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Maintaining Sufficient Nanos Is a Critical Function for Polar Granule Component in the Specification of Primordial Germ Cells

机译:维持足够的纳米粒子是原始生殖细胞规范中极性颗粒成分的关键功能

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pPrimordial germ cells (PGC) are the precursors of germline stem cells. In iDrosophila/i, PGC specification is thought to require transcriptional quiescence and three genes, ipolar granule component/i (ipgc/i), inanos/i (inos/i), and igerm cell less/i (igcl/i) function to downregulate Pol II transcription. While it is not understood how inos/i or igcl/i represses transcription, ipgc/i does so by inhibiting the transcription elongation factor b (P-TEFb), which is responsible for phosphorylating Ser2 residues in the heptad repeat of the C-terminal domain (CTD) of the largest Pol II subunit. In the studies reported here, we demonstrate that inos/i are a critical regulatory target of ipgc/i. We show that a substantial fraction of the PGCs in ipgc/i embryos have greatly reduced levels of Nos protein and exhibit phenotypes characteristic of inos/i PGCs. Lastly, restoring germ cella€“specific expression of Nos is sufficient to ameliorate the ipgc/i phenotype./p
机译:>原始生殖细胞(PGC)是生殖干细胞的前体。在果蝇中,认为PGC规范需要转录静止和三个基因,即极性颗粒成分( pgc ), nanos ( nos )和生殖细胞少( gcl )的功能下调Pol II转录。虽然尚不了解 nos 或 gcl 如何抑制转录,但 pgc 却通过抑制转录延伸因子b(P-TEFb)来抑制转录。负责磷酸化最大的Pol II亚基C末端结构域(CTD)的七肽重复序列中的Ser2残基。在这里报道的研究中,我们证明 nos 是 pgc 的关键监管目标。我们表明,在 pgc 胚胎中,大部分PGCs的Nos蛋白水平大大降低,并表现出 nos PGCs的表型。最后,恢复生殖细胞的Nos特异性表达足以改善 pgc 表型。

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