Direct Detection of Abortive RNA Transcripts in Vivo

被引:84
作者
Goldman, Seth R. [1 ]
Ebright, Richard H. [2 ,3 ]
Nickels, Bryce E. [1 ]
机构
[1] Rutgers State Univ, Dept Genet, Piscataway, NJ 08854 USA
[2] Rutgers State Univ, Waksman Inst, Dept Chem, Piscataway, NJ 08854 USA
[3] Rutgers State Univ, Howard Hughes Med Inst, Piscataway, NJ 08854 USA
关键词
LAC UV5 PROMOTER; POLYMERASE; ESCAPE; INITIATION; VITRO; REGION; SIGMA(70); MECHANISM; ELEMENTS; PROTEIN;
D O I
10.1126/science.1169237
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
During transcription initiation in vitro, prokaryotic and eukaryotic RNA polymerase ( RNAP) can engage in abortive initiation-the synthesis and release of short (2 to 15 nucleotides) RNA transcripts-before productive initiation. It has not been known whether abortive initiation occurs in vivo. Using hybridization with locked nucleic acid probes, we directly detected abortive transcripts in bacteria. In addition, we show that in vivo abortive initiation shows characteristics of in vitro abortive initiation: Abortive initiation increases upon stabilizing interactions between RNAP and either promoter DNA or sigma factor, and also upon deleting elongation factor GreA. Abortive transcripts may have functional roles in regulating gene expression in vivo.
引用
收藏
页码:927 / 928
页数:2
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