Literature DB >> 8047884

Discontinuous mechanism of transcription elongation.

E Nudler1, A Goldfarb, M Kashlev.   

Abstract

During transcription elongation, three flexibly connected parts of RNA polymerase of Escherichia coli advance along the template so that the front-end domain is followed by the catalytic site which in turn is followed by the RNA product binding site. The advancing enzyme was found to maintain the same conformation throughout extended segments of the transcribed region. However, when the polymerase traveled across certain DNA sites that seemed to briefly anchor the front-end domain, cyclic shifting of the three parts, accompanied by buildup and relief of internal strain, was observed. Thus, elongation proceeded in alternating laps of monotonous and inchworm-like movement with the flexible RNA polymerase configuration being subject to direct sequence control.

Entities:  

Mesh:

Substances:

Year:  1994        PMID: 8047884     DOI: 10.1126/science.8047884

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  59 in total

1.  Structural characterization of RNA polymerase II complexes arrested by a cyclobutane pyrimidine dimer in the transcribed strand of template DNA.

Authors:  S Tornaletti; D Reines; P C Hanawalt
Journal:  J Biol Chem       Date:  1999-08-20       Impact factor: 5.157

2.  Direct observation of one-dimensional diffusion and transcription by Escherichia coli RNA polymerase.

Authors:  M Guthold; X Zhu; C Rivetti; G Yang; N H Thomson; S Kasas; H G Hansma; B Smith; P K Hansma; C Bustamante
Journal:  Biophys J       Date:  1999-10       Impact factor: 4.033

3.  Translocation after synthesis of a four-nucleotide RNA commits RNA polymerase II to promoter escape.

Authors:  Jennifer F Kugel; James A Goodrich
Journal:  Mol Cell Biol       Date:  2002-02       Impact factor: 4.272

4.  Analysis of the open region of RNA polymerase II transcription complexes in the early phase of elongation.

Authors:  U Fiedler; H T Timmers
Journal:  Nucleic Acids Res       Date:  2001-07-01       Impact factor: 16.971

5.  Promoter clearance by RNA polymerase II is an extended, multistep process strongly affected by sequence.

Authors:  M Pal; D McKean; D S Luse
Journal:  Mol Cell Biol       Date:  2001-09       Impact factor: 4.272

6.  TFIIS enhances transcriptional elongation through an artificial arrest site in vivo.

Authors:  D Kulish; K Struhl
Journal:  Mol Cell Biol       Date:  2001-07       Impact factor: 4.272

7.  The initiation-elongation transition: lateral mobility of RNA in RNA polymerase II complexes is greatly reduced at +8/+9 and absent by +23.

Authors:  Mahadeb Pal; Donal S Luse
Journal:  Proc Natl Acad Sci U S A       Date:  2003-04-28       Impact factor: 11.205

8.  Influence of DNA template choice on transcription and inhibition of Escherichia coli RNA polymerase.

Authors:  Joerg Haupenthal; Kristina Hüsecken; Matthias Negri; Christine K Maurer; Rolf W Hartmann
Journal:  Antimicrob Agents Chemother       Date:  2012-06-04       Impact factor: 5.191

9.  Oligonucleotides complementary to the Oxytricha nova telomerase RNA delineate the template domain and uncover a novel mode of primer utilization.

Authors:  M Melek; B T Davis; D E Shippen
Journal:  Mol Cell Biol       Date:  1994-12       Impact factor: 4.272

10.  Repurposing CRISPR as an RNA-guided platform for sequence-specific control of gene expression.

Authors:  Lei S Qi; Matthew H Larson; Luke A Gilbert; Jennifer A Doudna; Jonathan S Weissman; Adam P Arkin; Wendell A Lim
Journal:  Cell       Date:  2013-02-28       Impact factor: 41.582

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.