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保守的 RNA 解旋酶 YTHDC2 调控生殖细胞从增殖到分化的转变。

The conserved RNA helicase YTHDC2 regulates the transition from proliferation to differentiation in the germline.

机构信息

Department of Developmental Biology, Stanford University School of Medicine, Stanford, United States.

Center for Personal Dynamic Regulomes, Stanford University School of Medicine, Stanford, United States.

出版信息

Elife. 2017 Oct 31;6:e26116. doi: 10.7554/eLife.26116.

Abstract

The switch from mitosis to meiosis is the key event marking onset of differentiation in the germline stem cell lineage. In , the translational repressor Bgcn is required for spermatogonia to stop mitosis and transition to meiotic prophase and the spermatocyte state. Here we show that the mammalian Bgcn homolog YTHDC2 facilitates a clean switch from mitosis to meiosis in mouse germ cells, revealing a conserved role for YTHDC2 in this critical cell fate transition. YTHDC2-deficient male germ cells enter meiosis but have a mixed identity, maintaining expression of Cyclin A2 and failing to properly express many meiotic markers. Instead of continuing through meiotic prophase, the cells attempt an abnormal mitotic-like division and die. YTHDC2 binds multiple transcripts including and other mitotic transcripts, binds specific piRNA precursors, and interacts with RNA granule components, suggesting that proper progression of germ cells through meiosis is licensed by YTHDC2 through post-transcriptional regulation.

摘要

有丝分裂向减数分裂的转变是生殖干细胞谱系分化起始的关键事件。在 中,翻译抑制剂 Bgcn 对于精原细胞停止有丝分裂并向减数分裂前期和精母细胞状态转变是必需的。在这里,我们表明哺乳动物 Bgcn 同源物 YTHDC2 促进了小鼠生殖细胞中从有丝分裂到减数分裂的顺利转变,揭示了 YTHDC2 在这个关键的细胞命运转变中的保守作用。YTHDC2 缺陷型精原细胞进入减数分裂,但具有混合身份,保持细胞周期蛋白 A2 的表达,并且不能正确表达许多减数分裂标记物。这些细胞不是继续进行减数分裂前期,而是试图进行异常的类似于有丝分裂的分裂,然后死亡。YTHDC2 结合多种转录本,包括 和其他有丝分裂转录本,结合特定的 piRNA 前体,并与 RNA 颗粒成分相互作用,这表明 YTHDC2 通过转录后调控来许可生殖细胞正确地通过减数分裂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a5a5/5703642/2a959a6c554e/elife-26116-fig1.jpg

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