Martinho Rui Gonçalo, Kunwar Prabhat S, Casanova Jordi, Lehmann Ruth
Developmental Genetics Program, The Skirball Institute and Howard Hughes Medical Institute, New York University School of Medicine, New York, NY 10016, USA.
Curr Biol. 2004 Jan 20;14(2):159-65. doi: 10.1016/j.cub.2003.12.036.
RNApolII-dependent transcription is repressed in primordial germ cells of many animals during early development and is thought to be important for maintenance of germline fate by preventing somatic differentiation. Germ cell transcriptional repression occurs concurrently with inhibition of phosphorylation in the carboxy-terminal domain (CTD) of RNApolII, as well as with chromatin remodeling. The precise mechanisms involved are unknown. Here, we present evidence that a noncoding RNA transcribed by the gene polar granule component (pgc) regulates transcriptional repression in Drosophila germ cells. Germ cells lacking pgc RNA express genes important for differentiation of nearby somatic cells and show premature phosphorylation of RNApolII. We further show that germ cells lacking pgc show increased levels of K4, but not K9 histone H3 methylation, and that the chromatin remodeling Swi/Snf complex is required for a second stage in germ cell transcriptional repression. We propose that a noncoding RNA controls transcription in early germ cells by blocking the transition from preinitiation to transcriptional elongation. We further show that repression of somatic differentiation signals mediated by the Torso receptor-tyrosine kinase is important for germline development.
在许多动物的早期发育过程中,RNA聚合酶II(RNApolII)依赖性转录在原始生殖细胞中受到抑制,并且被认为通过防止体细胞分化对于维持生殖系命运很重要。生殖细胞转录抑制与RNApolII羧基末端结构域(CTD)中的磷酸化抑制以及染色质重塑同时发生。其中涉及的精确机制尚不清楚。在这里,我们提供证据表明由极性颗粒成分(pgc)基因转录的非编码RNA调节果蝇生殖细胞中的转录抑制。缺乏pgc RNA的生殖细胞表达对附近体细胞分化重要的基因,并显示RNApolII的过早磷酸化。我们进一步表明,缺乏pgc的生殖细胞显示H3组蛋白K4甲基化水平增加,但K9甲基化水平未增加,并且染色质重塑Swi/Snf复合物是生殖细胞转录抑制第二阶段所必需的。我们提出,一种非编码RNA通过阻断从起始前到转录延伸的转变来控制早期生殖细胞中的转录。我们还表明,由躯干受体酪氨酸激酶介导的体细胞分化信号的抑制对于生殖系发育很重要。