Department of Biology and Zurich-Basel Plant Science Center, ETH Zurich, Zurich, Switzerland.
PLoS Genet. 2010 Jun 17;6(6):e1000988. doi: 10.1371/journal.pgen.1000988.
The plant life cycle alternates between two distinct multi-cellular generations, the reduced gametophytes and the dominant sporophyte. Little is known about how generation-specific cell fate, differentiation, and development are controlled by the core regulators of the cell cycle. In Arabidopsis, RETINOBLASTOMA RELATED (RBR), an evolutionarily ancient cell cycle regulator, controls cell proliferation, differentiation, and regulation of a subset of Polycomb Repressive Complex 2 (PRC2) genes and METHYLTRANSFERASE 1 (MET1) in the male and female gametophytes, as well as cell fate establishment in the male gametophyte. Here we demonstrate that RBR is also essential for cell fate determination in the female gametophyte, as revealed by loss of cell-specific marker expression in all the gametophytic cells that lack RBR. Maintenance of genome integrity also requires RBR, because diploid plants heterozygous for rbr (rbr/RBR) produce an abnormal portion of triploid offspring, likely due to gametic genome duplication. While the sporophyte of the diploid mutant plants phenocopied wild type due to the haplosufficiency of RBR, genetic analysis of tetraploid plants triplex for rbr (rbr/rbr/rbr/RBR) revealed that RBR has a dosage-dependent pleiotropic effect on sporophytic development, trichome differentiation, and regulation of PRC2 subunit genes CURLY LEAF (CLF) and VERNALIZATION 2 (VRN2), and MET1 in leaves. There were, however, no obvious cell cycle and cell proliferation defects in these plant tissues, suggesting that a single functional RBR copy in tetraploids is capable of maintaining normal cell division but is not sufficient for distinct differentiation and developmental processes. Conversely, in leaves of mutants in sporophytic PRC2 subunits, trichome differentiation was also affected and expression of RBR and MET1 was reduced, providing evidence for a RBR-PRC2-MET1 regulatory feedback loop involved in sporophyte development. Together, dosage-sensitive RBR function and its genetic interaction with PRC2 genes and MET1 must have been recruited during plant evolution to control distinct generation-specific cell fate, differentiation, and development.
植物的生命周期在两个明显不同的多细胞世代之间交替,即简化的配子体和占优势的孢子体。人们对核心细胞周期调节剂如何控制世代特异性细胞命运、分化和发育知之甚少。在拟南芥中,视网膜母细胞瘤相关(RBR)是一种古老的细胞周期调节剂,它控制着细胞增殖、分化以及雄性和雌性配子体中多梳抑制复合物 2(PRC2)基因和甲基转移酶 1(MET1)的调控,还控制着雄性配子体中的细胞命运建立。在这里,我们证明 RBR 对于雌性配子体中的细胞命运决定也是必不可少的,因为在缺乏 RBR 的所有配子体细胞中,细胞特异性标记的表达都丧失了。基因组完整性的维持也需要 RBR,因为杂合 rbr(rbr/RBR)的二倍体植物产生异常部分的三倍体后代,这可能是由于配子体基因组的复制。虽然二倍体突变体植物的孢子体由于 RBR 的单倍体充足而表现出与野生型相似的表型,但对四倍体植物 trplex for rbr(rbr/rbr/rbr/RBR)的遗传分析表明,RBR 对孢子体发育、毛状体分化以及 PRC2 亚基基因卷曲叶(CLF)和春化 2(VRN2)和 MET1 在叶片中的调控具有剂量依赖性的多效性效应。然而,在这些植物组织中没有明显的细胞周期和细胞增殖缺陷,这表明四倍体中单个功能性 RBR 拷贝能够维持正常的细胞分裂,但不足以进行不同的分化和发育过程。相反,在孢子体 PRC2 亚基突变体的叶片中,毛状体分化也受到影响,RBR 和 MET1 的表达减少,这为参与孢子体发育的 RBR-PRC2-MET1 调控反馈环提供了证据。总之,剂量敏感的 RBR 功能及其与 PRC2 基因和 MET1 的遗传相互作用,在植物进化过程中必须被招募来控制不同的世代特异性细胞命运、分化和发育。