Okano Yosuke, Aono Naoki, Hiwatashi Yuji, Murata Takashi, Nishiyama Tomoaki, Ishikawa Takaaki, Kubo Minoru, Hasebe Mitsuyasu
National Institute for Basic Biology, Okazaki 444-8585, Japan.
Proc Natl Acad Sci U S A. 2009 Sep 22;106(38):16321-6. doi: 10.1073/pnas.0906997106. Epub 2009 Sep 9.
Land plants have distinct developmental programs in haploid (gametophyte) and diploid (sporophyte) generations. Although usually the two programs strictly alternate at fertilization and meiosis, one program can be induced during the other program. In a process called apogamy, cells of the gametophyte other than the egg cell initiate sporophyte development. Here, we report for the moss Physcomitrella patens that apogamy resulted from deletion of the gene orthologous to the Arabidopsis thaliana CURLY LEAF (PpCLF), which encodes a component of polycomb repressive complex 2 (PRC2). In the deletion lines, a gametophytic vegetative cell frequently gave rise to a sporophyte-like body. This body grew indeterminately from an apical cell with the character of a sporophytic pluripotent stem cell but did not form a sporangium. Furthermore, with continued culture, the sporophyte-like body branched. Sporophyte branching is almost unknown among extant bryophytes. When PpCLF was expressed in the deletion lines once the sporophyte-like bodies had formed, pluripotent stem cell activity was arrested and a sporangium-like organ formed. Supported by the observed pattern of PpCLF expression, these results demonstrate that, in the gametophyte, PpCLF represses initiation of a sporophytic pluripotent stem cell and, in the sporophyte, represses that stem cell activity and induces reproductive organ development. In land plants, branching, along with indeterminate apical growth and delayed initiation of spore-bearing reproductive organs, were conspicuous innovations for the evolution of a dominant sporophyte plant body. Our study provides insights into the role of PRC2 gene regulation for sustaining evolutionary innovation in land plants.
陆生植物在单倍体(配子体)和二倍体(孢子体)世代具有不同的发育程序。虽然通常这两个程序在受精和减数分裂时严格交替,但一个程序可以在另一个程序期间被诱导。在一个称为无配子生殖的过程中,除卵细胞外的配子体细胞启动孢子体发育。在此,我们报道对于小立碗藓而言,无配子生殖是由与拟南芥卷曲叶基因(PpCLF)直系同源的基因缺失导致的,该基因编码多梳抑制复合体2(PRC2)的一个组分。在缺失系中,一个配子体营养细胞经常产生一个类似孢子体的结构。这个结构从具有孢子体多能干细胞特征的顶端细胞开始无限生长,但不形成孢子囊。此外,随着持续培养,类似孢子体的结构会分支。现存苔藓植物中几乎不存在孢子体分支现象。当类似孢子体的结构形成后在缺失系中表达PpCLF时,多能干细胞活性被阻断,一个类似孢子囊的器官形成。这些结果在观察到的PpCLF表达模式的支持下,表明在配子体中,PpCLF抑制孢子体多能干细胞的起始,而在孢子体中,抑制该干细胞活性并诱导生殖器官发育。在陆生植物中,分支以及无限的顶端生长和产生孢子的生殖器官起始延迟,是优势孢子体植物主体进化过程中显著的创新。我们的研究为PRC2基因调控在维持陆生植物进化创新中的作用提供了见解。