In fungi and metazoans, the SCF-type Ubiquitin protein ligases (E3s) play a critical role in cell cycle regulation by degrading negative regulators, such as cell cycle-dependent kinase inhibitors (CKIs) at the G1-to-S-phase checkpoint. Here we report that FBL17, an Arabidopsis thaliana F-box protein, is involved in cell cycle regulation during male gametogenesis. FBL17 expression is strongly enhanced in plants co-expressing E2Fa and DPa, transcription factors that promote S-phase entry. FBL17 loss-of-function mutants fail to undergo pollen mitosis II, which generates the two sperm cells in mature A. thaliana pollen. Nonetheless, the single sperm cell-like cell in fbl17 mutants is functional but will exclusively fertilize the egg cell of the female gametophyte, giving rise to an embryo that will later abort, most likely due to the lack of functional endosperm. Seed abortion can, however, be overcome by mutations in FIE, a component of the Polycomb group complex, overall resembling loss-of-function mutations in the A. thaliana cyclin-dependent kinase CDKA;1. Finally we identified ASK11, as an SKP1-like partner protein of FBL17 and discuss a possible mechanism how SCFFBL17 may regulate cell division during male gametogenesis.
Citation: Gusti A, Baumberger N, Nowack M, Pusch S, Eisler H, Potuschak T, et al. (2009) The Arabidopsis thaliana F-Box Protein FBL17 Is Essential for Progression through the Second Mitosis during Pollen Development. PLoS ONE 4(3): e4780. https://doi.org/10.1371/journal.pone.0004780
Editor: Markus Grebe, Umeå Plant Science Centre, Sweden
Received: December 18, 2008; Accepted: January 22, 2009; Published: March 11, 2009
Copyright: © 2009 Gusti 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: Funding was provided by the CNRS to P.G and A.S., the EU NoE (Rubicon LSHG-CT-2005-018683) to P.G. and the VW foundation to A.S. 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.
Regulation of protein stability through the ubiquitin proteasome system (UPS) is a major mechanism underlying many different cellular and organismal processes, such as cell division, DNA repair, quality control of newly produced proteins, regulation of developmental pathways, important parts of immune defence and in plants, light and phytohormone signal transduction –. Degradation via the UPS is a two-step process: the target protein is first tagged by covalent attachment of ubiquitin and subsequently degraded by a multicatalytic protease complex called the 26S proteasome. Conjugation of ubiquitin to the protein involves a cascade of three enzymes: E1, E2 and E3. Ubiquitin-activating enzyme (E1) forms a high-energy thioester intermediate, E1-S∼Ubi, which is then trans-esterified to one of the several ubiquitin conjugating enzymes (E2s). The transfer of ubiquitin from the E2-S∼Ubi to an ε-NH2 group of an internal lysine residue in the target protein, requires an ubiquitin protein-ligase (E3). Because E3 enzymes determine the substrate specificity, they are recognized to play the most important role in the ubiquitylation reaction.
Among the different classes of E3s, two of them, the SCF and the Anaphase Promoting Complex/Cyclosome (APC/C), dominate cell cycle regulation, such as DNA replication and cell division, respectively. Whereas the APC/C permits progression and exit from mitosis by inducing proteolysis of different cell cycle regulators including PDS1/SECURIN and CYCLIN B (reviewed in ), the budding yeast SCFCDC4 and the mammalian SCFSKP2 (the name of the F-box protein being indicated in uppercase) are required to destroy the cell cycle-dependent kinase inhibitors (CKIs) SIC1 and p27Kip1, respectively (reviewed in , ) and thus promote the entry into S-phase. It is noteworthy that the human SCFSKP2 E3 targets other essential regulators of S-phase progression, including cyclin E , E2F1 , the RB-like p130 protein  and the licensing factor for DNA replication CDT1 .
In plants, the role of the APC/C as a mitotic regulator has been established (discussed in ), however the proteolytic machinery at the G1/S-phase transition is still poorly characterized. Nevertheless, in the model plant A. thaliana, loss-of-function mutants in CULLIN1 arrest embryogenesis very early at the zygote stage , which is consistent with a role of an SCF E3 in cell cycle control. Moreover, two F-box proteins, similar to the metazoan SKP2, called SKP2A and SKP2B, have been identified in A. thaliana –. SCFSKP2A recruits cyclin-dependent kinase (CDK)-phosphorylated E2Fc, a negative regulator of cell division and its partner DPb, for proteolysis , . In addition, plant genomes encode also proteins sharing a short amino acid motif with the mammalian KIP/CIP-type CKIs –. A. thaliana counts seven such proteins called ICK1/KRP1, ICK2/KRP2, KRP3, KRP4, KRP5, KRP6 and KRP7. Despite poor homology conservation with the metazoan CIP/KIP proteins, plant ICK/KRPs bind to and inhibit several CDK complexes (likely A-type CDK associated to A- or D-type cyclins) (reviewed in ). At least two A. thaliana ICK/KRPs, ICK1/KRP1 and ICK2/KRP2, are degraded by the 26S proteasome , . SCFSKP2B may participate in the degradation of A. thaliana ICK/KRPs, because overexpression of the F-box protein SKP2B decreases the accumulation of ectopically expressed ICK/KRP1 and suppressed the ICK1/KRP1-dependent serrated leaf phenotype . However, skp2a skp2b double mutant plants develop normally and do not stabilize ICK1/KRP1 , indicating a residual but sufficient activity of SCFSKP2 in this skp2 mutant background and/or multiple E3s targeting redundantly ICK/KRPs.
Here, we characterized a novel F-box protein from A. thaliana called FBL17 that is involved in cell cycle regulation during pollen development. Reproduction in angiosperms relies on the production of two types of spores, microspores and megaspores, that give rise to male and female gametophytes, respectively , . After meiosis, each microspore is first subjected to an asymmetric cell division (pollen mitosis I, PMI) producing the vegetative cell and a generative cell. Whereas cell division is arrested in the vegetative cell, the generative cell undergoes a second cell division (pollen mitosis II, PMII) leading to two sperm cells.
Loss-of function of FBL17 impairs PMII resulting in bicellular pollen. The single sperm cell, however, can fertilize the egg cell of the female gametophyte, giving rise to an embryo that will abort, most likely by lack of functional endosperm. This phenotype is similar to the loss-of-function of the central cell cycle regulator cyclin-dependent kinase A;1 (CDKA;1) , . A model explaining how SCFFBL17 could regulate PMII will be discussed.
FBL17 is an essential gene in Arabidopsis
To better characterize the role of the SCF in plant cell cycle function, we searched for F-box protein encoding genes that are expressed in a cell cycle dependent manner. Among the ∼700 A. thaliana F-box proteins , one of them, called FBL17 (At3g54650) was of particular interest because its expression was found to be 2.5 fold increased in S-phase based on available microarray data . Moreover, this gene was in silico identified as a putative target of E2F transcription factors . A. thaliana plants co-expressing ectopically E2Fa with its dimerization partner, DPa, display strongly induced cell proliferation rates  and indeed in these plants, we found a 15-fold increase in FBL17 transcript accumulation (Figure 1A).
(A) FBL17 transcript accumulation in plants over-expressing the E2Fa transcription factor and its dimerization partner, DPa. Quantitative RT-PCR on RNA extracted from E2Fa-DPa overexpressing (OE) seedlings show a 15-fold increase in the relative abundance of FBL17 transcript compared to control RNA (Col-0). The experiment was three times repeated. Data are means±SE. (B) Diagram of the genomic locus of FBL17. The two T-DNA insertions disrupt the 7th exon and the 6th intron in the fbl17-1 and fbl17-2 allele respectively. Light grey filling indicate non-translated region of the transcript whereas dark grey filling indicates coding sequence. (C) Wild type silique opened to reveal the seed content. (D) Heterozygous fbl17-1+/− silique displaying a reduced fertility and aborted seeds (marked by white arrows). (E) Homozygous fbl17-1 mutant complemented with the FBL17 genomic clone show wild type siliques and normal seed development. (C, D, E, bar = 500 µm).
FBL17 is an LRR-type F-box protein, which has no close paralog in Arabidopsis. To gain insights into the function of FBL17, we isolated two A. thaliana T-DNA insertion mutants, named fbl17-1 and fbl17-2, in which the T-DNA insertions interrupt the 7th exon and 6th intron, respectively (Figure 1B). Ninety-six fbl17-1 and 102 fbl17-2 seedlings were genotyped and none of them was found homozygous for the mutation, suggesting that FBL17 is an essential gene in Arabidopsis. However, heterozygous fbl17-1 and fbl17-2 plants appeared normal in morphology during sporophytic development. As both lines contained single T-DNA insertions with integral sulphadiazine selection markers, we self-pollinated heterozygous mutant plants and analyzed the segregation of this marker in their progeny. This genetic analysis revealed a segregation ratio close to 1∶1 (53% of SulfR plants at most; Table 1), which is consistent with a gametophytic defect. Moreover, open siliques from self-pollinated fbl17-1 and fbl17-2 heterozygous plants showed a large proportion of aborted seeds (∼44%, see Table 2 and Figure 1C–E). Therefore we analyzed the T-DNA transmission of fbl17-1 and fbl17-2 by reciprocal crosses with wild type plants. A severe reduction in the transmission rate was only observed when heterozygous fbl17 mutants were used as a paternal partner (Table 1).
To demonstrate that this phenotype is caused by the fbl17-1 mutation, we engineered a rescue construct (pFBL17∶FBL17) consisting of 868-bp of the promoter sequence fused to FBL17 full length genomic sequence. Transgenic lines expressing this construction fully complemented the fbl17-1 seed abortion phenotype (Table 2, Figure 1C–E).
fbl17 mutants produce pollen with only a single sperm cell
A failure to transmit mutant alleles through the pollen can be caused by defects in pollen viability and/or development, germination, pollen tube growth or even fertilization. To test for pollen viability, we used Alexander's staining . Similarly to mature pollen grains from wild type plants, pollen from heterozygous fbl17-1 and fbl17-2 mutants appeared full, round and red-stained when treated with Alexander's stain (Figure 2A,B), showing that the mutation does not affect pollen viability.
fbl17 (A) and wild type (B) mature pollen viability test by coloration with Alexander's stain. The purple staining indicates that the grains are viable. Dehiscent pollen of qrt1-1−/− (C) and qrt1-1−/−, fbl17-1+/− (D) stained with DAPI and observed under UV fluorescence. The four pollen grains of the tetrad show two densely stained sperm cell nuclei and one large diffuse vegetative cell nuclei in qrt-1 mutants, whereas two pollen grains of the tetrad show only a single germ cell nuclei in qrt1-1,fbl17-1+/− double mutants. (E, F) transmitted light picture of C and D. (G–L) Expression of the HT10 gene in the fbl17 mutant pollen. Expression of the HTR10-mRFPprotein under the HTR10 promoter in fbl17-1 (H) and wild type (K) pollen, counterstained with DAPI (G, fbl17-1; J, wild type). (I, L) transmitted light pictures of G and J. (A, B) bar = 100 µm; (C–L) bar = 10 µm. (M–U) Promoter-GUS analysis of FBL17 expression in pollen. (M, P, S) DAPI staining is applied to reveal the developmental stage of the pollen grain. (N–U) X-Gluc histochemical staining of pFBL17∶GUS (N, Q, F) and non-transformed Col-0 (O, R, U) pollen grains. Bars = 10 µm (V) DNA content measurement of wild type germinative cell nuclei at prophase (n = 9; DNA = 2C), wild type sperm cell nuclei at telophase (n = 16), WT sperm cell nuclei at anthesis (n = 111) in comparison to the unique germ-cell like nuclei of fbl17 pollen (n = 77). Error bars = standard error mean.
Next, we investigated pollen development. In A. thaliana plants, after meiosis, wild type haploid microspores undergo a first mitotic division resulting in a vegetative cell and a generative cell, which divides a second time. Thus, wild type mature pollen contains one large vegetative cell and two sperm cells. Strikingly, about 45% of the heterozygous fbl17-1 and fbl17-2 mature mutant pollen exhibited only one generative-like cell (Table 3), indicating a failure to progress through the second mitotic division. To analyze this in more detail, we performed a tetrad analysis by crossing fbl17-1 to quartet mutation qrt1-1 , which causes the four products of male meiosis to remain attached (Figure 2C–F). Pollen produced by flb17-1+/−; qrt1-1−/− plants never contained more than two aberrant grains and rarely contained fewer, indicating that fbl17-1 is a highly penetrant male-gametophytic mutation.
To confirm that FBL17 is expressed in mature pollen as suggested by microarray data , we generated a GUS promoter-reporter with the FBL17 promoter sequence that we have above shown to be functional, and introduced it into wild type plants. Histochemical staining revealed that FBL17 expression is detectable during the microspore to bi-cellular pollen transition and fades later when pollen reaches the tricellular stage (Figure 2M–U).
To examine whether fbl17-1 mutation affects pollen cell fate, we introduced in the fbl17+/− background the H3.3 histone variant pHTR10-HTR10-mRFP marker, which is specifically expressed in the male germ line and accumulates in the nuclei of wild type generative cell and subsequently in sperm cells . Expression of this marker was observed in the generative-like cell nuclei of fbl17-1 mutant (n = 95), indicating that this cell has not lost its gametic fate (Figure 2G–L). Furthermore, the single generative-like cell nuclei of fbl17 mutant pollen is distinctively larger and less dense than the sperm cell nuclei observed in wild type pollen at anthesis (Figure 2D) and its morphology is reminiscent of the generative cell nuclei before the second mitotic division. Accordingly, measurement of DNA content by densitometry of DAPI stained pollen nuclei revealed that fbl17 single generative-like cell nuclei have a slightly higher content than the wild type sperm cell nuclei at anthesis (1,38C vs 1,25C respectively; Figure 2V). Thus, the fbl17 generative-like cell fails to progress into mitosis but has initiated S-phase reminiscent of wild-type sperms before fertilization. This suggested that the single generative-like cell of fbl17 mutant pollen might function as a sperm cell.
fbl17 single sperm cell predominantly fertilizes the egg cell in the embryo sac and causes seed abortion
Overall, our results indicate that fbl17 mutation prevents entry of the generative cell into mitosis, supporting a function of the FBL17 protein in cell cycle regulation in the male germ line. Interestingly, the production of a single sperm cell has recently been described for the loss of function of CDKA;1, the central A. thaliana cyclin-dependent kinase , . In these studies, it was found that the single sperm cell of cdka;1 may fertilize preferentially the egg cell in the embryo sac, leading to embryo arrest at the globular stage and fertilization-independent endosperm development.
To further investigate the functionality of the single generative-like cell and the origin of semi-sterility of fbl17 plants, we characterized the embryo sac development of plants fertilized with fbl17 pollen. Siliques of selfed fbl17-1 and fbl17-2 plants showed arrested embryos at the globular stage with underdeveloped endosperm (Figure 3). These embryos never developed further and eventually degenerated. When fbl17-1 pollen was used to fertilize wild type plants, the same phenotype was observed (Figure 3A, C, E, F). Hence, fbl17 mutants fully phenocopy the cdka;1 mutation.
Embryo development in wild type plants fertilized with fbl17-1 mutant (A, E) and wild type (B) pollen, 3 days after pollination. Embryo development in wild type plants fertilized with fbl17-1 mutant (C, F) and wild type (D) pollen, 4 days after pollination. Early fertilization-independent development of the endosperm is visible in fbl17-1-fertilized seeds (E) as evidenced by the presence of multiple nuclei (asterisks). Arrested globular embryo in fbl17-1 mutant seeds with degenerated endosperm (F). Bars: 50 µm.
fbl17 embryos are rescued by fis-class mutants
Malfunction of the FIS-Polycomb group complex leads to central cell proliferation even in the absence of fertilization (reviewed in –). A striking observation was that mutations of genes encoding this complex, including mea, fis2 and fie, could rescue the cdka;1 paternally conferred seed abortion phenotype and allowed the formation of viable seeds with only a diploid endosperm . To test whether flb17 fertilized ovules behave in a similar manner, we crossed female fie+/− mutant with pollen from the heterozygous fbl17-1 and fbl17-2 mutants. The F1 generation was then genotyped to assess the transmission of both the fbl17 and fie mutant alleles (Table 4). In contrast with Col-0 fertilized by fbl17 mutants that only allowed 6–8% of transmission efficiency of the fbl17 mutant allele, the fie mutation raised the transmission efficiency of fbl17 to 27–32%. At the same time, the transmission efficiency of the fie mutant allele through the female gametophyte increased from 8% in crosses with wild-type pollen to 28–32% indicating a mutual rescue of fbl17 and fie similar to what has been previously reported for fis mutants and cdka;1. Taken together, we conclude that the single fb17 generative-like cell is able to some degree to function as a sperm cell leading to the production of viable seed when sufficiently developed endosperm is provided.
FBL17 interacts with specific ASKs to form SCF-like complexes
Since FBL17 carries an F-box motif, we next examined whether this protein forms an SCF-type complex. Yeast two hybrid assays were conducted with the different A. thaliana SKP1-like proteins, called ASKs . In yeast, several ASKs were able to interact with FBL17 when fused to the GAL4 DNA binding domain while failing to allow yeast growth on selective medium when fused to the activating domain (Figure 4A). In contrast, ASK11 displayed a robust interaction with FBL17 in both fusions. Interestingly, ASK11 is among the members of the A. thaliana ASK family that are strongly expressed in pollen ,  and constitutes therefore a strong candidate for participating in an SCFFBL17 complex. It is noteworthy that the most predominant ASK, ASK1, was not found to interact with FBL17 in our yeast-two hybrid experiment. To further test a possible interaction between FBL17 and ASK11, we performed bimolecular fluorescence complementation (BiFC) experiments. As a control we fused to the N- and C-terminal half of YFP to the C-terminus of FBL17 and GUS, respectively. After co-injection of these fusion constructs into Nicotiana benthamiana leaf cells no YFP fluorescence could be found (data not shown). In contrast, when split-YFP fusions with FBL17 and ASK11 were co-injected, a strong fluorescence signal was recovered corroborating an interaction between these two components of an SCF-type complex in vivo (Figure 4B–G). Moreover transient expression of YFP fusions revealed that the FBL17 protein is essentially nuclear, whereas ASK11 localizes both to the cytoplasm and the nucleus (Figure 4B–E). Consequently, an interaction between ASK11 and FBL17 in the BiFC assays was restricted to nuclei (Figure 4F,G).
(A) Yeast-two-hybrid analysis of the interaction between FBL17 and ASKs. Yeast were grown for 3 days at 28°C. LTH- 3AT, low stringency selection, LTA, high stringency selection. Negative controls were done with empty bait vectors (pGBD) or empty prey vectors (pGAD). (B–G) Subcellular interaction of FBL17 with ASK11. Confocal laser-scanning micrographs of the abaxial surface of N. benthamiana leaves. (B, C) Transient expression of ASK11-YFP. The YFP signal is detected both in cytoplasm and nucleus. (D, E) Transient expression of FBL17-YFP. The signal is exclusively nuclear. (F–G) BiFC of FBL17-YN/ASK11-YC. Reconstitution of functional YFP as detected by YFP fluorescence occurs only in the nucleus. (H–K) Subcellular interaction of FBL17 with KRP7. (H, I) Transient expression of KRP7-YFP. A weak YFP signal in the cytoplasm and a strong signal in the nucleus can be detected. (J, K) BiFC of FBL17-YN/KRP7-YC. Reconstitution of functional YFP as detected by YFP fluorescence occurs only in the nucleus. (B, D, F, H, K, J) DIC images of the cells documented. (C, E, G, I, K) laser confocal micrograph of the YFP signal. Scale bars in B to K represent 45 µm.
FBL17 interacts with KRP7 in vivo
The FBL17 loss-of-function pollen phenotype is similar, if not identical, to the recently described cdka;1 mutant  strongly supporting a cell cycle function of this F-box protein. An interesting hypothesis is that an SCFFBL17 E3 ligase targets one or more members of the plant cell cycle-dependent kinase inhibitors, called ICK/KRPs (reviewed in , ). In such a scenario, ICK/KRPs would accumulate in fbl17 mutant pollen and consequently would inhibit the kinase activity mimicking the cdka;1 mutant phenotype. To test this possibility, we first carried out yeast two-hybrid experiments, with binding and activation domain fusions of both FBL17 and all seven KRPs being tested. However, no strong interaction between FBL17 and KRPs were observed (not shown). This lack of protein interaction was, however, not unexpected because most SCF substrates require post-translational modifications , which may not occur in yeast. To circumvent this problem we performed bimolecular fluorescence complementation (BiFC) experiments with three ICK/KRPs, KRP3, KRP5 and KRP7 that are expressed in pollen . We also used KRP1, which is not expressed in pollen, as a control. No signal could be recovered when split-YFP fusion constructs of KRP1, KRP3, or KRP5 were co-injected with FBL17 into Nicotiana benthamiana leaf cells (data not shown). In contrast, we observed a weak but distinct nuclear interaction when FBL17 and KRP7 were co-injected (Figure 4H–K).
KRP7 protein shows strong sequence similarity to KRP6, which was recently found to be expressed in pollen, as early as meiosis . Interestingly, KRP6 turnover is necessary for cell cycle progression during gametogenesis. Thus we ordered krp6 and krp7 mutants from the stock centers but only krp6 mutants could be obtained. In one T-DNA insertion mutant line, called krp6-1, KRP6 expression was abolished as indicated by qRT-PCR analysis (not shown). Homozygous krp6-1 mutant plants showed no visible mutant phenotype. Strikingly, the krp6-1+/− fbl17-1+/− double mutant, showed a partial rescue of fbl17 pollen phenotype in F1 with the ratio of aberrant pollen of ∼35%, a number significantly lower than the ∼48% observed in fbl17+/− mutant (Table 5). From these experiments, we conclude that KRP6 and most likely KRP7 are targets of an SCFFBL17 during pollen development.
FBL17 interacts with ASK11 and other ASKs
SCF-type complexes are involved in many developmental and physiological processes (reviewed in ). However so far, little is known about SCF complexes during gametophyte development. Here we investigated the function of FBL17, an F-box protein that is expressed during pollen development. Because FBL17 carries an N-terminal F-box domain, we first tested whether it associates with ASK proteins. The A. thaliana genome encodes 21 different ASKs . However, the great majority of functionally characterized A. thaliana F-box proteins were shown to associate with ASK1 and ASK2, which exhibit broad expression patterns throughout plant development. Interestingly, ASK1 and ASK2 function during male meiosis  and in cell cycle regulation as cell division during embryogenesis is affected in the double ask1 ask2 mutant . Here we provide evidence that FBL17 can interact with several ASKs. In particular we observed the strongest interaction with ASK11, which is also expressed in pollen ,  and known to interact with A. thaliana CUL1 . Although we cannot exclude that FBL17 participates in many CUL1-type E3 complexes, our data supports the existence of a novel type of SCF E3 ligase, formed by CUL1, ASK11 and FBL17 regulating male germ line development.
FBL17 is involved in cell cycle function during male gametogenesis
In fungi and metazoans, the SCF-types E3s play a critical role during the cell cycle at the G1-to-S-phase transition by degrading negative regulators such as CKIs. Whether such a mechanism is conserved in plants remained unclear. Consistently with this scenario, A. thaliana cul1 loss-of-function mutants arrest early during embryogenesis at the zygote stage  and also exhibit a reduced transmission of the mutation through both male and female gametophytes. However, such a phenotype was not reported for any of the ∼700 F-box encoding genes in A. thaliana.
Here, we provide evidence that FBL17 is a key regulator of the cell cycle during gametophyte development. First, FBL17 is expressed at the G1-to-S-phase transition  and its expression is strongly enhanced in plants ectopically co-expressing the S-phase transcription factor E2Fa together with its dimerization partner DPa. It is noteworthy that FBL17 promoter sequence carries the canonical E2F binding sites in both A. thaliana and rice . Whether FBL17 is a direct target of E2Fs, however, is not established yet.
Second, the FBL17 loss-of-function mutants arrest germ cell division leading to a single sperm cell phenotype that closely resembles (see also below) the phenotype found in mutants for the major cell cycle regulator; CDKA;1.
The paternal effect of fbl17 mutants leads to seed abortion, which is characterised by an arrest of embryo development at the globular stage and a defect in endosperm development. Similarly to the cdka;1 mutant , it is likely that the fbl17 single sperm cell may preferentially fertilize the egg cell, but not the central cell in the embryo sac. In both cases, the uniparental underdeveloped endosperm, which is unable to nourish the embryo, may thus be the cause of seed abortion. Hence, when the arrest of endosperm development is released by the mutation of FIE, a component of the Polycomb group complex, we observed at least a partial rescue of the paternally conferred fbl17 seed abortion phenotype.
FBL17 targets negative regulator(s) of the cell cycle
Based on the pollen phenotype, we propose that FBL17 targets a negative regulator of the cell cycle. Because fbl17 mutants phenocopy CDKA loss-of-function alleles, we speculated that the negative regulator targeted by FBL17 may directly act at the level of CDKA;1. Plausible candidate proteins are CKIs, whose accumulation during gametogenesis would lead to CDKA;1 inactivation and as a consequence cell cycle arrest. Indeed, we observed a physical interaction between FBL17 and at least one members of the KRP family (e.g., KRP7). Moreover, KRP6 mutation suppressed, at least partially, the fbl17 pollen phenotype. After the completion of this work Kim et al.  reported a similar role of FBL17 during male gametogenesis. This study showed that both KRP6 and KRP7 are expressed in the male germ cells after asymmetric division, but disappear in sperm cells. Based on their in vitro degradation assays and the fact that a KRP6-GFP fusion protein remained stable in the fbl17 single germ cell, these authors also proposed that KRP6 and KRP7 are the main target this SCF E3 ligase . Nevertheless, because a krp6 krp7 double loss-of-function mutant is not available, this model still awaits a definitive genetic prove.
An interesting question, which has not yet been fully answered, is at which stage the cell cycle fbl17 mutant arrests? Based on our knowledge of the cell cycle in yeast and animals, a naïve prediction was that fbl17 loss-of-function mutants would arrest at the G1/S transition. However, this was not the case because the mutant pollen had a higher DNA content than wild-type sperm and thus must have entered into S-phase ( and our work). In contrast, the DNA content of fbl17 was measured to be lower than 2C and thus, the mutant sperms appear to be not arrested at the entry into mitosis. However, as the fbl17 single germ cell fertilizes the egg cell, even allowing complete embryo development in a fie mutant background, we exclude that an aneuploid situation arose after fertilization and thus, it is likely that DNA replication was completed at the time of fertilization. Thus, we speculate that fbl17 mutants are arrested in the G1 phase and similarly to wild type would be still susceptible to an S-phase trigger late in development. This trigger would then be able to overwrite the FBL17 loss-of-function. It is noteworthy here that FBL17 expression is abolished in late pollen developmental stages as based on our promoter-reporter lines and . Alternatively, the loss of an SCFFBL17 complex might result in slow, but none the less steady progression into S-phase. This S-phase might then, similar to wild type, be only completed shortly before fertilization and thus, the generative-like-cells of fbl17 mutants would resemble wild-type sperm cells.
Multiple components of UPS regulate A. thaliana male gametogenesis
Recent work has shown that KRP6 is also targeted by two related RING-H2-type E3s, called RHF1a and RHF2a, during pollen development . Contrarily to fbl17, the rhf1a rhf2a double mutant pollen phenotype is partially penetrant and pollen development is arrested at multiple stages. Constitutive overexpression of KRP6 could phenocopy the rhf1a rhf2a double mutant defects. Thus, ICK/KRP degradation is regulated at different levels during pollen development (Figure 5). Although additional experiments are required to determine the exact contribution of each E3 in KRP6/7 turnover, RHF1a and RHF2a do not seem to act redundantly with SCFFBL17 to allow entry into PMII.
In this model RHF1a and RHF2a mediate KRP6 26S-proteasome-dependent degradation starting from meiosis . RHF1a and RHF2a loss-of-function of leads to KRP6 accumulation and as a consequence blocks both PMI and PMII. The SCFFBL17 E3, most likely containing ASK11, mediates KRP6/7 (and eventually other proteins) is strictly required to allow PMII to occur ( and our work). The role of UBP3 and UBP4 during pollen development remains to be determined.
With this, KRP turnover in plant cells, at least in the germ line, show similarities with the situation found in mammals where the cell cycle-dependent kinase inhibitor protein p27KIP1 is degraded by two different classes of E3s; the SCFSKP2 and the RING-type KPC1/KPC2 . The KPC E3 mediates polyubiquitinylation of p27KIP1 in the cytoplasm in a phosphorylation-independent manner during G1 phase, whereas SCFSKP2 is involved in phosphorylated-dependent p27KIP1 degradation in the nucleus during S and G2 phases . Whether SCFFBL17 recruits phosphorylated ICK/KRPs is unknown. Nevertheless, it has been shown that at least one A. thaliana ICK/KRP is subjected to proteolysis in a phosphorylation-dependent manner . In agreement, putative CDKA;1 phosphorylation sites are present in both KRP6 and KRP7 protein sequences .
Not only ubiquitylation, but also deubiquitylation has recently been involved in pollen development . Hence two closely related A. thaliana Ub-specific proteases (UBPs) called UBP3 and UBP4 are important for pollen mitosis II, as their combined disruption also leads to a single sperm cell, which however is unfertile. The target of UBP3/UBP4 is unknown. Interestingly, recent work in mammals identified USP19 as a UBP that regulates the protein level of KPC1, the catalytic subunit of KPC . In their model, USP19 stabilizes KPC1 and thus indirectly promotes degradation of p27KIP1 in the cytoplasm. Whether the plant UBP3/UBP4 have a similar effect on ICK/KRP accumulation during pollen development is worth to investigate.
Materials and Methods
Plant material and growth conditions
A. thaliana plants used in this study were all derived from the Columbia-0 (Col-0) accession. The lines qrt1-1 , fbl17-1 (GABI-170E02) fbl17-2 (GABI-436F11), krp6 (SAIL_548-B03) and fie (GABI_362D08) were obtained from the NASC stock centre. The position of the T-DNA inserts in the fbl17 lines were verified by DNA sequencing of the flanking regions amplified with primer pairs GABI T-DNA LP/7, GABI T-DNA RP/8 for fbl17-1 and GABI T-DNA LP/9, GABI T-DNA RP/10 for fbl17-2 (see oligo table below the GABI web site: http://www.gabi-kat.de). Those primer pairs were also used for genotyping. The transgenic lines E2Fa/DPa over-expressing line and pHTR10-HTR10-mRFP have been described elsewhere , . For most experiments, plants were grown on soil under standard greenhouse conditions (22°C, 16 h light photoperiod). Analysis of the fbl17 alleles transmission efficiency and selection of heterozygous fbl17 plants were performed by growing seedlings on sterile 1× Murashige and Skoog agar medium supplemented with 10 µg/ml sulfadiazine.
Constructs and transformation
The complementation genomic construct was generated by insertion of a 3747nt-long PCR amplified genomic product from (–)868 bp to the stop codon into the NotI site of pCBI . PCR amplification of this genomic fragment was done with the primers 11 and 12 (see table below). The construct was transformed into fbl17-1 mutant using Agrobacterium tumefaciens GV31O1 with the floral-dip methods . Primers 3 and 4 were used to identify homozygous knock-out mutants rescued by the full genomic construct. The promFBL17∶GUS construct was created by PCR amplifying 868nt of the promoter region with primers 5 and 6 and cloning of the fragment in pENTR1A vector between the EcoRI and XhoI sites. The promoter fragment was then remobilized by LR clonase II recombination (Invitrogen) into pMDC162 . For the BiFc constructs FBL17, ASK11, KRP1, 3, 5 and 7 cDNAs were first amplified by PCR without their STOP codons, cloned into pDONR 201 (except FBL17 which was cloned into pDONR 207) by BP clonase recombination (Invitrogen) before to be transferred into the split-YFP destination vector pSYN and pSYC  by LR clonase reaction (Invitrogen). 35S∶YFP fusion were obtained by remobilizing FBL17, ASK11, and KRPs cDNA from the pDONR vector to the plasmid pEXSG-YFP .
Oligo Sequence (5′→3′)
Total RNA for Q-PCR was extracted from 6 days-old E2Fa-DPa OE and Col-0 wild-type seedlings grown on sterile 1× Murashige and Skoog agar medium with the Plant RNeasy kit (Qiagen). For krp6-1 mutant analysis, total RNA was extracted from inflorescences of krp6-1 homozygous mutant and Col-0 wild-type plants. 1 µg of total RNA was reverse transcribed with the Superscript II RT kit (Invitrogen) and a mixture of random hexamers and oligo dT (18) according to the manufacturer's instruction. PCR was performed using oligos 1 and 2 (FBL17 specific) and oligos 13 and 14 (KRP6 specific) in a total volume of 15 µL SYBR Green Master mix (Roche) on a Lightcycler LC480 apparatus (Roche) according to the manufacturer's instructions. The ACTIN2, AT4G34270 and AT4G26410 genes were used as internal controls for the normalization of the q-PCR.
Developing seeds were prepared from silliques at different days after pollination (DAP) and mounted on microscope slides in a clearing solution of 8∶2∶1 Chloral hydrate: distilled water: glycerol as described in . Observations were performed on a Zeiss Axiophot using 20× and 40× DIC optic. Pollen viability was assessed by mounting pollen in Alexander's stain  and observed by transmitted light microscopy. For DAPI staining of pollen grains, anthers at different stage were dissected and mounted in DAPI solution (DAPI 5 µg/ml, PIPES 50 mM, EGTA 5 mM, NP-40 0,1%, and DMSO 10%) and incubated for 30′ before the observation on a Nikon fluorescent stereo-microscope E800 equipped with a 100× optic. Quantification of DNA content was performed with the software ImageJ (http://rsbweb.nih.gov/ij/) on images taken with constant settings. Background fluorescence values were subtracted to the measure to correct for difference in staining intensity. The obtained measures were normalized against those of generative prophase nuclei from wild type bi-cellular pollen sampled in pre-dehiscent anthers, which are by definition at 2C. Pictures of qrt-1/fbl17-1 and qrt-1 mutant pollen were obtained on a Zeiss LSM 510 Meta confocal microscope as a Z-stack subsequently flattened into a single image in the ImageJ software. GUS staining of anthers at different stages was performed as described in  and the state of pollen development was determined from the pollen DAPI staining taken from the same flower at the same time.
The ASK1 to ASK19 cDNAs cloned as fusions to the GAL4 activation domain and GAL4 binding domain, respectively, in Gateway-compatible pGADT7 and pGBT9 (Clontech) yeast two-hybrid vector have been described in . Full length FBL17 cDNA was mobilized from the entry vector pDONR FBL17 to both pGADT7 and pGBKT7 (Clonetech) with LR clonase II kit (Invitrogen). The yeast strain AH109 (MATa, trp1-901, leu2-3, 112, ura3-52, his3-200, gal4, gal80, LYS2::GAL1UAS-GAL1TATA-HIS3, GAL2UAS-GAL2TATA-ADE2, URA3::MEL1UAS-MEL1TATA-lacZ, MEL1) was transformed with the appropriate combinations of bait and prey vectors. Transformants were selected on synthetic defined (SD)/-Leu/-Trp (SD- LW) medium for 2 days at 30°C. Weak and strong interactions were tested by transferring transformants on SD/-Leu/-Trp/-His (-LWH) with 5 mM 3-amino-1,2,4-triazole (3-AT) and SD/-Leu/-Trp/-Ade (-LWA) media, respectively, allowing growth for 3 days at 30°C.
For infiltration of Nicotiana benthamiana leaves the A. tumefaciens strain GV3101 pMP90RK was used. The A. tumefaciens strains containing the BiFc vectors were infiltrated as described . Infiltration was performed on the abaxial leaf side of two-month-old plants and analyzed 3 to 5 days later.
We thank M. Alioua for quantitative RT-PCR analyses and J. Molinier for some plant crossing experiments.
Conceived and designed the experiments: PG. Performed the experiments: AG NB MN SP HE. Analyzed the data: NB MN TP LDV AS PG. Contributed reagents/materials/analysis tools: AG HE. Wrote the paper: AS PG.
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