RNA Polymerase II Collision Interrupts Convergent Transcription

被引:130
|
作者
Hobson, David J. [1 ]
Wei, Wu [2 ,3 ]
Steinmetz, Lars M. [2 ,3 ]
Svejstrup, Jesper Q. [1 ]
机构
[1] Canc Res UK London Res Inst, Clare Hall Labs, Mech Transcript Lab, London EN6 3LD, England
[2] European Mol Biol Lab, Genome Biol Unit, D-69117 Heidelberg, Germany
[3] Stanford Genome Technol Ctr, Palo Alto, CA 94304 USA
基金
欧洲研究理事会; 美国国家卫生研究院;
关键词
COUPLED DNA-REPAIR; PERVASIVE TRANSCRIPTION; STRUCTURAL BASIS; ELONGATION COMPLEX; GENOME; GENES; MECHANISMS; RESOLUTION; STABILITY; ARREST;
D O I
10.1016/j.molcel.2012.08.027
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:365 / 374
页数:10
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