Fuchs Gilad, Voichek Yoav, Benjamin Sima, Gilad Shlomit, Amit Ido, Oren Moshe
Genome Biol. 2014 May 9;15(5):R69. doi: 10.1186/gb-2014-15-5-r69.
Although transcriptional elongation by RNA polymerase II is coupled with many RNA-related processes, genomewide elongation rates remain unknown. We describe a method, called 4sUDRB-seq, based on reversible inhibition of transcription elongation coupled with tagging newly transcribed RNA with 4-thiouridine and high throughput sequencing to measure simultaneously with high confidence genome-wide transcription elongation rates in cells. We find that most genes are transcribed at about 3.5 Kb/min, with elongation rates varying between 2 Kb/min and 6 Kb/min. 4sUDRB-seq can facilitate genomewide exploration of the involvement of specific elongation factors in transcription and the contribution of deregulated transcription elongation to various pathologies.
尽管RNA聚合酶II介导的转录延伸与许多RNA相关过程相关联,但全基因组范围的延伸速率仍然未知。我们描述了一种称为4sUDRB-seq的方法,该方法基于转录延伸的可逆抑制,同时用4-硫尿苷标记新转录的RNA,并结合高通量测序,以在细胞中同时以高置信度测量全基因组范围的转录延伸速率。我们发现,大多数基因的转录速率约为3.5 kb/min,延伸速率在2 kb/min至6 kb/min之间变化。4sUDRB-seq有助于在全基因组范围内探索特定延伸因子在转录中的作用,以及转录延伸失调对各种病理的影响。