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DNA 损伤结合蛋白 2 和 Argonaute 1 通过小 RNA 介导修复紫外线诱导的 DNA 损伤。

Small RNA-mediated repair of UV-induced DNA lesions by the DNA DAMAGE-BINDING PROTEIN 2 and ARGONAUTE 1.

机构信息

Institut de Biologie Moléculaire des Plantes, CNRS, F-67084 Strasbourg, France.

RNA Biology, Department of Biology, Swiss Federal Institute of Technology - Zürich (ETH-Z), Zürich, 8092 Zürich, Switzerland.

出版信息

Proc Natl Acad Sci U S A. 2017 Apr 4;114(14):E2965-E2974. doi: 10.1073/pnas.1618834114. Epub 2017 Mar 21.

DOI:10.1073/pnas.1618834114
PMID:28325872
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5389294/
Abstract

As photosynthetic organisms, plants need to prevent irreversible UV-induced DNA lesions. Through an unbiased, genome-wide approach, we have uncovered a previously unrecognized interplay between Global Genome Repair and small interfering RNAs (siRNAs) in the recognition of DNA photoproducts, prevalently in intergenic regions. Genetic and biochemical approaches indicate that, upon UV irradiation, the DNA DAMAGE-BINDING PROTEIN 2 (DDB2) and ARGONAUTE 1 (AGO1) of form a chromatin-bound complex together with 21-nt siRNAs, which likely facilitates recognition of DNA damages in an RNA/DNA complementary strand-specific manner. The biogenesis of photoproduct-associated siRNAs involves the noncanonical, concerted action of RNA POLYMERASE IV, RNA-DEPENDENT RNA POLYMERASE-2, and DICER-LIKE-4. Furthermore, the chromatin association/dissociation of the DDB2-AGO1 complex is under the control of siRNA abundance and DNA damage signaling. These findings reveal unexpected nuclear functions for DCL4 and AGO1, and shed light on the interplay between small RNAs and DNA repair recognition factors at damaged sites.

摘要

作为光合作用生物,植物需要防止不可逆的紫外线诱导 DNA 损伤。通过一种无偏见的、全基因组的方法,我们揭示了全球基因组修复和小干扰 RNA(siRNA)之间以前未被识别的相互作用,这种相互作用主要发生在基因间区域。遗传和生化方法表明,在 UV 照射后,DNA 损伤结合蛋白 2(DDB2)和 ARGONAUTE 1(AGO1)与 21 个核苷酸的 siRNA 一起形成染色质结合复合物,这可能有助于以 RNA/DNA 互补链特异性的方式识别 DNA 损伤。光产物相关 siRNA 的生物发生涉及非规范的 RNA 聚合酶 IV、RNA 依赖性 RNA 聚合酶-2 和 DICER-LIKE-4 的协同作用。此外,DDB2-AGO1 复合物的染色质结合/解离受 siRNA 丰度和 DNA 损伤信号的控制。这些发现揭示了 DCL4 和 AGO1 的意想不到的核功能,并阐明了小 RNA 和受损部位 DNA 修复识别因子之间的相互作用。