serrate leaves and flowers with reduced sepals and abnormalities in the development of the gynoecium valves and the style. Overall these plants displayed relatively milder phenotypes than the 35S:UFO phenotypes reported by Lee et al (Table S1; Figure 1B) . Expression of UFO under the control of the LFY promoter also resulted in serrated leaves, but occurred less frequently among the T1 transgenic lines (4%) compared to the expression with the 35S promoter (22%), suggesting that higher UFO levels were also required for the overexpression phenotypes (Table S1). When UFO was over-expressed in the sgs2-1 background, which suppresses gene silencing , all T1 plants showed the gain-of-function phenotypes with enhanced leaf serration (Table S1). These results suggest that the p35S:UFO plants (78%) with a weak and medium loss-of-function phenotypes in the wild type background were the result of partial silencing of the endogenous UFO gene and that high UFO levels were required for the observed leaf serration and other phenotypic changes (Table S1).
(A-L) Interaction with ASK1 is required for the nuclear function of UFO. (A–F) Phenotypes of Arabidopsis flowers from WT (A) compared with flowers from the following transgenic lines; p35S:UFO showing abnormal development of the gynoecium and the style (B); ask1-1 (C) and ufo-1 (D) showing fewer stamens; ask1-1 p35S: UFO showing normal gynoecium development (E); p35S:UFOdelF with weak, medium and strong ufo-1 mutant-like phenotypes (F). (G, H) Transient expression of p35S:YFP (G) and p35S:UFO-YFP (H) in Nicotiana benthamiana epidermal cells. Accumulation of UFO-YFP in the nucleus; (I–L) Respective uninduced controls (I,J) and dexamethasone induced (K,L) Arabidopsis plants and their flowers expressing UFO-GR. Nuclear translocation of the UFO glucocorticoid receptor fusion in the presence of dexamethasone resulted in leaf serration and floral defects reminiscent of the plants transformed with p35S:UFO (B). (M–S) UFO fusions with the engrailed (En) transcriptional repressor domain and with the VP16 transactivator domain. (M) p35S:En-UFO and (N) p35S:En-UFOdelF flowers showing strong phenotype. (O–Q) 3 week-old rosette plants of WT (O), p35S:UFO-VP16 showing medium (P) and strong (Q) phenotypes. Arrows indicate delayed leaf expansion. (R) p35S:UFO-VP16 in sgs2-1 mutant background showing strong phenotype with proliferative rosette leaves (R). A close up of the ectopic floral organs formed on the leaf tip is shown in (S).
Flowers of the ask1-1 mutant showed fewer petals compared to wild type and were often replaced with petal-stamen chimeras, which resemble the flowers of an intermediate ufo-1 mutant implying a genetic interaction between these two genes (Figure 1C, D) , . Accordingly, the interaction of UFO with the most abundant ASK1 protein  was required for the 35S:UFO phenotype because the ask1-1 mutation was epistatic to the UFO transgene (Figure 1E) and over-expression of UFO carrying a mutation in the F-box resulted in a weak ufo dominant-negative phenotype (Figure 1F). These phenotypes are also consistent with the paradoxical “activation by destruction” model which has been implicated for LFY . This model predicts that ubiquitination of transcription factors results in simultaneous activation and priming for destruction. Thus, UFO lacking the F-box domain is expected to stabilize un-ubiquitinated LFY and thereby repressing its activity. UFO is predominantly a nuclear protein as shown by the accumulation of a UFO-YFP fusion in the nucleus upon transient expression in Nicotiana benthamiana leaves (Figure 1G, H). This result also confirmed that translocation of UFO into the nucleus is required for its activity because fusion to the glucocorticoid receptor (GR), which is known to be retained in the cytosol in the absence of hormone, is unable to induce a gain-of-function phenotypes (Table S1; Figure 1 I, J). As expected, dexamethasone (DEX) induced translocation of UFO-GR from the cytosol into the nucleus, correlated with the initiation of serrated leaves and abnormal flowers in 23% of the transgenic lines (Table S1; Figure 1K, L). Taken together, the results showed that the function of UFO depends on its nuclear localization and its interaction with ASK1.
LFY is a key transcription factor in flower development and has been identified as a likely substrate for ubiquitination by UFO . Because UFO does not contain any known DNA binding domains, we reasoned that UFO likely functions in the context of a transcriptional complex that includes LFY. In this situation, the fusion of UFO to the Drosophila Engrailed (En) transcriptional repressor domain or to the viral VP16 activator domain was expected to influence the function of this putative transcriptional complex in a dominant negative (loss-of-function) and a dominant (gain-of-function) manner respectively. This was indeed the case and the strong novel phenotypes identified in this study further indicate potential additional roles for UFO in plant development.
When the En-UFO translational fusion was over-expressed in Arabidopsis under the 35S promoter, ~85% of the T1 plants exhibited a range of mild to strong ufo-1 like phenotypes with normal leaves. Overall these phenotypes were stronger compared to the plants expressing UFO without the F-box, but weaker than the reported UFO-SRDX fusion (Table S1; Figure 1M) . Upon combining the Engrailed domain with the F-box deletion, more T1 transgenic plants showed strong loss-of-function phenotypes with flowers containing sepal-petal, stamen-carpel chimera or filaments in the second and third whorl or flower-filament substitutions in the inflorescence (Table S1; Figure 1N). In contrast, every T1 plant expressing the UFO-VP16 fusion exhibited leaf serration (Figure 1P, Q), which was more severe compared to plants over-expressing UFO only. RT-PCR analysis revealed an 8-fold increase in the UFO-VP16 transcript levels compared to endogenous UFO RNA consistent with the observed phenotypes (Figure S1; see Methods). Based on the onset and severity of the leaf serration, the transgenic lines could be divided into two groups. About 86% of the plants showed clear serration starting in the third or fourth true leaf and these were designated as the weak and medium phenotype group whereas the plants in the strong phenotype group showed serration of all rosette leaves (Table S1; Figure 1P, Q). Compared to wild type and 35S:UFO transgenic plants, the emergence of the first true leaves was delayed in UFO-VP16 expressing lines, especially in the plants that showed strong gain-of-function phenotypes. The serrations became increasingly severe in later formed leaves. When UFO-VP16 was expressed in the sgs2-1 background, all T1 plants from the weak and medium phenotype group displayed a strong gain-of function phenotype, indicating that the weaker phenotype was caused by either lower UFO-VP16 protein expression and/or by partial silencing of the endogenous UFO gene (Table S1; Figure 1R, S). The result that the VP16 transcriptional activator and not the En repressor enhanced the UFO over-expression phenotype suggests that UFO likely functions as a transcriptional co-activator.
UFO-VP16 causes flowering leaves
Overexpression of UFO fused to the VP16 transactivation domain resulted in unexpected phenotypes not observed in the earlier studies. 50% of the T1 plants, which belonged to the first group developed flowers along the adaxial edge beginning in the last three rosette leaves that are formed prior to bolting and later in all the cauline leaves (Figure 2A–C). These floral meristems were ectopic because they were neither derived from the apical meristem nor from the displacement of the axillary meristem. Although most of the leaf blade originated from the basal part of the leaf, the flowering rosette leaves often grew to a normal size. Sometimes the flowers were also subtended by a bract leaf (Figure 2D). Occasionally an inflorescence would develop in addition to the individual flowers (Figure 2E). These flowers were mostly male sterile, but produced viable seeds upon pollination (Figure 2F). Closer examination revealed that the lower rosette leaf primordia had serrations along their margins that became compounded at later stages as shown by secondary serrations (Figure 2G, H). These leaf primordia exhibited a prolonged primordial phase and eventually developed into severely lobed leaves that were covered with enlarged trichomes (Figure 2J). The upper rosette leaf primordia that were formed during floral transition were also serrated and initiated floral meristems that developed in a sequential acropetal fashion along the adaxial margins (Figure 2K–N). It is interesting to note that each developing floral meristem (indicated by red arrow in Figure 2M, N) was positioned at the distal end of a serration (indicated by yellow star in Figure 2M, N), and few of them formed bract-like structures (Figure 2D). These ectopic floral meristems followed the normal developmental progression as defined by the stages shown in the insets of Figures 2K,O–Q . The floral meristems on the leaves developed into complete flowers including the pedicel, and were similar to the flowers produced on the main inflorescence. Often these ectopic floral meristems were fused to produce fasciations of the pedicel or of the flowers themselves. Few of these ectopic meristems developed into inflorescence meristems that produced flowers along their flanks (Figure 2M, 2E). These phenotypes indicate that the inflorescence program, which is normally established in the axis of the leaf, now expanded into the leaf primordium during its extended meristematic phase.
(A–D) Upper rosette leaves of p35S:UFO-VP16 plant (A) with ectopic flowers (B; C-close-up), occasionally subtended by an ectopic bract (D). (E–F) Ectopic inflorescences on the rosette leaves of p35S:UFO-VP16 plants (E) that produce siliques (F) and fertile seeds upon pollination (inset in F). (G–N) Ontogeny of the ectopic flower/inflorescence formation on the leaves of p35S:UFO-VP16 plants. Developing lower rosette leaf primordia showing serrations along the margins (G) that produce secondary serrations (arrows) at a later stage (H). Developing upper rosette leaves of WT (I) and p35S:UFO-VP16 (J–Q); rosette leaf prior to flowering showing deep serrations and an excess of enlarged trichomes (J); serrated rosette leaves formed at flowering with ectopic floral/inflorescence meristems (K–Q) that show progressive floral developmental stages (insets in K, O–Q). Grey boxed regions in K and L are magnified in M and N; red arrows indicate the emerging floral primordia that are positioned at distal ends of the serrations (yellow stars). Green stars in J–L, O–Q indicate axillary meristems. Bar = 1 mm (I, J); 0.1 mm (G, H, K–Q).
After the floral transition, the cauline leaves surrounding the apical inflorescence meristem also initiated ectopic floral meristems that covered most of the leaf blade (Figure 3A–D). These floral meristems were positioned in close proximity to the axillary co-inflorescences resulting in the fasciation of the peduncle of the co-florescence and the petiole of the subtending flowering cauline leaf (Figure 3C, E).Similar to plants expressing UFO without VP16, flowers of the first group had mostly a normal organ number but the sepals were wrinkled and the petals, stamens and carpels were stunted (Figure 3F). However, the UFO-VP16 plants with a strong phenotype belonging to the second group exhibited a more disorganized inflorescence that was delayed in development (Figure 3G). The cauline leaf primordia initiated floral meristems as observed in the first group with weaker phenotype, but remained meristematic and failed to progress into normal flowers (Figures 1S, 3I bottom panel). The flowers on the primary inflorescence were clustered due to very short pedicels and delayed internodal elongation of the peduncle (Figure 3H, I). The flowers had serrated petal-sepal chimeric organs in the first whorl and the gynoecium was either incompletely fused or replaced by additional stamens (Figure 3J). Plants transformed with p35S:UFOdelF-VP16, that lacked a functional F-box domain failed to produce the above described UFO-VP16 gain-of-function phenotypes and instead showed a loss-of-function phenotype similar to p35S:UFOdelF without VP16 (Table S1, Figure 3K). These results further confirmed that F-box domain of UFO is required for VP16 mediated gain-of-function phenotypes.
(A–F) p35S:UFO-VP16 inflorescence with a medium phenotype showing the developing flowers (outlined in red) produced by the primary inflorescence meristem (red star) (A - top view, B - side view) and by the cauline leaves (blue star) shown at different developmental stages (A–E); the developing co-florescence meristem (green star) and the transformed cauline leaf primordium (C) fail to separate leading to a fasciated structure (E); flowers show reduced and short petals, stamens and carpels (F). (G–J) p35S:UFO-VP16 inflorescence with a strong phenotype showing an disordered inflorescence meristem (red star) with delayed development of the floral primordia (G) that eventually bolts to produce flowers (H) with serrated floral organs and short pedicels (I-top panel, J) and cauline leaves (blue star) with ectopic disordered floral meristems (G) that develop into abnormal flowers (I-bottom panel). (K) p35S:UFOdelFVP16 flowers with a medium ufo-1 like phenotype. Bar = 0.1 mm (A-D, G).
Meristem specification by UFO in other plant species
Transformation of the related crucifer Brassica napus with p35S:UFO-VP16 resulted in severe serration of the leaves in addition to the lobing observed in wild type leaves (Figure 4A–D, Table S1). These serrations were compounded as a result of reiterated serrations during leaf development (Figure 4D). Closer examination of a young leaf showed a highly meristematic leaf margin, which likely contributed to these progressively increased leaf serrations in the older leaves (Figure 4E, F). The sinus regions of these leaves often remained meristematic producing new projections for a prolonged period (Figure 4C inset). Though, expansion of the leaves was delayed, the size of the mature leaves often surpassed that of the wild type plants. Similar to Arabidopsis, the cauline leaf blade was consumed by proliferating ectopic floral structures (Figure 4G, I). The weaker p35S:UFO-VP16 lines showed meristematic cauline leaf margins without ectopic floral meristems (Figure 4H, J). The flowers produced by the primary inflorescence in the weaker lines were clustered without sufficient elongation of the internodes and with shorter pedicels whereas in the stronger lines, a mass of proliferating floral organs was produced (Figure 4G, H). Taken together, though some differences were observed, the p35S:UFO-VP16 mediated gain-of-function phenotypes of B. napus were comparable to that of Arabidopsis.
Wild type plant (A) showing normal lobed leaves (B). (C–F) p35S:UFO-VP16 plant (C) showing severe lobing of the leaf (D); expanding young leaf (E) showing meristematic activity along the leaf margin (F) that leads to the enhanced lobing. Inset in (C) shows prolonged meristematic activity of the leaf margin. (G–J) Inflorescences of p35S:UFO-VP16 plants showing severe proliferation of floral organs produced by the inflorescence meristem (G) and by the cauline leaves (G, I; white arrows); weaker phenotype showing the development of modified flowers with short pedicels (H) and prolonged meristematic activity of the cauline leaf margins (H, J).
To determine whether UFO could induce similar phenotypes in more unrelated plant species, the UFO constructs were transformed into tobacco (Nicotiana tabacum). In the tobacco cymose inflorescence, the apical inflorescence meristem and the consecutive co-infloresences terminate in a flower, whereas in the crucifers i.e., Arabidopsis and B.napus, the indeterminate racemose inflorescence produces flowers in an acropetal fashion. Tobacco plants over-expressing UFO produced light green sectors starting in the third leaf as well as more curling of the margins compared to wild type (Figure 5A, B; Table S1). The cellular organization of these light green sectors in the cross sections showed high similarity with sepals as opposed to leaves of wild type plants (Figure 5K–M). Pink pigmented sectors were also present occasionally in the upper leaves (Figure 5E), indicative of the chimeric nature of the vegetative leaves mixed with characteristics of sepal and petal cell types. The severity of the leaf phenotype correlated with earlier flowering, on average 57 days after seeding in p35S:UFO plants versus more than 90 days in wild type. The typical whorled phyllotaxy of wild type tobacco flowers was absent in the UFO over-expression lines (Figure 5F–I). Instead, the flowers exhibited a continuum of the spiral phyllotaxy of the shoot where the distinct floral whorls seen in wild type were replaced by a gradient of organ mosaics starting from cauline leaves that continued into sepal-cauline leaves, sepals, sepal-petals, petals, petal-stamens and stamens (Figure 5F-H). The UFO-VP16 tobacco plants flowered very early (~41 days after seeding) after producing about 5 leaves (Figure 5C); leaf curling and mosaics started in the second leaf but no ectopic floral meristems developed (Figure 5J). Taken together, UFO overexpression in tobacco had a distinct phenotypic effect compared to that observed in B.napus and Arabidopsis, highlighting the dependence of ectopic UFO or UFO-VP16 on the existing developmental programs and the associated genetic factors in these species.
(A–C) 6 week-old tobacco plants of WT (A), p35S:UFO (B) and p35S:UFO-VP16 at vegetative, bolting and flowering stages respectively. (D–H) p35S:UFO plant showing light green sepal-like (D) and pink petal-like (E) sectors in the vegetative leaves; flowers with spiral phyllotaxy of the sepal, petal and stamen whorls showing stamen [s], petal-stamen [pst], petal [p], petal-sepal [ps], sepal [s] and sepal-cauline leaf [sc] subtending a co-florescence [cf] (F–H); the flower in (F) shows a split corolla; the mature flower in (H) has shed its petals and stamens and shows a developing pod. (I) Wild type flower. (J) 8 week-old p35S:UFO-VP16 showing abnormal leaves and early flowering. (K–M) Cross sections of a wild type leaf (K), a sepal (L), and a light green sector of a p35S:UFO vegetative leaf (M). The palisade (pm) and spongy (sm) mesophyll layers seen in the leaf are not present in the sepals and in the modified p35S:UFO leaf sectors. Bar = 0.1 mm.
UFO function depends on both LFY and SEP proteins
Floral meristems of the lfy-1 mutant default into a secondary co-florescence identity and are unable to develop a gain-of-function phenotype when UFO is overexpressed , . The dependence of UFO on LFY was also observed in the present study with UFO-VP16 as the lfy-1 mutant was fully epistatic to the UFO-VP16 transgene (Figure 6A–C). Expression of the pLFY:GUS reporter in p35S:UFO-VP16 plants was similar to its expression in the wild type background (Figure 6D, E). Upon flowering, the GUS activity was strong in the shoot apex and leaf primordia of both lines, but was not detected in the emerging leaves. Also, LFY RNA levels of wild type and p35S:UFO-VP16 seedlings were similar as determined by RT-PCR (Figure S1). These results suggest that the LFY expression was not upregulated by UFO-VP16, and the observed phenotypes were more likely the result of a prolonged interaction between UFO-VP16 and LFY during the early stages of leaf development (see discussion).
Inflorescence of lfy-1 (A) compared to that of lfy-1 p35S:UFO-VP16 (B). Normal rosette of lfy-1 p35S:UFO-VP16 (C). (D, E) GUS expression of a pLFY:GUS in wild type (D) and p35S:UFO-VP16 (E) seedling. (F) pAP1:GUS p35S:UFO-VP16 seedling with GUS expression in the primary leaves. (G) AP3:GUS p35S:UFO-VP16 shoot apex after evocation with GUS expression appearing in the leaves. (H) ap1-10 p35S:UFO-VP16 cauline leaf with ectopic ap1 like flowers. (I-Q) sep mutants compared with their corresponding sep UFO-VP16 transgenic lines: (I-K) sep1 sep2-1 sep3-2 sep4-1/+; (L–M) sep1 SEP2-1rev/rev sep3-2/+ sep4-1; and (O-Q) sep1 sep2-1 sep3-2/+ SEP4. Control flowers (I, L, O); flowers (J, M, P) and rosettes (K, N, Q) of mutants transformed with UFO-VP16 transgene. sep2-1 carries an En-1 insertion in the seventh intron, which has excised in the SEP2-1rev revertant allele. Flowers with bract-like organs (I,J) and a normal rosette (K); normal flowers (L,M) and rosette (N): normal flower (O) and UFO-VP16 like flowers that have short pedicels with a flowering cauline leaf (arrow, P); UFO-VP16 like rosette (Q). (R) p35S:SEP1 inflorescence terminating in a flower. (S, T) p35S:SEP4-VP16 rosette with leaves showing serration (S) and inflorescence producing flowers with short pedicels (T).
Next we tested whether UFO-VP16 is involved in the regulation of the targets of LFY that include A, B, C and E class MADS-box genes . Our results showed that pAPETALA1:GUS was expressed earlier in the lower leaves of UFO-VP16 seedlings prior to flowering, whereas pAPETALA3:GUS was detected only in the upper serrated leaves at flowering stage (Figure 6F, G). No ectopic expression was observed with the APETALA3, PISTILLATA and AGAMOUS promoters prior to flowering (not shown). These observations are consistent with the result that none of the ABC mutants were able to suppress the serrated leaf phenotype and the flowers on both the inflorescence and the leaves retained the characteristics from the non-transformed mutants. Interestingly, serration was enhanced in the ap1 mutant and the ectopic meristems on the leaves developed into ap1-like flowers (Figure 6H). These observations suggest that the ABC class MADS box genes were not required for the gain-of-function leaf phenotypes.
MADS-box proteins function in quaternary complexes to regulate the identity of the meristems and primordia in the above-ground region of the plant . Generally at least one position in the complex is taken by a member of the four SEPALLATA MADS-box proteins (SEP1, SEP2, SEP3, SEP4), to mediate the formation of higher-order complexes . Because the SEP proteins function in a partially redundant manner, the UFO-VP16 construct was transformed into fertile sep1/sep1,sep2/sep2,SEP3/sep3,SEP4/sep4 plants using the flower dip method and analyzed in the segregating offspring. The majority of 36 sep UFO-VP16 T1 plants (24 plants) did not show leaf serration, indicating that some combinations of the sep alleles had suppressed the gain-of function phenotype, but instead showed flower phenotypes similar to the respective sep mutants without the transgene (Figure 6I–N). The second group (12 plants) showed various levels of serration, including 5 with ectopic flowers on the leaves and flowers typical for UFO-VP16 (Figure 6O–Q). Genotyping of the segregating plants for the 4 SEP genes (see methods) revealed that the sep mutant alleles in various combinations were sufficient to suppress the UFO-VP16 phenotype of the first group. All plants with one wild type SEP allele and seven out of eight plants with two SEP alleles belonged to the first group, showing a positive correlation between the UFO-VP16 phenotype and the presence of a higher number of wild type SEP alleles. Furthermore, all seven plants carrying both SEP4 alleles had serrated leaves including five carrying ectopic flowers, indicating that SEP4 was required and is more critical than the other SEP proteins for this gain-of-function leaf phenotype. RT-PCR analysis revealed no differences in SEP transcript levels between UFO-VP16 and wild type seedlings (Figure S1) suggesting that higher expression levels of the SEP genes were not required. Taken together, these results suggest that in addition to LFY, the SEP proteins were also required for UFO gain-of-function phenotypes in Arabidopsis.
To test whether over-activation of SEP could result in similar phenotypic changes as observed in UFO transgenic plants, VP16 based activation constructs were developed with SEP1 and SEP4. SEP4-VP16 over-expressing plants exhibited mild serration of the leaves, which often curled up at the edges (Table S1, Figure 6S). No ectopic meristems were observed on the leaves. However the flowers were strikingly similar to those observed in UFO-VP16 plants. The pedicels were short and the growth of the peduncle was delayed giving the inflorescence a compact appearance (Figure 6T). Further, the development of the flower buds was delayed for an extended period. Plants with a weak phenotype were taller with uneven internodal distances between the flowers. A similar weak phenotype was observed in plants transformed with SEP1-VP16. Both transgenics flowered at normal times, which contrasted with the very early flowering of p35S:SEP1 transgenics and prematurely terminating in a terminal flower (Table S1, Figure 6R). Taken together, the results indicate that UFO-VP16 and SEP4-VP16 partly activate a similar developmental program and the dependence on LFY and SEP proteins suggest that these factors may co-regulate transcription of an overlapping group of downstream target genes.
UFO functions as a co-activator in concert with LFY and SEP transcription factors
UFO encodes an F-box protein, which was shown to interact with the SCF E3 ubiquitin ligase subunits ASK1, CUL1 and subunits of the COP9 signalosome, suggesting a role in ubiquitination of proteins involved in flower development . Recently LFY was shown to physically interact with UFO at the AP3 promoter to facilitate a potential interaction between UFO and promoter elements, and further to designate LFY as an ubiquitination substrate of UFO , . Consistent with UFO being part of a transcriptional complex, our results show that nuclear localization of UFO is required for its activity and that the Engrailed and VP16 based transcriptional modulators can modify its function. Expression of UFO lacking the F-box domain results in a loss-of-function phenotype which supports the “activation by destruction” model suggested for LFY transcription factor . In this model, ubiquitination of LFY by UFO enhances its activity likely through increased recycling of LFY on the target genes' promoters, along with recruitment of the RNA polymerase II to the complex and initiation of transcription , , , . Interestingly, the VP16 transactivation domain was unable to function in the absence of the F-box domain suggesting that the VP16 transactivator was unable to override the lack of LFY ubiquitination by UFO.
Our results also show that in addition to LFY, SEP proteins were required for the observed strong UFO-VP16 leaf serration phenotypes implying that SEP proteins may also associate with the UFO-LFY transcriptional complex. Overexpression of SEP1 resulted in early transition of the apical meristem into a terminal flower similar to the phenotypes of plants overexpressing LFY or SEP3 , , whereas SEP4-VP16 plants showed some phenotypic similarities with plants expressing UFO-VP16 in the flowers. These results are consistent with the study that showed physical interaction between LFY and SEP3 proteins, and further support the model that the UFO, LFY and SEP proteins most likely interact in a transcriptional complex to regulate a common set of target genes involved in meristem specification and flower development .
Function of UFO outside the APETALA3 domain
UFO has been shown to bind the AP3 promoter in the presence of LFY to activate its expression in the stage 3 flower primordia , . In the ufo mutant compared to wild type, AP3 expression is restricted to a narrower domain in stage 4 and in later stages of flower primordia . When UFO is overexpressed, the vegetative leaves become serrated, suggesting that the leaf primordia are responsive to changes in UFO expression . Previous studies have shown that ufo mutants display delayed transition of the vegetative to inflorescence identity of the apical meristem. Moreover, some ufo flowers also lack organs in the 1st and 4th whorls that are established before AP3 expression, whereas other flowers are substituted by filamentous structures , . In the ufo-1 mutant, AP1 expression is reduced in stage 1 and 2 flowers  and consistent with this, our results show ectopic AP1 expression in UFO-VP16 leaves. Taken together, these phenotypes indicate that UFO in the presence of LFY is also responsible for the activation of genes other than AP3.
It was previously shown that UFO expression is initiated very early in the embryonic shoot meristem by SHOOTMERISTEMLESS (STM) and is maintained in the peripheral zone (PZ) of the vegetative shoot (SAM) and inflorescence (IM) meristems throughout development , ,  (Figure 7A). In the SAM, UFO expression overlaps with that of LFY in the domains of P0 and P1 stage leaf primordia, whose expression in turn is initiated by the auxin maximum through MONOPTEROS (MP), an ARF family member of the auxin signaling pathway , . LFY is expressed at very low levels in the first primary leaf primordia, but becomes increasingly stronger in the upper rosette and cauline leaf primordia . In the later stages of leaf primordia, UFO expression is not detected whereas LFY continues to be expressed ,  (Figure 7A). In the IM, UFO and LFY expression domains overlap in stage 0 floral primordia. UFO is reactivated in the centre of stage 2 flower meristems after the establishment of the first sepal whorl. When AGAMOUS expression is initiated in the centre during early stage 3, UFO RNA is restricted to a cup-shaped domain between the first and fourth whorls followed by expression at the base of petals during stage 4 while the third whorl is established  (Figure 7A). Taken together, UFO expression is not restricted to the AP3 domain in the floral meristem, but overlaps with LFY during the early developmental stages of all lateral meristems/primordia suggesting an ancestral role in their establishment and fate specification.
A. UFO (blue) is expressed in the peripheral zone of the shoot apical (SAM) and inflorescence (IM) meristems. UFO is later induced in the centre of stage 2 floral meristems and its expression domain is restricted to the second and third whorls during later stages , . LFY expression (shades of orange) is initiated in the P0 leaf primordium and progressively increases in the later stages; its expression becoming prominent when floral meristems are initiated. The UFO and LFY expression domains overlap in the lateral P0 and P1 leaf primordia in the SAM, in stage 0 floral primordia in the IM, and in the petal, stamen and carpel whorls upon establishment , . B. LFY activity is enhanced by UFO in the emerging lateral meristems/primordia within the peripheral zones of the meristems to ensure their establishment and fating. Lower LFY activity without UFO promotes the organogenesis of the primordia during later stages.
UFO is involved in the establishment of meristems
Based on the native expression patterns of UFO and LFY, we propose two functional stages for LFY activity (Figure 7B). The earlier stage which involves UFO as a co-activator is important for the lateral meristem (primordia) establishment in the PZ of the SAM, whereas the later stage of LFY function, which does not involve UFO, is primarily to promote differentiation and organogenesis of the primordia. Over-expression of UFO or UFO-VP16 resulted in repeated lobing of the leaf primordia and delayed emergence in Arabidopsis (Figure 2G, H). In B. napus, the meristematic activity was continued in the margins of mature leaves expressing UFO-VP16, resulting in the production of continuous lobing and compound leaf forms (Figure 4). These results suggest that expanding the UFO expression into later stage leaf primordia prolongs the early stage function of LFY to allow continued meristem proliferation leading to serration and lobing of the leaf margins. It is interesting to note that ufo and lfy mutations do not affect the shape of the simple leaves in Arabidopsis, whereas in species with compound leaf forms, mutations in the orthologs result in a reduction of the compounded nature , , . In the ufo mutants, LFY by itself is not sufficient to establish lateral meristems as evidenced by the reduction or lack of floral organs and the flowers, and the presence of filamentous structures , . Additionally, the maintenance of the apical meristem is impaired, which is evident from the premature termination of the inflorescence meristem into a flower in strong ufo mutants. The milder ufo mutant phenotypes compared to those of lfy support the argument that UFO is not required for LFY functions in the later stages. Overexpression of LFY does not result in the production of serrated leaves with ectopic meristems, indicating that unlike UFO, increased LFY levels alone are not sufficient to extend the meristematic phase of the leaf primordia . However, seedlings overexpressing the hyperactive LFY-VP16 form of LFY in combination with UFO lead to growth arrest, implying that higher LFY activity is important for lateral meristem establishment and that a regulated lower activity is necessary to promote growth and differentiation . Overexpression of the F-box genes most similar to UFO (LEAF CURLING RESPONSIVENESS [LCR; At1g27340], At1g76920, At4g33160) with or without VP16 did not result in the production of aberrant phenotypes (not shown), whereas LCR has been implicated in the expansion of the leaf margin , suggesting that UFO does not function in a redundant manner with other F-box proteins.
UFO ensures the proper fating of meristems
Phytomers are produced by the apical meristem and their fates in turn determine the identity of the vegetative, inflorescence and floral meristems . The identities of the apical and lateral meristems are determined by the combinatorial co-expression of specific MADS box proteins during development . LFY is responsible for activation of the MADS box genes that specify the floral meristem (AP1, CAL, FUL) and floral organ identities (AP1, AP3, PI, AG, SEP) . Overexpression of LFY results in precocious expression of these MADS box genes leading to early flowering by homeotic transformation of the lateral shoots into single flowers followed by the premature conversion of the primary shoot into a terminal flower . These overexpression LFY phenotypes are not UFO dependent. However, overexpression of UFO-VP16 in the presence of wild type LFY results in ectopic flowers and inflorescences in the upper rosette and cauline leaves (Figure 2, 3). The arrangement of older floral meristems along the main leaf margins (Figure 2K, L) and the emergence of the new meristems in acropetal succession along the margins of the secondary leaf serrations (2L–N) are reminiscent of the acropetal development of flowers on the primary inflorescence. Furthermore, the positions of the secondary and tertiary serrations of the upper rosette leaves are indicative of a bract-like fate (Figure 2M, N) which becomes obvious in later stages of these ectopic inflorescences (Figure 2C, D). The source of the shoot-like phenotype of the leaves may originate in the axillary meristem. In Arabidopsis, immediately after emergence of the leaf primordium, a cell niche is specified in its axis for future development of the axillary meristems . REGULATOR OF AXILLARY MERISTEMS (RAX1) functions to specify this axillary meristem niche and its expression is directly induced by LFY . The fasciation of the co-inflorescences with the cauline leaves observed in UFO-VP16 suggests that the extended meristematic phase of the leaf primordia delays the boundary formation between the axillary meristems and the leaf primordia thus allowing the co-inflorescence meristem program to expand from the axis into the leaf primordia.
Contrastingly in the ufo mutants, homeosis of the lateral meristems/primordia is the result of insufficient induction of AP3 and AP1 , , but may also apply to other genes induced by LFY . In these situations, the primordia acquire an identity which was established earlier during development. For example in ufo flowers, petals become sepaloid and stamens carpelloid, whereas flowers are replaced by co-inflorescences or subtended by bracts. Taken together the UFO overexpression and ufo mutant phenotypes suggest that UFO in combination with LFY provides a framework for the meristems and organ primordia to establish the expression of the proper combination of identity genes, possibly by promoting the meristem fate and/or by suppressing downstream morphogenesis programs (Figure 7B).
UFO functions in other plant species
In Arabidopsis, flowers are produced in the lateral positions of the inflorescence meristem (raceme), whereas in tobacco, flowers are positioned at the terminus of the primary and co-inflorescences (cyme), which is a function of LFY and TERMINAL FLOWER1 (TFL1) expression in the IM . Thus the flower identity in a racemose inflorescence is specified de novo in the lateral meristems, whereas in a cyme, the flowers are produced by a transition of the (co-) inflorescence fate into a floral identity. In tobacco, overexpression of UFO and UFO-VP16 result in early flowering due to the precocious and gradual transition of the apical vegetative meristem into a terminal flower. Consistent with this interpretation, mutants of UFO orthologs DOUBLE TOP (DOT) and ANANTHA (AN) in the related Solanaceae species petunia and tomato, respectively, are unable to transit into a flower and instead reiterate the inflorescence program. The LFY orthologs NFL1 (tobacco), ABERRANT LEAF AND FLOWER (ALF petunia) and FALSIFLORA (FA tomato) are expressed like LFY in the lateral meristems produced by the vegetative and inflorescence meristems, but the NFL1 transcript levels are higher than those of LFY during the vegetative stage , , . The UFO orthologs DOT in petunia and AN in tomato are not expressed in the vegetative meristems, but are first activated in the IMs upon transition to flowering , . Thus in the cyme inflorescence, DOT/AN most likely plays an essential role to establish the floral identity in the apical meristem by activating the LFY orthologs.
The serrated leaves in UFO overexpressing Arabidopsis plants display some common features with UFO/LFY othologs in compound leaf development in other plant species. In the compound leaves of tomato the number of leaflets is slightly reduced in the fa mutant , although the majority of the leaf form is controlled by the KNOX gene pathway . However, the pea STP/UNI pathway is important for the initiation of pinnae (i.e. leaflet and tendril) primordia in the compound leaves. stp (UFO ortholog) mutants have reduced numbers of pinnae and uni (LFY ortholog) plants have trifoliate or simple leaves . Both of these mutants exhibit a prolonged meristematic phase while initiating lateral primordia in an acropetal manner and the process is reiterated in the lateral primordia upon ectopic expression of the LFY/UNI and/or UFO/STP genes . Both STP and UNI are expressed in early leaf primordia and UNI retains expression in the distal region of the marginal blastozone until the apex terminates in a distal tendril. In the afila and cochleata mutants UNI is also expressed in the pinnae and stipule primordia respectively, and results in the development of secondary rachis formation in these positions demonstrating that UNI promotes the rachis identity of the leaf . These observations raise an interesting possibility that the underpinning genetic network which increases compounding of the pea leaf by derepressing UNI, is similar to the reduced determinacy of the Arabidopsis leaves upon activation of LFY by overexpressing UFO. Moreover, the rachis specification of the leaf primordia by UNI and STP seems to operate in a similar fashion as the specification of the floral meristems in the inflorescence by LFY and UFO in Arabidopsis. More studies are required to address how LFY and UFO in combination with other genetic factors could produce different developmental outcomes in diverse plant species. In conclusion, we propose that the UFO orthologs play an ancestral role in activating LFY orthologs in the peripheral zone of the apical and floral meristems to promote the establishment and identity of the lateral meristems and primordia.
Materials and Methods
A new multiple cloning site including a C-terminal E-tag (GTTTAAACCAACTAGTAAAGATCTACAAGTTTGTACAAAGTGGTTCCGGGTGCGCCGGTGCCGTATCCGGATCCGCTGGAACCGCGTGCTCGAGCATCGCGAGCTCTAGA) was generated by overlapping primers and cloned in the PmeI and XbaI sites of the binary Gateway destination vector pK7WG2 (VIB-Ghent University). The t35S terminator was PCR amplified with primers CACCTCGCGATGACGGCCATGCTAGAGTCCGCA and TCTAGAGTCACTGGATTTTGGTTTTAGG, and cloned as an NruI/XbaI fragment in the respective sites of the new MCS. The BsrGI Gateway cassette (GW) fragment and the PmeI/SpeI p35S promoter fragment were reintroduced from pK7WG2 by cloning in the respective sites of the new MCS resulting in pER310. The engrailed repressor domain was PCR amplified from pLD16125 (Drosophila Genomics Resource Centre) with primers CACCACTAGTATGGCCCTGGAGGATCGCTG and AGATCTGGATCCCAGAGCAGATTTCTC and inserted at the N-terminal side of the GW site in pER310 resulting in pER311. The glucocorticoid receptor was amplified with primers CACCCTCGAGCAAAGAAAAAAATCAAAGGGATTC and TCGCGATCATTTTTGATGAAACAGAAG and cloned in frame downstream from the E-tag in pER310 leading to pER312. Likewise in pER430 the VP16 domain was inserted after amplification with primers CACCGCTCGAGCCCCCCCGACCGATGTCAGCCTG and TCGCGATCACCCACCGTACTCGTCAAT. YFP was amplified with primers CACCACTAGTCGACTTATGGTGAGCAAGGGCGAGGA and TCGCGATTAGGATCCCTTATACAGCTCGTCCATGCC and cloned C-terminal of the E-tag in pER310 resulting in pER562. The coding sequences without stop codon of UFO, UFOdelF (codons 50–62 deleted), SEP1, SEP4, and GUS were cloned in pDONR201 (Invitrogen) before recombination in the designated T-DNA destination vectors. The three-way pER557 was created by substituting the p35S promoter and attR1 fragment of pER310 with the attR4 recombination site. The promoters including the start codon of the Arabidopsis genes LFY (-2321), AP1 (-1455), AP3 (-1240), PI (-960) and AG (-563-codon 83) were cloned into pDONR P4-P1R (invitrogen) and combined with GUS or other genes in pER557 using LR clonase.
Plant materials, transformation and genotyping
Mutants used in this study: sgs2-1 , sep1,2,3,4 , lfy-1, ufo-1, ask1-1, ap1-10, pi-1, ap3-1 and ag were provided by the Arabidopsis Biological Resource Center (ABRC, Ohio). Plants were grown at 22°C, 4000 lux under long day (16 h light) or short day (10 h light) regimes. Constructs were transformed in wild type Arabidopsis thaliana ecotype Columbia or in mutants with their designated background using the Agrobacterium floral dip method . Transgenic plants were selected on ½ MS medium supplemented with 10 g/L sucrose and 10 mg/L L-PPT or 50 mg/L kanamycin, and transplanted in soil after seven days. UFO-GR plants were induced by spraying with 30 µM dexamethasone, 0.01% Tween-20 in water. Genotyping of the SEP alleles was performed as described by Ditta et al. . Brassica napus DH1250 hypocotyls and Nicotiana tabacum Xanthi leaf segments were used for Agrobacterium mediated transformation. The number of transgenic lines analyzed in this study is summarized in Table S1. Flowering time of the transgenic tobacco lines was compared with wild type after seeding T1 seed in soil and after selection for the transgene by spraying with 100 mg/L L-PPT + 50 µl/L Silwet.
The UFO, LFY, SEP1, 2, and 3 transcript levels and relative expression levels were quantified by qRT-PCR using actin 2 as internal controls using the methods described in . The qRT-PCR experiment was performed in triplicate on 5 pools of 10 day-old T1 seedlings of 35S:UFO-VP16 and Col WT using the Applied Biosystem Step One real-time PCR system and the SYBR Green PCR master mix as detailed in . The tissue used for qRT-PCR included the SAM and surrounding primary leaves. The primers used for qRT-PCR are listed in Table S2.
GUS staining and microscopy
Plant tissue was vacuum infiltrated in a solution containing 100 mM NaHPO4 pH 7.0, 10 mM Na-EDTA, 5 mM Na-ferricyanide, 5 mM K-ferrocyanide, 0.1% Triton X-100, 1 mg/ml 5-bromo-4 chloro 3 indolyl β-D-glucuronide (X-GlcU) and incubated overnight at 37°C. Tissue was cleared in 95% ethanol. Plant samples for scanning electron microscopy (SEM) were fixed overnight in 3% glutaraldehyde in 25 mM NaHPO4 buffer pH 7.0 at 4°C. After rinsing with the same phosphate buffer, samples were transferred to PO4 buffer with 1% OsO4 and incubated for 2 hours at room temperature. After rinsing with buffer the samples were transferred to 100% acetone with 10% increments. After two more changes with acetone the samples were critical point dried, mounted on aluminum stubs and coated with gold for 3 minutes in an Edwards S150B sputter coater. The samples were observed under a Phillips 505 scanning electron microscope at 30 kV and images were captured on Polaroid film. Images were scanned and edited in Adobe Photoshop CS (Adobe Systems, San Jose, California) to improve the contrast and place scale bars.
RT-PCR results of gene expression levels in p35S:UFO-VP16 seedlings compared to wild type Arabidopsis.
Summary of UFO transgenic lines used in this study showing the distribution of the various phenotypes.
Primers used for RT-PCR analysis.
We thank Shelley Hepworth and the two anonymous reviewers for their critical suggestions and helpful comments. National Research Council publication number 50141.
Conceived and designed the experiments: ER PV RD. Performed the experiments: ER PV DX VB. Analyzed the data: ER PV RD. Contributed reagents/materials/analysis tools: WC KK TD. Wrote the paper: ER PV RD.
- 1. Chandler JW (2012) Floral meristem initiation and emergence in plants. Cell Mol Life Sci 69: 3807–3818. doi: 10.1007/s00018-012-0999-0
- 2. Barton MK (2010) Twenty years on: The inner workings of the shoot apical meristem, a developmental dynamo. Dev Biol 341: 95–113. doi: 10.1016/j.ydbio.2009.11.029
- 3. Efroni I, Eshed Y, Lifschitz E (2010) Morphogenesis of Simple and Compound Leaves: A Critical Review. Plant Cell 22: 1019–1032. doi: 10.1105/tpc.109.073601
- 4. Wu S, Smith HS (2012) Out of step: The function of TALE homeodomain transcription factors that regulate shoot meristem maintenance and meristem identity. Frontiers in Biology 7: 144–154. doi: 10.1007/s11515-011-1182-y
- 5. Maizel A, Busch MA, Tanahashi T, Perkovic J, Kato M, et al. (2005) The floral regulator LEAFY evolves by substitutions in the DNA binding domain. Science 308: 260–263. doi: 10.1126/science.1108229
- 6. Huala E, Sussex IM (1992) LEAFY Interacts with Floral Homeotic Genes to Regulate Arabidopsis Floral Development. Plant Cell 4: 901–913. doi: 10.2307/3869458
- 7. Weigel D, Alvarez J, Smyth DR, Yanofsky MF, Meyerowitz EM (1992) LEAFY controls floral meristem identity in Arabidopsis. Cell 69: 843–859. doi: 10.1016/0092-8674(92)90295-n
- 8. Lee I, Wolfe DS, Nilsson O, Weigel D (1997) A LEAFY co-regulator encoded by UNUSUAL FLORAL ORGANS. Curr Biol 7: 95–104. doi: 10.1016/s0960-9822(06)00053-4
- 9. Parcy F, Nilsson O, Busch MA, Lee I, Weigel D (1998) A genetic framework for floral patterning. Nature 395: 561–566. doi: 10.1038/26903
- 10. Chae E, Tan QK, Hill TA, Irish VF (2008) An Arabidopsis F-box protein acts as a transcriptional co-factor to regulate floral development. Development 135: 1235–1245. doi: 10.1242/dev.015842
- 11. Levin JZ, Meyerowitz EM (1995) UFO: An Arabidopsis Gene Involved in Both Floral Meristem and Floral Organ Development. Plant Cell 7: 529–548. doi: 10.1105/tpc.7.5.529
- 12. Wilkinson MD, Haughn GW (1995) UNUSUAL FLORAL ORGANS Controls Meristem Identity and Organ Primordia Fate in Arabidopsis. Plant Cell 7: 1485–1499. doi: 10.2307/3870137
- 13. McKim S, Hay A (2010) Patterning and evolution of floral structures - marking time. Curr Opin Genet Dev 20: 448–453. doi: 10.1016/j.gde.2010.04.007
- 14. Moyroud E, Kusters E, Monniaux M, Koes R, Parcy F (2010) LEAFY blossoms. Trends Plant Sci 15: 346–352. doi: 10.1016/j.tplants.2010.03.007
- 15. Souer E, Rebocho AB, Bliek M, Kusters E, de Bruin RA, et al. (2008) Patterning of inflorescences and flowers by the F-Box protein DOUBLE TOP and the LEAFY homolog ABERRANT LEAF AND FLOWER of petunia. Plant Cell 20: 2033–2048. doi: 10.1105/tpc.108.060871
- 16. Gourlay CW, Hofer JM, Ellis TH (2000) Pea compound leaf architecture is regulated by interactions among the genes UNIFOLIATA, cochleata, afila, and tendril-lessn. Plant Cell 12: 1279–1294. doi: 10.2307/3871129
- 17. Samach A, Klenz JE, Kohalmi SE, Risseeuw E, Haughn GW, et al. (1999) The UNUSUAL FLORAL ORGANS gene of Arabidopsis thaliana is an F-box protein required for normal patterning and growth in the floral meristem. Plant J 20: 433–445. doi: 10.1046/j.1365-313x.1999.00617.x
- 18. Risseeuw EP, Daskalchuk TE, Banks TW, Liu E, Cotelesage J, et al. (2003) Protein interaction analysis of SCF ubiquitin E3 ligase subunits from Arabidopsis. Plant J 34: 753–767. doi: 10.1046/j.1365-313x.2003.01768.x
- 19. Lechner E, Achard P, Vansiri A, Potuschak T, Genschik P (2006) F-box proteins everywhere. Curr Opin Plant Biol 9: 631–638. doi: 10.1016/j.pbi.2006.09.003
- 20. Wang X, Feng S, Nakayama N, Crosby WL, Irish V, et al. (2003) The COP9 signalosome interacts with SCF UFO and participates in Arabidopsis flower development. Plant Cell 15: 1071–1082. doi: 10.1105/tpc.009936
- 21. Salghetti SE, Caudy AA, Chenoweth JG, Tansey WP (2001) Regulation of transcriptional activation domain function by ubiquitin. Science 293: 1651–1653. doi: 10.1126/science.1062079
- 22. Kim SY, Herbst A, Tworkowski KA, Salghetti SE, Tansey WP (2003) Skp2 regulates Myc protein stability and activity. Mol Cell 11: 1177–1188. doi: 10.1016/s1097-2765(03)00173-4
- 23. Lipford JR, Smith GT, Chi Y, Deshaies RJ (2005) A putative stimulatory role for activator turnover in gene expression. Nature 438: 113–116. doi: 10.1038/nature04098
- 24. von der Lehr N, Johansson S, Wu S, Bahram F, Castell A, et al. (2003) The F-Box Protein Skp2 Participates in c-Myc Proteosomal Degradation and Acts as a Cofactor for c-Myc-Regulated Transcription. Mol Cell 11: 1189–1200. doi: 10.1016/s1097-2765(03)00193-x
- 25. Mourrain P, Beclin C, Elmayan T, Feuerbach F, Godon C, et al. (2000) Arabidopsis SGS2 and SGS3 genes are required for posttranscriptional gene silencing and natural virus resistance. Cell 101: 533–542. doi: 10.1016/s0092-8674(00)80863-6
- 26. Zhao D, Yu Q, Chen M, Ma H (2001) The ASK1 gene regulates B function gene expression in cooperation with UFO and LEAFY in Arabidopsis. Development 128: 2735–2746.
- 27. Smyth DR, Bowman JL, Meyerowitz EM (1990) Early flower development in Arabidopsis. Plant Cell 2: 755–767. doi: 10.2307/3869174
- 28. Honma T, Goto K (2001) Complexes of MADS-box proteins are sufficient to convert leaves into floral organs. Nature 409: 525–529. doi: 10.1038/35054083
- 29. Smaczniak C, Immink RGH, Muiño JM, Blanvillain R, Busscher M, et al.. (2012) Characterization of MADS-domain transcription factor complexes in Arabidopsis flower development. Proc Natl Acad Sci U S A.
- 30. Weigel D, Nilsson O (1995) A developmental switch sufficient for flower initiation in diverse plants. Nature 377: 495–500. doi: 10.1038/377495a0
- 31. Castillejo C, Romera-Branchat M, Pelaz S (2005) A new role of the Arabidopsis SEPALLATA3 gene revealed by its constitutive expression. Plant J 43: 586–596. doi: 10.1111/j.1365-313x.2005.02476.x
- 32. Hepworth SR, Klenz JE, Haughn GW (2006) UFO in the Arabidopsis inflorescence apex is required for floral-meristem identity and bract suppression. Planta 223: 769–778. doi: 10.1007/s00425-005-0138-3
- 33. Long JA, Barton MK (1998) The development of apical embryonic pattern in Arabidopsis. Development 125: 3027–3035.
- 34. Reddy GV (2008) Live-imaging stem-cell homeostasis in the Arabidopsis shoot apex. Curr Opin Plant Biol 11: 88–93. doi: 10.1016/j.pbi.2007.10.012
- 35. Yamaguchi N, Wu M-F, Winter Cara M, Berns Markus C, Nole-Wilson S, et al. (2013) A Molecular Framework for Auxin-Mediated Initiation of Flower Primordia. Dev Cell 24: 271–282. doi: 10.1016/j.devcel.2012.12.017
- 36. Blazquez MA, Soowal LN, Lee I, Weigel D (1997) LEAFY expression and flower initiation in Arabidopsis. Development 124: 3835–3844.
- 37. Hofer J, Turner L, Moreau C, Ambrose M, Isaac P, et al. (2009) Tendril-less regulates tendril formation in pea leaves. Plant Cell 21: 420–428. doi: 10.1105/tpc.108.064071
- 38. Taylor S, Hofer J, Murfet I (2001) Stamina pistilloida, the Pea Ortholog of Fim and UFO, Is Required for Normal Development of Flowers, Inflorescences, and Leaves. Plant Cell 13: 31–46. doi: 10.2307/3871151
- 39. Molinero-Rosales N, Jamilena M, Zurita S, Gómez P, Capel J, et al. (1999) FALSIFLORA, the tomato orthologue of FLORICAULA and LEAFY, controls flowering time and floral meristem identity. Plant J 20: 685–693. doi: 10.1046/j.1365-313x.1999.00641.x
- 40. Song JB, Huang SQ, Dalmay T, Yang ZM (2012) Regulation of Leaf Morphology by MicroRNA394 and its Target LEAF CURLING RESPONSIVENESS. Plant Cell Physiol 53: 1283–1294. doi: 10.1093/pcp/pcs080
- 41. Smaczniak C, Immink RGH, Angenent GC, Kaufmann K (2012) Developmental and evolutionary diversity of plant MADS-domain factors: insights from recent studies. Development 139: 3081–3098. doi: 10.1242/dev.074674
- 42. Kaufmann K, Pajoro A, Angenent GC (2010) Regulation of transcription in plants: mechanisms controlling developmental switches. Nat Rev Genet 11: 830–842. doi: 10.1038/nrg2885
- 43. Keller T, Abbott J, Moritz T, Doerner P (2006) Arabidopsis REGULATOR OF AXILLARY MERISTEMS1 Controls a Leaf Axil Stem Cell Niche and Modulates Vegetative Development. Plant Cell 18: 598–611. doi: 10.1105/tpc.105.038588
- 44. Chahtane H, Vachon G, Le Masson M, Thévenon E, Périgon S, et al. (2013) A variant of LEAFY reveals its capacity to stimulate meristem development by inducing RAX1. Plant J 74: 678–689. doi: 10.1111/tpj.12156
- 45. Siriwardana NS, Lamb RS (2012) The poetry of reproduction: the role of LEAFY in Arabidopsis thaliana flower formation. Int J Dev Biol 56: 207–221. doi: 10.1387/ijdb.113450ns
- 46. Prusinkiewicz P, Erasmus Y, Lane B, Harder LD, Coen E (2007) Evolution and development of inflorescence architectures. Science 316: 1452–1456. doi: 10.1126/science.1140429
- 47. Kelly AJ, Bonnlander MB, Meeks-Wagner DR (1995) NFL, the tobacco homolog of FLORICAULA and LEAFY, is transcriptionally expressed in both vegetative and floral meristems. Plant Cell 7: 225–234. doi: 10.2307/3869998
- 48. Souer E, van der Krol A, Kloos D, Spelt C, Bliek M, et al. (1998) Genetic control of branching pattern and floral identity during Petunia inflorescence development. Development 125: 733–742.
- 49. Lippman ZB, Cohen O, Alvarez JP, Abu-Abied M, Pekker I, et al. (2008) The making of a compound inflorescence in tomato and related nightshades. PLoS Biol 6: e288. doi: 10.1371/journal.pbio.0060288
- 50. Bharathan G, Goliber TE, Moore C, Kessler S, Pham T, et al. (2002) Homologies in leaf form inferred from KNOXI gene expression during development. Science 296: 1858–1860. doi: 10.1126/science.1070343
- 51. Ditta G, Pinyopich A, Robles P, Pelaz S, Yanofsky MF (2004) The SEP4 gene of Arabidopsis thaliana functions in floral organ and meristem identity. Curr Biol 14: 1935–1940. doi: 10.1016/j.cub.2004.10.028
- 52. Clough SJ, Bent AF (1998) Floral dip: a simplified method forAgrobacterium-mediated transformation ofArabidopsis thaliana. Plant J 16: 735–743. doi: 10.1046/j.1365-313x.1998.00343.x
- 53. Xiang D, Yang H, Venglat P, Cao Y, Wen R, et al. (2011) POPCORN functions in the auxin pathway to regulate embryonic body plan and meristem organization in Arabidopsis. Plant Cell 23: 4348–4367. doi: 10.1105/tpc.111.091777