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首页> 外文期刊>Nucleic Acids Research >Cohesin SA1 and SA2 are RNA binding proteins that localize to RNA containing regions on DNA
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Cohesin SA1 and SA2 are RNA binding proteins that localize to RNA containing regions on DNA

机译:Cohesin SA1和SA2是RNA结合蛋白,其定位于含有DNA上的RNA的RNA

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摘要

Cohesin SA1 (STAG1) and SA2 (STAG2) are key components of the cohesin complex. Previous studies have highlighted the unique contributions by SA1 and SA2 to 3D chromatin organization, DNA replication fork progression, and DNA double-strand break (DSB) repair. Recently, we discovered that cohesin SA1 and SA2 are DNA binding proteins. Given the recently discovered link between SA2 and RNA-mediated biological pathways, we investigated whether or not SA1 and SA2 directly bind to RNA using a combination of bulk biochemical assays and single-molecule techniques, including atomic force microscopy (AFM) and the DNA tightrope assay. We discovered that both SA1 and SA2 bind to various RNA containing substrates, including ssRNA, dsRNA, RNA:DNA hybrids, and R-loops. Importantly, both SA1 and SA2 localize to regions on dsDNA that contain RNA. We directly compared the SA1/SA2 binding and R-loops sites extracted from Chromatin Immunoprecipitation sequencing (ChIP-seq) and DNA-RNA Immunoprecipitation sequencing (DRIP-Seq) data sets, respectively. This analysis revealed that SA1 and SA2 binding sites overlap significantly with R-loops. The majority of R-loop-localized SA1 and SA2 are also sites where other subunits of the cohesin complex bind. These results provide a new direction for future investigation of the diverse biological functions of SA1 and SA2.
机译:Cohesin SA1(Stag1)和SA2(Stag2)是Cohesin复合物的关键部件。以前的研究突出了SA1和SA2对3D染色质组织,DNA复制叉进展和DNA双链断裂(DSB)修复的独特贡献。最近,我们发现Cohesin Sa1和Sa 2是DNA结合蛋白。鉴于SA2和RNA介导的生物途径之间的最近发现的联系,我们研究了SA1和SA2是否使用大量生物化学测定和单分子技术的组合直接与RNA结合,包括原子力显微镜(AFM)和DNA Tightrope测定。我们发现,SA1和SA2都与含有含有SSRNA,DSRNA,RNA:DNA杂种和R环的含有底物的各种RNA。重要的是,SA1和SA2都定位于含有RNA的DSDNA上的区域。我们直接比较了从染色质免疫沉淀序列(Chip-SEQ)和DNA-RNA免疫沉淀测序(DRIP-SEQ)数据集中提取的SA1 / SA2结合和R-LOPS位点。该分析显示SA1和SA2结合位点与R圈重叠。大多数R环局部化SA1和SA2也是CONENIN复合物的其他亚基结合的位点。这些结果为未来调查SA1和SA2的不同生物功能提供了新的方向。

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  • 来源
    《Nucleic Acids Research》 |2020年第10期|共17页
  • 作者单位

    North Carolina State Univ Phys Dept Raleigh NC 27695 USA;

    Rice Univ Dept BioSci Houston TX 77251 USA;

    North Carolina State Univ Phys Dept Raleigh NC 27695 USA;

    North Carolina State Univ Phys Dept Raleigh NC 27695 USA;

    Univ Texas Hlth San Antonio Greehey Childrens Canc Res Inst San Antonio TX 78229 USA;

    Rice Univ Dept BioSci Houston TX 77251 USA;

    North Carolina State Univ Phys Dept Raleigh NC 27695 USA;

    Rice Univ Dept BioSci Houston TX 77251 USA;

    North Carolina State Univ Phys Dept Raleigh NC 27695 USA;

    Univ Texas Hlth San Antonio Greehey Childrens Canc Res Inst San Antonio TX 78229 USA;

    Univ Osnabruck Div Biophys Barbarstr 11 D-49076 Osnabruck Germany;

    Univ Osnabruck Div Biophys Barbarstr 11 D-49076 Osnabruck Germany;

    North Carolina State Univ Phys Dept Raleigh NC 27695 USA;

    Univ Texas Hlth San Antonio Greehey Childrens Canc Res Inst San Antonio TX 78229 USA;

    Rice Univ Dept BioSci Houston TX 77251 USA;

    North Carolina State Univ Phys Dept Raleigh NC 27695 USA;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 生物化学;
  • 关键词

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