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限制因子减缓早期转录延伸,使RNA聚合酶II在非编码RNA基因座处易于终止。

Restrictor slows early transcription elongation to render RNA polymerase II susceptible to termination at non-coding RNA loci.

作者信息

Mimoso Claudia A, Vlaming Hanneke, de Wagenaar Nathalie P, Adelman Karen

机构信息

Co-first authors.

Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, MA 02115, USA.

出版信息

bioRxiv. 2025 Jan 10:2025.01.08.631787. doi: 10.1101/2025.01.08.631787.

Abstract

The eukaryotic genome is broadly transcribed by RNA polymerase II (RNAPII) to produce protein-coding messenger RNAs (mRNAs) and a repertoire of non-coding RNAs (ncRNAs). Whereas RNAPII is very processive during mRNA transcription, it terminates rapidly during synthesis of many ncRNAs, particularly those that arise opportunistically from accessible chromatin at gene promoters or enhancers. The divergent fates of mRNA versus ncRNA species raise many questions about how RNAPII and associated machineries discriminate functional from spurious transcription. The Restrictor complex, comprised of the RNA binding protein ZC3H4 and RNAPII-interacting protein WDR82, has been implicated in restraining the expression of ncRNAs. However, the determinants of Restrictor targeting and the mechanism of transcription suppression remain unclear. Here, we investigate Restrictor using unbiased sequence screens, and rapid protein degradation followed by nascent RNA sequencing. We find that Restrictor promiscuously suppresses early elongation by RNAPII, but this activity is blocked at most mRNAs by the presence of a 5' splice site. Consequently, Restrictor is a critical determinant of transcription directionality at divergent promoters and prevents transcriptional interference. Finally, our data indicate that rather than directly terminating RNAPII, Restrictor acts by reducing the rate of transcription elongation, rendering RNAPII susceptible to early termination by other machineries.

摘要

真核生物基因组由RNA聚合酶II(RNAPII)广泛转录,以产生蛋白质编码信使RNA(mRNA)和一系列非编码RNA(ncRNA)。虽然RNAPII在mRNA转录过程中具有很高的持续性,但它在许多ncRNA的合成过程中会迅速终止,特别是那些在基因启动子或增强子处从可及染色质中机会性产生的ncRNA。mRNA与ncRNA种类的不同命运引发了许多关于RNAPII及相关机制如何区分功能性转录和假转录的问题。由RNA结合蛋白ZC3H4和与RNAPII相互作用的蛋白WDR82组成的限制因子复合物,已被认为与抑制ncRNA的表达有关。然而,限制因子靶向的决定因素和转录抑制机制仍不清楚。在这里,我们使用无偏向性序列筛选以及快速蛋白质降解结合新生RNA测序来研究限制因子。我们发现限制因子会普遍抑制RNAPII的早期延伸,但这种活性在大多数mRNA处会被5'剪接位点的存在所阻断。因此,限制因子是分歧启动子处转录方向性的关键决定因素,并可防止转录干扰。最后,我们的数据表明,限制因子并非直接终止RNAPII,而是通过降低转录延伸速率起作用,使RNAPII易于被其他机制早期终止。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7814/11741429/9393bb93c714/nihpp-2025.01.08.631787v1-f0001.jpg

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