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引导 piRNA 的结合触发 Aub 无结构 N 端区域的甲基化,导致 piRNA 扩增复合物的组装。

Binding of guide piRNA triggers methylation of the unstructured N-terminal region of Aub leading to assembly of the piRNA amplification complex.

机构信息

Division of Biology and Biological Engineering, Pasadena California Institute of Technology, Pasadena, CA, USA.

National Key Laboratory of Plant Molecular Genetics and Shanghai Center for Plant Stress Biology, Center for Excellence in Molecular Plant Sciences, Chinese Academy of Sciences, Shanghai, China.

出版信息

Nat Commun. 2021 Jul 1;12(1):4061. doi: 10.1038/s41467-021-24351-x.

DOI:10.1038/s41467-021-24351-x
PMID:34210982
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8249470/
Abstract

PIWI proteins use guide piRNAs to repress selfish genomic elements, protecting the genomic integrity of gametes and ensuring the fertility of animal species. Efficient transposon repression depends on amplification of piRNA guides in the ping-pong cycle, which in Drosophila entails tight cooperation between two PIWI proteins, Aub and Ago3. Here we show that post-translational modification, symmetric dimethylarginine (sDMA), of Aub is essential for piRNA biogenesis, transposon silencing and fertility. Methylation is triggered by loading of a piRNA guide into Aub, which exposes its unstructured N-terminal region to the PRMT5 methylosome complex. Thus, sDMA modification is a signal that Aub is loaded with piRNA guide. Amplification of piRNA in the ping-pong cycle requires assembly of a tertiary complex scaffolded by Krimper, which simultaneously binds the N-terminal regions of Aub and Ago3. To promote generation of new piRNA, Krimper uses its two Tudor domains to bind Aub and Ago3 in opposite modification and piRNA-loading states. Our results reveal that post-translational modifications in unstructured regions of PIWI proteins and their binding by Tudor domains that are capable of discriminating between modification states is essential for piRNA biogenesis and silencing.

摘要

PIWI 蛋白利用指导 piRNA 抑制自私的基因组元件,保护配子的基因组完整性并确保动物物种的生育能力。转座子的有效抑制依赖于 piRNA 向导在乒乓循环中的扩增,这在果蝇中需要两个 PIWI 蛋白 Aub 和 Ago3 之间的紧密合作。在这里,我们表明 Aub 的翻译后修饰,对称二甲基精氨酸(sDMA),对于 piRNA 的生物发生、转座子沉默和生育能力是必不可少的。甲基化是由 piRNA 向导加载到 Aub 中触发的,这使它的无结构 N 端区域暴露于 PRMT5 甲基化酶复合物。因此,sDMA 修饰是 Aub 加载 piRNA 向导的信号。乒乓循环中 piRNA 的扩增需要由 Krimper 支架构成的三级复合物的组装,Krimper 同时结合 Aub 和 Ago3 的 N 端区域。为了促进新 piRNA 的产生,Krimper 使用其两个 Tudor 结构域结合 Aub 和 Ago3,使其处于相反的修饰和 piRNA 加载状态。我们的结果表明,PIWI 蛋白的无结构区域的翻译后修饰及其与 Tudor 结构域的结合,后者能够区分修饰状态,对于 piRNA 的生物发生和沉默是必不可少的。

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