Literature DB >> 15068808

Forward translocation is the natural pathway of RNA release at an intrinsic terminator.

Thomas J Santangelo1, Jeffrey W Roberts.   

Abstract

Intrinsic terminators of bacterial RNA polymerase are small (< approximately 30 bp) sequences containing a dyad symmetry that encodes a hairpin in the RNA, followed immediately by a uridine-rich stretch of 5-9 nucleotides just before the site of RNA release. Formation of the RNA hairpin destabilizes the elongation complex, leading to transcript release. We test a model in which hair-pin formation drives RNA polymerase and the melted DNA bubble downstream without transcript elongation, thus releasing the transcript from its enclosure within the enzyme as an RNA/DNA hybrid. We show that blocking downstream translocation of RNAP and preventing downstream DNA unwinding both inhibit transcript release. We argue that translocation of RNA polymerase is essential and that translocation of the bubble stimulates, but is not required, for RNA release; we conclude that forward translocation is the natural pathway of RNA release at an intrinsic terminator.

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Year:  2004        PMID: 15068808     DOI: 10.1016/s1097-2765(04)00154-6

Source DB:  PubMed          Journal:  Mol Cell        ISSN: 1097-2765            Impact factor:   17.970


  54 in total

1.  Allosteric Activation of Bacterial Swi2/Snf2 (Switch/Sucrose Non-fermentable) Protein RapA by RNA Polymerase: BIOCHEMICAL AND STRUCTURAL STUDIES.

Authors:  Smita Kakar; Xianyang Fang; Lucyna Lubkowska; Yan Ning Zhou; Gary X Shaw; Yun-Xing Wang; Ding Jun Jin; Mikhail Kashlev; Xinhua Ji
Journal:  J Biol Chem       Date:  2015-08-13       Impact factor: 5.157

2.  Role of forward translocation in nucleoside triphosphate phosphohydrolase I (NPH I)-mediated transcription termination of vaccinia virus early genes.

Authors:  Jessica Tate; Paul Gollnick
Journal:  J Biol Chem       Date:  2011-11-07       Impact factor: 5.157

3.  Probing conformational changes in T7 RNA polymerase during initiation and termination by using engineered disulfide linkages.

Authors:  Kaiyu Ma; Dmitry Temiakov; Michael Anikin; William T McAllister
Journal:  Proc Natl Acad Sci U S A       Date:  2005-11-21       Impact factor: 11.205

4.  Pulling on the nascent RNA during transcription does not alter kinetics of elongation or ubiquitous pausing.

Authors:  Ravindra V Dalal; Matthew H Larson; Keir C Neuman; Jeff Gelles; Robert Landick; Steven M Block
Journal:  Mol Cell       Date:  2006-07-21       Impact factor: 17.970

Review 5.  A contemporary view of coronavirus transcription.

Authors:  Stanley G Sawicki; Dorothea L Sawicki; Stuart G Siddell
Journal:  J Virol       Date:  2006-08-23       Impact factor: 5.103

6.  Manipulating archaeal systems to permit analyses of transcription elongation-termination decisions in vitro.

Authors:  Alexandra M Gehring; Thomas J Santangelo
Journal:  Methods Mol Biol       Date:  2015

7.  Dissociation of halted T7 RNA polymerase elongation complexes proceeds via a forward-translocation mechanism.

Authors:  Yi Zhou; Deanna M Navaroli; Metewo Selase Enuameh; Craig T Martin
Journal:  Proc Natl Acad Sci U S A       Date:  2007-06-06       Impact factor: 11.205

8.  A transcription antiterminator constructs a NusA-dependent shield to the emerging transcript.

Authors:  Smita Shankar; Asma Hatoum; Jeffrey W Roberts
Journal:  Mol Cell       Date:  2007-09-21       Impact factor: 17.970

9.  Role of DNA bubble rewinding in enzymatic transcription termination.

Authors:  Joo-Seop Park; Jeffrey W Roberts
Journal:  Proc Natl Acad Sci U S A       Date:  2006-03-21       Impact factor: 11.205

Review 10.  Transcription termination by the eukaryotic RNA polymerase III.

Authors:  Aneeshkumar G Arimbasseri; Keshab Rijal; Richard J Maraia
Journal:  Biochim Biophys Acta       Date:  2012-10-23
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