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敏感的piRNA报告基因鉴定出多个参与piRNA介导的基因沉默的RNA加工因子。

Sensitized piRNA reporter identifies multiple RNA processing factors involved in piRNA-mediated gene silencing.

作者信息

Brown Jordan, Zhang Donglei, Chen Wenjun, Lee Heng-Chi

机构信息

Department of Molecular Genetics and Cell Biology, University of Chicago, Chicago, IL 60637, USA.

Present address: Department of Laboratory Medicine, Third Affiliated Hospital of Sun Yat-Sen University, Guangzhou, China.

出版信息

bioRxiv. 2023 Jan 22:2023.01.22.525052. doi: 10.1101/2023.01.22.525052.

DOI:10.1101/2023.01.22.525052
PMID:36712000
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9882300/
Abstract

Metazoans guard their germlines against transposons and other foreign transcripts with PIWI-interacting RNAs (piRNAs). Due to the robust heritability of the silencing initiated by piRNAs in , previous screens using were strongly biased to uncover members of this pathway in the maintenance process but not in the initiation process. To identify novel piRNA pathway members, we have utilized a sensitized reporter strain which detects defects in initiation, amplification, or regulation of piRNA silencing. Using our reporter, we have identified Integrator complex subunits, nuclear pore components, protein import components, and pre-mRNA splicing factors as essential for piRNA-mediated gene silencing. We found the snRNA processing cellular machine termed the Integrator complex is required for both type I and type II piRNA production. Notably, we identified a role for nuclear pore and nucleolar components in promoting the perinuclear localization of anti-silencing CSR-1 Argonaute, as well as a role for Importin factor IMA-3 in nuclear localization of silencing Argonaute HRDE-1. Together, we have shown that piRNA silencing is dependent on evolutionarily ancient RNA processing machinery that has been co-opted to function in the piRNA mediated genome surveillance pathway.

摘要

后生动物利用与PIWI相互作用的RNA(piRNA)来保护其生殖系免受转座子和其他外来转录本的影响。由于piRNA引发的沉默具有强大的遗传性,之前使用[具体方法]的筛选在很大程度上偏向于揭示该途径在维持过程而非起始过程中的成员。为了鉴定新的piRNA途径成员,我们利用了一种敏感的报告菌株,该菌株可检测piRNA沉默起始、扩增或调控中的缺陷。使用我们的报告菌株,我们鉴定出整合酶复合物亚基、核孔成分、蛋白质导入成分和前体mRNA剪接因子对piRNA介导的基因沉默至关重要。我们发现被称为整合酶复合物的snRNA加工细胞机器对于I型和II型piRNA的产生都是必需的。值得注意的是,我们确定了核孔和核仁成分在促进抗沉默CSR-1 Argonaute的核周定位中的作用,以及输入蛋白因子IMA-3在沉默Argonaute HRDE-1的核定位中的作用。总之,我们表明piRNA沉默依赖于进化上古老的RNA加工机器,该机器已被用于在piRNA介导的基因组监测途径中发挥作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ec3/9882300/96d2780a0f10/nihpp-2023.01.22.525052v1-f0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ec3/9882300/616cca77ec24/nihpp-2023.01.22.525052v1-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ec3/9882300/9a46c93d0e1f/nihpp-2023.01.22.525052v1-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ec3/9882300/f28c0e9d13bd/nihpp-2023.01.22.525052v1-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ec3/9882300/d363f773111a/nihpp-2023.01.22.525052v1-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ec3/9882300/73ba4d4aeb8f/nihpp-2023.01.22.525052v1-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ec3/9882300/96d2780a0f10/nihpp-2023.01.22.525052v1-f0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ec3/9882300/616cca77ec24/nihpp-2023.01.22.525052v1-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ec3/9882300/9a46c93d0e1f/nihpp-2023.01.22.525052v1-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ec3/9882300/f28c0e9d13bd/nihpp-2023.01.22.525052v1-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ec3/9882300/d363f773111a/nihpp-2023.01.22.525052v1-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ec3/9882300/73ba4d4aeb8f/nihpp-2023.01.22.525052v1-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ec3/9882300/96d2780a0f10/nihpp-2023.01.22.525052v1-f0006.jpg

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本文引用的文献

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