Literature DB >> 7836462

RNA polymerase II ternary complexes may become arrested after transcribing to within 10 bases of the end of linear templates.

M G Izban1, I Samkurashvili, D S Luse.   

Abstract

In the presence of elongation factor SII, arrested RNA polymerase II ternary complexes cleave 7-17 nucleotides from the 3'-ends of their nascent RNAs. It has been shown that transcription of linear templates generates apparent run-off RNAs, which are nevertheless truncated upon incubation with SII. By using high resolution gels, we demonstrate that transcription of blunt or 3'-overhung templates with RNA polymerase II generates two populations of ternary complexes. The first class pauses 5-10 bases prior to the end of the template strand. These complexes respond to SII by cleaving approximately 9-17 nucleotide RNAs from their 3'-ends and therefore may be termed arrested. A second class of complexes, which fail to respond to SII, transcribe to within 3 bases of the end of the template strand. These complexes appear to have run off the template since they have released their nascent RNAs. Run-off transcription occurs on all types of templates, but it is the predominant reaction on DNAs with 5'-overhung ends. Thus, RNA polymerase II ternary complexes that retain 5-10 bases of contact with the template strand down-stream of the catalytic site become arrested. Further reduction of downstream template contacts can lead to termination. We also show that the addition of Sarkosyl to the elongation reactions significantly changes the pattern of transcriptional arrest near the end of linear templates.

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Year:  1995        PMID: 7836462     DOI: 10.1074/jbc.270.5.2290

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  12 in total

1.  Strong natural pausing by RNA polymerase II within 10 bases of transcription start may result in repeated slippage and reextension of the nascent RNA.

Authors:  Mahadeb Pal; Donal S Luse
Journal:  Mol Cell Biol       Date:  2002-01       Impact factor: 4.272

2.  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

Review 3.  RNA polymerase II transcription elongation control.

Authors:  Jiannan Guo; David H Price
Journal:  Chem Rev       Date:  2013-08-06       Impact factor: 60.622

4.  A novel RNA polymerase I-dependent RNase activity that shortens nascent transcripts from the 3' end.

Authors:  H Tschochner
Journal:  Proc Natl Acad Sci U S A       Date:  1996-11-12       Impact factor: 11.205

5.  Template topology and transcription: chromatin templates relaxed by localized linearization are transcriptionally active in yeast.

Authors:  C P Liang; W T Garrard
Journal:  Mol Cell Biol       Date:  1997-05       Impact factor: 4.272

6.  Flipping states: a few key residues decide the winning conformation of the only universally conserved transcription factor.

Authors:  Da Shi; Dmitri Svetlov; Ruben Abagyan; Irina Artsimovitch
Journal:  Nucleic Acids Res       Date:  2017-09-06       Impact factor: 16.971

7.  Escherichia coli RNA polymerase terminates transcription efficiently at rho-independent terminators on single-stranded DNA templates.

Authors:  S M Uptain; M J Chamberlin
Journal:  Proc Natl Acad Sci U S A       Date:  1997-12-09       Impact factor: 11.205

8.  The Nun protein of bacteriophage HK022 inhibits translocation of Escherichia coli RNA polymerase without abolishing its catalytic activities.

Authors:  S C Hung; M E Gottesman
Journal:  Genes Dev       Date:  1997-10-15       Impact factor: 11.361

9.  A model in vitro system for co-transcriptional splicing.

Authors:  Yong Yu; Rita Das; Eric G Folco; Robin Reed
Journal:  Nucleic Acids Res       Date:  2010-07-14       Impact factor: 16.971

10.  Variation in the size of nascent RNA cleavage products as a function of transcript length and elongation competence.

Authors:  W Gu; D Reines
Journal:  J Biol Chem       Date:  1995-12-22       Impact factor: 5.157

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