Lacadie Scott A, Ibrahim Mahmoud M, Gokhale Sucheta A, Ohler Uwe
Berlin Institute for Medical Systems Biology, Max Delbrück Center for Molecular Medicine, Berlin, Germany.
Berlin Institute of Health (BIH), Germany.
FEBS J. 2016 Dec;283(23):4214-4222. doi: 10.1111/febs.13747. Epub 2016 May 11.
Genome-wide datasets measuring nascent RNA have revealed that active human promoters frequently display divergent transcription, generating a stable mRNA in the forward direction toward the gene and a typically unstable one in the reverse direction away from the gene. Recent work has shown that these transcripts originate from two distinct core promoters within a single nucleosome-free region (NFR). Different levels of forward and reverse activity lead to a wide range of directionality for promoter NFRs. Importantly, directionality is also reflected in the epigenetic modifications of nucleosomes immediately adjacent to the NFR. Here, we review the current literature pertaining to divergent transcription from promoter NFRs and its association with combinatorial histone post-translational modifications, or chromatin states, on upstream and downstream nucleosomes. Finally, we discuss several models to interpret the directionality of promoter chromatin states.
全基因组范围内测量新生RNA的数据集表明,活跃的人类启动子经常表现出双向转录,在朝向基因的正向产生稳定的mRNA,而在背离基因的反向产生通常不稳定的mRNA。最近的研究表明,这些转录本源自单个无核小体区域(NFR)内的两个不同的核心启动子。正向和反向活性的不同水平导致启动子NFR的方向性范围很广。重要的是,方向性也反映在紧邻NFR的核小体的表观遗传修饰中。在这里,我们回顾了当前与启动子NFR的双向转录及其与上游和下游核小体上组合性组蛋白翻译后修饰或染色质状态的关联相关的文献。最后,我们讨论了几种解释启动子染色质状态方向性的模型。