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支架附着因子 B2 蛋白双重核酸识别的结构基础解析。

Insight into the Structural Basis for Dual Nucleic Acid-Recognition by the Scaffold Attachment Factor B2 Protein.

机构信息

Institute for Molecular Biosciences, Biomolecular Resonance Center (BMRZ), Goethe University Frankfurt, Max-von-Laue-Str. 7-9, 60438 Frankfurt, Germany.

IMPRS on Cellular Biophysics, Max-von-Laue-Str. 7-9, 60438 Frankfurt, Germany.

出版信息

Int J Mol Sci. 2023 Feb 7;24(4):3286. doi: 10.3390/ijms24043286.

Abstract

The family of scaffold attachment factor B (SAFB) proteins comprises three members and was first identified as binders of the nuclear matrix/scaffold. Over the past two decades, SAFBs were shown to act in DNA repair, mRNA/(l)ncRNA processing and as part of protein complexes with chromatin-modifying enzymes. SAFB proteins are approximately 100 kDa-sized dual nucleic acid-binding proteins with dedicated domains in an otherwise largely unstructured context, but whether and how they discriminate DNA and RNA binding has remained enigmatic. We here provide the SAFB2 DNA- and RNA-binding SAP and RRM domains in their functional boundaries and use solution NMR spectroscopy to ascribe DNA- and RNA-binding functions. We give insight into their target nucleic acid preferences and map the interfaces with respective nucleic acids on sparse data-derived SAP and RRM domain structures. Further, we provide evidence that the SAP domain exhibits intra-domain dynamics and a potential tendency to dimerize, which may expand its specifically targeted DNA sequence range. Our data provide a first molecular basis of and a starting point towards deciphering DNA- and RNA-binding functions of SAFB2 on the molecular level and serve a basis for understanding its localization to specific regions of chromatin and its involvement in the processing of specific RNA species.

摘要

支架附着因子 B(SAFB)蛋白家族由三个成员组成,最初被鉴定为核基质/支架的结合物。在过去的二十年中,已经表明 SAFB 参与 DNA 修复、mRNA/(l)ncRNA 加工,并作为与染色质修饰酶的蛋白质复合物的一部分发挥作用。SAFB 蛋白大小约为 100 kDa,是具有专用结构域的双核酸结合蛋白,但它们是否以及如何区分 DNA 和 RNA 结合一直是个谜。我们在这里提供了 SAFB2 的 DNA 和 RNA 结合 SAP 和 RRM 结构域及其功能边界,并使用溶液 NMR 光谱来赋予 DNA 和 RNA 结合功能。我们深入了解了它们的靶核酸偏好,并在稀疏数据衍生的 SAP 和 RRM 结构域结构上绘制了与各自核酸的结合界面。此外,我们提供的证据表明,SAP 结构域表现出结构域内的动力学和潜在的二聚化倾向,这可能会扩大其特定靶向的 DNA 序列范围。我们的数据为 SAFB2 在分子水平上解析 DNA 和 RNA 结合功能提供了第一个分子基础,并为理解其在特定染色质区域的定位及其参与特定 RNA 物种的加工提供了基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b879/9958909/583e06c59bbb/ijms-24-03286-g001.jpg

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