Hao Nan, Donnelly Alana J, Dodd Ian B, Shearwin Keith E
Department of Molecular and Biomedical Science, School of Biological Sciences, The University of Adelaide, Adelaide, SA 5005 Australia.
Biophys Rev. 2023 Jun 10;15(3):355-366. doi: 10.1007/s12551-023-01064-7. eCollection 2023 Jun.
In recent years, transcriptional roadblocking has emerged as a crucial regulatory mechanism in gene expression, whereby other DNA-bound obstacles can block the progression of transcribing RNA polymerase (RNAP), leading to RNAP pausing and ultimately dissociation from the DNA template. In this review, we discuss the mechanisms by which transcriptional roadblocks can impede RNAP progression, as well as how RNAP can overcome these obstacles to continue transcription. We examine different DNA-binding proteins involved in transcriptional roadblocking and their biophysical properties that determine their effectiveness in blocking RNAP progression. The catalytically dead CRISPR-Cas (dCas) protein is used as an example of an engineered programmable roadblock, and the current literature in understanding the polarity of dCas roadblocking is also discussed. Finally, we delve into a stochastic model of transcriptional roadblocking and highlight the importance of transcription factor binding kinetics and its resistance to dislodgement by an elongating RNAP in determining the strength of a roadblock.
近年来,转录阻碍已成为基因表达中的一种关键调控机制,即其他与DNA结合的障碍物能够阻止正在转录的RNA聚合酶(RNAP)前进,导致RNAP暂停并最终从DNA模板上解离。在这篇综述中,我们讨论了转录阻碍阻碍RNAP前进的机制,以及RNAP如何克服这些障碍以继续转录。我们研究了参与转录阻碍的不同DNA结合蛋白及其决定其阻碍RNAP前进有效性的生物物理特性。以催化失活的CRISPR-Cas(dCas)蛋白作为工程化可编程阻碍的一个例子,并讨论了当前理解dCas阻碍极性的文献。最后,我们深入探讨了转录阻碍的随机模型,并强调了转录因子结合动力学及其对延伸中的RNAP去除的抗性在确定阻碍强度方面的重要性。