Diao Annette J, Su Bonnie G, Vos Seychelle M
Department of Biology, Massachusetts Institute of Technology, Building 68, 31 Ames St., Cambridge, MA 02139, United States.
Department of Biology, Massachusetts Institute of Technology, Building 68, 31 Ames St., Cambridge, MA 02139, United States; Howard Hughes Medical Institute, United States.
J Mol Biol. 2025 Jan 1;437(1):168779. doi: 10.1016/j.jmb.2024.168779. Epub 2024 Sep 4.
RNA polymerase (Pol) II is highly regulated to ensure appropriate gene expression. Early transcription elongation is associated with transient pausing of RNA Pol II in the promoter-proximal region. In multicellular organisms, this pausing is stabilized by the association of transcription elongation factors DRB-sensitivity inducing factor (DSIF) and Negative Elongation Factor (NELF). DSIF is a broadly conserved transcription elongation factor whereas NELF is mostly restricted to the metazoan lineage. Mounting evidence suggests that NELF association with RNA Pol II serves as checkpoint for either release into rapid and productive transcription elongation or premature termination at promoter-proximal pause sites. Here we summarize NELF's roles in promoter-proximal pausing, transcription termination, DNA repair, and signaling based on decades of cell biological, biochemical, and structural work and describe areas for future research.
RNA聚合酶(Pol)II受到高度调控以确保适当的基因表达。早期转录延伸与RNA Pol II在启动子近端区域的短暂暂停相关。在多细胞生物中,转录延伸因子DRB敏感性诱导因子(DSIF)和负延伸因子(NELF)的结合使这种暂停得以稳定。DSIF是一种广泛保守的转录延伸因子,而NELF大多局限于后生动物谱系。越来越多的证据表明,NELF与RNA Pol II的结合充当了一个检查点,决定是释放进入快速且高效的转录延伸,还是在启动子近端暂停位点过早终止。在这里,我们基于数十年的细胞生物学、生物化学和结构研究工作,总结了NELF在启动子近端暂停、转录终止、DNA修复和信号传导中的作用,并描述了未来的研究领域。