TDRD1 相分离驱动半软骨间胶结物组装,促进 piRNA 的生物生成和生育能力

IF 10.7 1区 生物学 Q1 CELL BIOLOGY Developmental cell Pub Date : 2024-07-18 DOI:10.1016/j.devcel.2024.06.017
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引用次数: 0

摘要

线粒体间胶结物(IMC)是哺乳动物生殖细胞中位于线粒体群中的一个突出的生殖颗粒。它是 Piwi-interacting RNA(πRNA)生物生成的关键平台;然而,IMC 是如何在线粒体间组装的仍是个谜。在这里,我们发现含 Tudor 结构域的 1 (TDRD1) 通过相分离触发 IMC 组装。TDRD1 的相分离是由其四聚体化的盘卷结构域和二甲基精氨酸结合的 Tudor 结构域共同驱动的,但与其固有无序区无关。TDRD1 被 MILI 募集到线粒体,并依次增强线粒体集聚,通过相分离触发 IMC 组装,从而促进 piRNA 的处理。小鼠 TDRD1 相分离缺陷会破坏 IMC 组装和 piRNA 生物发生,导致转座子去抑制和精子发生停滞。此外,TDRD1相分离在脊椎动物中是保守的,而在无脊椎动物中则不是。总之,我们的研究结果证明了相分离在胚芽颗粒形成中的作用,并在有膜细胞器和无膜细胞器之间建立了联系。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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TDRD1 phase separation drives intermitochondrial cement assembly to promote piRNA biogenesis and fertility

The intermitochondrial cement (IMC) is a prominent germ granule that locates among clustered mitochondria in mammalian germ cells. Serving as a key platform for Piwi-interacting RNA (piRNA) biogenesis; however, how the IMC assembles among mitochondria remains elusive. Here, we identify that Tudor domain-containing 1 (TDRD1) triggers IMC assembly via phase separation. TDRD1 phase separation is driven by the cooperation of its tetramerized coiled-coil domain and dimethylarginine-binding Tudor domains but is independent of its intrinsically disordered region. TDRD1 is recruited to mitochondria by MILI and sequentially enhances mitochondrial clustering and triggers IMC assembly via phase separation to promote piRNA processing. TDRD1 phase separation deficiency in mice disrupts IMC assembly and piRNA biogenesis, leading to transposon de-repression and spermatogenic arrest. Moreover, TDRD1 phase separation is conserved in vertebrates but not in invertebrates. Collectively, our findings demonstrate a role of phase separation in germ granule formation and establish a link between membrane-bound organelles and membrane-less organelles.

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来源期刊
Developmental cell
Developmental cell 生物-发育生物学
CiteScore
18.90
自引率
1.70%
发文量
203
审稿时长
3-6 weeks
期刊介绍: Developmental Cell, established in 2001, is a comprehensive journal that explores a wide range of topics in cell and developmental biology. Our publication encompasses work across various disciplines within biology, with a particular emphasis on investigating the intersections between cell biology, developmental biology, and other related fields. Our primary objective is to present research conducted through a cell biological perspective, addressing the essential mechanisms governing cell function, cellular interactions, and responses to the environment. Moreover, we focus on understanding the collective behavior of cells, culminating in the formation of tissues, organs, and whole organisms, while also investigating the consequences of any malfunctions in these intricate processes.
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