Mechanisms of Transcription Laboratory, Clare Hall Laboratories, Cancer Research UK London Research Institute, South Mimms, London EN6 3LD, UK.
Mol Cell. 2012 Nov 9;48(3):365-74. doi: 10.1016/j.molcel.2012.08.027. Epub 2012 Oct 4.
Antisense noncoding transcripts, genes-within-genes, and convergent gene pairs are prevalent among eukaryotes. The existence of such transcription units raises the question of what happens when RNA polymerase II (RNAPII) molecules collide head-to-head. Here we use a combination of biochemical and genetic approaches in yeast to show that polymerases transcribing opposite DNA strands cannot bypass each other. RNAPII stops but does not dissociate upon head-to-head collision in vitro, suggesting that opposing polymerases represent insurmountable obstacles for each other. Head-to-head collision in vivo also results in RNAPII stopping, and removal of collided RNAPII from the DNA template can be achieved via ubiquitylation-directed proteolysis. Indeed, in cells lacking efficient RNAPII polyubiquitylation, the half-life of collided polymerases increases, so that they can be detected between convergent genes. These results provide insight into fundamental mechanisms of gene traffic control and point to an unexplored effect of antisense transcription on gene regulation via polymerase collision.
反义非编码转录本、基因内基因和趋同基因对在真核生物中普遍存在。这些转录单元的存在提出了一个问题,即当 RNA 聚合酶 II(RNAPII)分子头对头碰撞时会发生什么。在这里,我们使用酵母中的生化和遗传方法的组合表明,转录相反 DNA 链的聚合酶不能相互绕过。RNAPII 在体外头对头碰撞时停止但不解离,表明相反的聚合酶彼此代表不可逾越的障碍。体内的头对头碰撞也导致 RNAPII 停止,并且可以通过泛素化指导的蛋白水解从 DNA 模板上去除碰撞的 RNAPII。事实上,在缺乏有效 RNAPII 多泛素化的细胞中,碰撞聚合酶的半衰期增加,因此可以在趋同基因之间检测到它们。这些结果提供了对基因流量控制基本机制的深入了解,并指出了反义转录通过聚合酶碰撞对基因调控的一种未被探索的影响。