Single-strand promoter traps for bacterial RNA polymerase
Author:
Affiliation:
1. Institute of Molecular Genetics, Russian Academy of Sciences, Moscow 123182, Russia
2. Department of Molecular Biology, Biological Faculty, Moscow State University, Moscow 119991, Russia
Abstract
Publisher
Portland Press Ltd.
Subject
Cell Biology,Molecular Biology,Biochemistry
Link
https://portlandpress.com/biochemj/article-pdf/452/2/241/675891/bj4520241.pdf
Reference40 articles.
1. Advances in bacterial promoter recognition and its control by factors that do not bind DNA;Haugen;Nat. Rev. Microbiol.,2008
2. A basal promoter element recognized by free RNA polymerase σ subunit determines promoter recognition by RNA polymerase holoenzyme;Feklistov;Mol. Cell,2006
3. rRNA promoter regulation by nonoptimal binding of σ region 1.2: an additional recognition element for RNA polymerase;Haugen;Cell,2006
4. Structural modules of RNA polymerase required for transcription from promoters containing downstream basal promoter element GGGA;Barinova;J. Biol. Chem.,2008
5. Fine structure of the promoter–σ region 1.2 interaction;Haugen;Proc. Natl. Acad. Sci. U.S.A.,2008
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1. Role of Interactions of the CRE Region of Escherichia coli RNA Polymerase with Nontemplate DNA during Promoter Escape;Biochemistry (Moscow);2020-06-29
2. Dual role of the σ factor in primer RNA synthesis by bacterial RNA polymerase;FEBS Letters;2018-12-20
3. Site-specific aptamer inhibitors of Thermus RNA polymerase;Biochemical and Biophysical Research Communications;2018-01
4. Single-Stranded DNA Aptamers for Functional Probing of Bacterial RNA Polymerase;Methods in Molecular Biology;2015
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