Literature DB >> 7553869

Overcoming a nucleosomal barrier to transcription.

V M Studitsky1, D J Clark, G Felsenfeld.   

Abstract

We have studied the kinetics of transcription through a nucleosome core. RNA polymerase transcribes the first approximately 25 bp of nucleosomal DNA rapidly, but then hits a barrier and continues slowly to the nucleosomal dyad region. Here, the barrier disappears and the transcript is completed at a rapid rate, as if on free DNA, indicating that histone octamer transfer is completed as polymerase reaches the dyad. If DNA behind the polymerase is removed during transcription, the barrier does not appear until the polymerase has penetrated up to 15 bp farther into the nucleosome. On a longer template, the barrier is almost eliminated. We have shown previously that the octamer is transferred around the transcribing polymerase via an intermediate containing an intranucleosomal DNA loop. Our results exclude the possibility that polymerase has difficulty breaking histone-DNA contacts and suggest instead that polymerase pauses because it has difficulty transcribing DNA in the loop.

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Year:  1995        PMID: 7553869     DOI: 10.1016/0092-8674(95)90230-9

Source DB:  PubMed          Journal:  Cell        ISSN: 0092-8674            Impact factor:   41.582


  45 in total

1.  Efficiency of expression of transfected genes depends on the cell cycle.

Authors:  S Marenzi; R L Adams; G Zardo; L Lenti; A Reale; P Caiafa
Journal:  Mol Biol Rep       Date:  1999-12       Impact factor: 2.316

2.  Effects of histone tail domains on the rate of transcriptional elongation through a nucleosome.

Authors:  R U Protacio; G Li; P T Lowary; J Widom
Journal:  Mol Cell Biol       Date:  2000-12       Impact factor: 4.272

3.  New insights into unwrapping DNA from the nucleosome from a single-molecule optical tweezers method.

Authors:  Jeffrey J Hayes; Jeffrey C Hansen
Journal:  Proc Natl Acad Sci U S A       Date:  2002-02-19       Impact factor: 11.205

4.  Relationship between retroviral DNA integration and gene expression.

Authors:  J B Weidhaas; E L Angelichio; S Fenner; J M Coffin
Journal:  J Virol       Date:  2000-09       Impact factor: 5.103

5.  Evidence for DNA translocation by the ISWI chromatin-remodeling enzyme.

Authors:  Iestyn Whitehouse; Chris Stockdale; Andrew Flaus; Mark D Szczelkun; Tom Owen-Hughes
Journal:  Mol Cell Biol       Date:  2003-03       Impact factor: 4.272

6.  hSWI/SNF-catalyzed nucleosome sliding does not occur solely via a twist-diffusion mechanism.

Authors:  Sayura Aoyagi; Jeffrey J Hayes
Journal:  Mol Cell Biol       Date:  2002-11       Impact factor: 4.272

7.  Structural Analysis of the Key Intermediate Formed during Transcription through a Nucleosome.

Authors:  H-W Chang; A K Shaytan; F-K Hsieh; O I Kulaeva; M P Kirpichnikov; V M Studitsky
Journal:  Trends Cell Mol Biol       Date:  2013

8.  Functional cooperation between FACT and MCM helicase facilitates initiation of chromatin DNA replication.

Authors:  Bertrand Chin-Ming Tan; Cheng-Ting Chien; Susumu Hirose; Sheng-Chung Lee
Journal:  EMBO J       Date:  2006-08-10       Impact factor: 11.598

9.  The nucleosome: a transparent, slippery, sticky and yet stable DNA-protein complex.

Authors:  H Schiessel
Journal:  Eur Phys J E Soft Matter       Date:  2006-02-02       Impact factor: 1.890

10.  Nucleosome binding by the polymerase I transactivator upstream binding factor displaces linker histone H1.

Authors:  M Kermekchiev; J L Workman; C S Pikaard
Journal:  Mol Cell Biol       Date:  1997-10       Impact factor: 4.272

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