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RNA结合蛋白PCBP1通过招募G-四链体特异性解旋酶DHX9来调节转录。

The RNA-binding protein PCBP1 modulates transcription by recruiting the G-quadruplex-specific helicase DHX9.

作者信息

Karam Joseph A Q, Fréreux Cécile, Mohanty Bidyut K, Dalton Annamarie C, Dincman Toros A, Palanisamy Viswanathan, Howley Breege V, Howe Philip H

机构信息

Department of Biochemistry and Molecular Biology, College of Medicine, Medical University of South Carolina, Charleston, South Carolina, USA.

Department of Biochemistry and Molecular Biology, College of Medicine, Medical University of South Carolina, Charleston, South Carolina, USA; Department of Cell Biology and Physiology, Edward Via College of Osteopathic Medicine, Spartanburg, South Carolina, USA.

出版信息

J Biol Chem. 2024 Nov;300(11):107830. doi: 10.1016/j.jbc.2024.107830. Epub 2024 Sep 27.

Abstract

PCBP1, polycytosine (poly(C)) binding protein 1, an RNA and single-stranded DNA (ssDNA) binding protein, binds poly(C) DNA tracts but it remains unclear whether its ability to bind ssDNA contributes to transcriptional regulation. Here, we report that PCBP1's DNA binding sites are enriched at transcription start sites and that by binding to promoter regions, PCBP1 regulates transcription in addition to splicing and translation. At PCBP1 target genes, we show that PCBP1 interacts with several RNA/DNA hybrid (R-loop) associated G-quadruplex resolving helicases. Furthermore, we find that PCBP1 interacts with RNA Helicase A (DHX9) to modulate transcription by regulating DHX9 accumulation and activity. PCBP1 depletion leads to defects in R-loop processing and dysregulation of transcription of PCBP1 target genes. PCBP1's high sequence specificity and interaction with helicases suggest that its mechanism in transcription involves guiding helicases to specific loci during transcription, thereby modulating their activity.

摘要

PCBP1,即多聚胞嘧啶(poly(C))结合蛋白1,是一种RNA和单链DNA(ssDNA)结合蛋白,可结合多聚(C)DNA片段,但尚不清楚其结合ssDNA的能力是否有助于转录调控。在此,我们报告称,PCBP1的DNA结合位点在转录起始位点富集,并且通过结合启动子区域,PCBP1除了调控剪接和翻译外,还调控转录。在PCBP1的靶基因上,我们表明PCBP1与几种RNA/DNA杂交体(R环)相关的G-四链体解旋酶相互作用。此外,我们发现PCBP1与RNA解旋酶A(DHX9)相互作用,通过调节DHX9的积累和活性来调控转录。PCBP1的缺失导致R环加工缺陷和PCBP1靶基因转录失调。PCBP1的高序列特异性及其与解旋酶的相互作用表明,其转录机制涉及在转录过程中将解旋酶引导至特定位点,从而调节其活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9dce/11538862/ce48797e834a/gr1.jpg

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