Mechanisms of Very Long Abortive Transcript Release during Promoter Escape
Author:
Affiliation:
1. Biology Department, Bryn Mawr College, Bryn Mawr, Pennsylvania 19010, United States
2. Program in Biochemistry, Mount Holyoke College, South Hadley, Massachusetts 01075, United States
Funder
Division of Molecular and Cellular Biosciences
Publisher
American Chemical Society (ACS)
Subject
Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.biochem.5b00712
Reference65 articles.
1. In Vitro Studies of Transcript Initiation by Escherichia coli RNA Polymerase. 1. RNA Chain Initiation, Abortive Initiation, and Promoter Escape at Three Bacteriophage Promoters
2. Abortive Initiation and Productive Initiation by RNA Polymerase Involve DNA Scrunching
3. Initial Transcribed Sequence Mutations Specifically Affect Promoter Escape Properties
4. Translocation of the Escherichia coli transcription complex observed in the registers 11 to 20: "jumping" of RNA polymerase and asymmetric expansion and contraction of the "transcription bubble".
5. Stalling of Escherichia coli RNA Polymerase in the +6 to +12 Region in Vivo is Associated with Tight Binding to Consensus Promoter Elements
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