4sUDRB-seq: measuring genomewide transcriptional elongation rates and initiation frequencies within cells

被引:130
作者
Fuchs, Gilad [1 ]
Voichek, Yoav [2 ]
Benjamin, Sima [3 ]
Gilad, Shlomit [3 ]
Amit, Ido [4 ]
Oren, Moshe [1 ]
机构
[1] Weizmann Inst Sci, Dept Mol Cell Biol, IL-76100 Rehovot, Israel
[2] Weizmann Inst Sci, Dept Mol Genet, IL-76100 Rehovot, Israel
[3] Weizmann Inst Sci, Israel Natl Ctr Personalized Med INCPM, IL-76100 Rehovot, Israel
[4] Weizmann Inst Sci, Dept Immunol, IL-76100 Rehovot, Israel
基金
欧洲研究理事会;
关键词
RNA-POLYMERASE-II; SPLICING IN-VIVO; DROSOPHILA-MELANOGASTER; HIV-1; TAT; C-MYC; GENES; PROMOTERS; COMPLEX; ACTIVATION; RESOLUTION;
D O I
10.1186/gb-2014-15-5-r69
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
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.
引用
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页数:10
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