Johnston Amal J, Matveeva Elena, Kirioukhova Olga, Grossniklaus Ueli, Gruissem Wilhelm
Plant Biotechnology, Institute of Plant Sciences & Zurich-Basel Plant Science Center, ETH Zurich, Universitätstrasse 2, CH-8092 Zurich, Switzerland.
Curr Biol. 2008 Nov 11;18(21):1680-6. doi: 10.1016/j.cub.2008.09.026. Epub 2008 Oct 30.
Unlike animals that produce gametes upon differentiation of meiotic products, plants develop haploid male and female gametophytes that differentiate gametes such as sperm, egg and central cells, and accessory cells [1, 2]. Both gametophytes participate in double fertilization and give rise to the next sporophytic generation. Little is known about the function of cell-cycle genes in differentiation and development of gametophytes and in reproduction [1, 2]. RETINOBLASTOMA RELATED (RBR) is a plant homolog of the tumor suppressor Retinoblastoma (pRb), which is primarily known as negative regulator of the cell cycle [3]. We show that RBR is required for cell differentiation of male and female gametophytes in Arabidopsis and that loss of RBR perturbs expression levels of the evolutionarily ancient Polycomb Repressive Complex 2 (PRC2) subunits and their modifiers encoding PRC2 subunits or DNA METHYLTRANSFERASE 1 (MET1) [4-6], exemplifying convergent evolution involving the RBR-PRC2-MET1 regulatory pathways. In addition, RBR binds MET1, and maintenance of heterochromatin in central cells, a mechanism that is likely mediated by MET1[7, 8], is impaired in the absence of RBR. Surprisingly, PRC2-specific H3K27-trimethylation activity represses paternal RBR allele, suggesting a functional role for a dynamic and reciprocal RBR-PRC2 regulatory circuit in cellular differentiation and reproductive development.
与通过减数分裂产物分化产生配子的动物不同,植物发育出单倍体雄配子体和雌配子体,它们分化出精子、卵细胞和中央细胞等配子以及辅助细胞[1,2]。两种配子体都参与双受精并产生下一代孢子体世代。关于细胞周期基因在配子体分化和发育以及繁殖中的功能,人们了解甚少[1,2]。视网膜母细胞瘤相关蛋白(RBR)是肿瘤抑制因子视网膜母细胞瘤(pRb)的植物同源物,主要作为细胞周期的负调控因子为人所知[3]。我们发现,拟南芥中雄配子体和雌配子体的细胞分化需要RBR,RBR的缺失会扰乱进化上古老的多梳抑制复合体2(PRC2)亚基及其编码PRC2亚基或DNA甲基转移酶1(MET1)的修饰因子的表达水平[4 - 6],这体现了涉及RBR - PRC2 - MET1调控途径的趋同进化。此外,RBR与MET1结合,在没有RBR的情况下,中央细胞中异染色质的维持(一种可能由MET1介导的机制)[7,8]会受到损害。令人惊讶的是,PRC2特异性的H3K27三甲基化活性会抑制父本RBR等位基因,这表明动态且相互的RBR - PRC2调控回路在细胞分化和生殖发育中具有功能性作用。