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INTS10-INT11-INT12 形成了核酸结合和解离模块的整合酶的功能模块。

INTS10-INTS13-INTS14 form a functional module of Integrator that binds nucleic acids and the cleavage module.

机构信息

Institute of Molecular Biology and Biophysics, ETH Zurich, Otto-Stern-Weg 5, CH-8093, Zurich, Switzerland.

Institute of Molecular Systems Biology, ETH Zurich, Zurich, Switzerland.

出版信息

Nat Commun. 2020 Jul 9;11(1):3422. doi: 10.1038/s41467-020-17232-2.

Abstract

The Integrator complex processes 3'-ends of spliceosomal small nuclear RNAs (snRNAs). Furthermore, it regulates transcription of protein coding genes by terminating transcription after unstable pausing. The molecular basis for Integrator's functions remains obscure. Here, we show that INTS10, Asunder/INTS13 and INTS14 form a separable, functional Integrator module. The structure of INTS13-INTS14 reveals a strongly entwined complex with a unique chain interlink. Unexpected structural homology to the Ku70-Ku80 DNA repair complex suggests nucleic acid affinity. Indeed, the module displays affinity for DNA and RNA but prefers RNA hairpins. While the module plays an accessory role in snRNA maturation, it has a stronger influence on transcription termination after pausing. Asunder/INTS13 directly binds Integrator's cleavage module via a conserved C-terminal motif that is involved in snRNA processing and required for spermatogenesis. Collectively, our data establish INTS10-INTS13-INTS14 as a nucleic acid-binding module and suggest that it brings cleavage module and target transcripts into proximity.

摘要

整合体复合物处理剪接体小核 RNA(snRNA)的 3'末端。此外,它通过在不稳定暂停后终止转录来调节蛋白质编码基因的转录。整合体功能的分子基础仍然不清楚。在这里,我们表明 INTS10、Asunder/INTS13 和 INTS14 形成一个可分离的、功能性的整合体模块。INTS13-INTs14 的结构揭示了一个紧密缠绕的复合物,具有独特的链连接。出乎意料的与 Ku70-Ku80 DNA 修复复合物的结构同源性表明具有核酸亲和力。事实上,该模块对 DNA 和 RNA 具有亲和力,但更喜欢 RNA 发夹。虽然该模块在 snRNA 成熟过程中起辅助作用,但它对暂停后的转录终止有更强的影响。Asunder/INTS13 通过保守的 C 末端基序直接与整合体的切割模块结合,该基序参与 snRNA 加工,并且是精子发生所必需的。总的来说,我们的数据确立了 INTS10-INTs13-INTs14 作为一个核酸结合模块,并表明它将切割模块和靶转录物拉近。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b1bd/7347597/a083e293f2c9/41467_2020_17232_Fig1_HTML.jpg

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