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LARP7对于小鼠减数分裂期间性染色体沉默是必需的。

LARP7 is required for sex chromosome silencing during meiosis in mice.

作者信息

Tando Yukiko, Nonomura Atsuto, Ito-Matsuoka Yumi, Takehara Asuka, Okamura Daiji, Hayashi Yohei, Matsui Yasuhisa

机构信息

Cell Resource Center for Biomedical Research, Institute of Development, Aging and Cancer, Tohoku University, Sendai, Japan.

Graduate School of Life Sciences, Tohoku University, Sendai, Japan.

出版信息

PLoS One. 2024 Dec 5;19(12):e0314329. doi: 10.1371/journal.pone.0314329. eCollection 2024.

Abstract

Meiotic sex chromosome inactivation (MSCI) is an essential event in meiotic progression in mammalian spermatogenesis. We found that La Ribonucleoprotein 7 (LARP7) is involved in MSCI. LARP7 plays a role in fetal germ cells to promote their proliferation, but is once abolished in postnatal gonocytes and re-expressed in spermatocytes at the onset of meiosis. In spermatocytes, LARP7 localizes to the XY body, a compartmentalized chromatin domain on sex chromosomes. In germline-specific Larp7-deficient mice, spermatogenesis is arrested in spermatocytes, and transcription of the genes on sex chromosomes remained active, which suggests failure of meiotic sex chromosome inactivation (MSCI). Furthermore, the XY body in spermatocytes lacking Larp7 shows accumulation of H4K12ac and elimination of H3K9me2, suggesting defective chromatin silencing by abnormal epigenetic controls. These results indicate a new functional role for LARP7 in MSCI.

摘要

减数分裂性染色体失活(MSCI)是哺乳动物精子发生过程中减数分裂进程的一个重要事件。我们发现拉蛋白7(LARP7)参与了MSCI。LARP7在胎儿生殖细胞中发挥作用以促进其增殖,但在出生后生殖母细胞中被消除,并在减数分裂开始时在精母细胞中重新表达。在精母细胞中,LARP7定位于XY小体,这是性染色体上一个分隔的染色质结构域。在生殖系特异性Larp7缺陷小鼠中,精子发生在精母细胞阶段停滞,性染色体上基因的转录仍保持活跃,这表明减数分裂性染色体失活(MSCI)失败。此外,缺乏Larp7的精母细胞中的XY小体显示H4K12ac积累和H3K9me2消除,表明异常表观遗传控制导致染色质沉默缺陷。这些结果表明LARP7在MSCI中具有新的功能作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b06c/11620648/ec240a21f98b/pone.0314329.g001.jpg

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