Literature DB >> 27189950

Nucleoside Triphosphate Phosphohydrolase I (NPH I) Functions as a 5' to 3' Translocase in Transcription Termination of Vaccinia Early Genes.

Ryan Hindman1, Paul Gollnick2.   

Abstract

Vaccinia virus early genes are transcribed immediately upon infection. Nucleoside triphosphate phosphohydrolase I (NPH I) is an essential component of the early gene transcription complex. NPH I hydrolyzes ATP to release transcripts during transcription termination. The ATPase activity of NPH I requires single-stranded (ss) DNA as a cofactor; however, the source of this cofactor within the transcription complex is not known. Based on available structures of transcription complexes it has been hypothesized that the ssDNA cofactor is obtained from the unpaired non-template strand within the transcription bubble. In vitro transcription on templates that lack portions of the non-template strand within the transcription bubble showed that the upstream portion of the transcription bubble is required for efficient NPH I-mediated transcript release. Complementarity between the template and non-template strands in this region is also required for NPH I-mediated transcript release. This observation complicates locating the source of the ssDNA cofactor within the transcription complex because removal of the non-template strand also disrupts transcription bubble reannealing. Prior studies have shown that ssRNA binds to NPH I, but it does not activate ATPase activity. Chimeric transcription templates with RNA in the non-template strand confirm that the source of the ssDNA cofactor for NPH I is the upstream portion of the non-template strand in the transcription bubble. Consistent with this conclusion we also show that isolated NPH I acts as a 5' to 3' translocase on single-stranded DNA.
© 2016 by The American Society for Biochemistry and Molecular Biology, Inc.

Entities:  

Keywords:  ATPase; transcription; transcription termination; viral polymerase; viral transcription

Mesh:

Substances:

Year:  2016        PMID: 27189950      PMCID: PMC4938199          DOI: 10.1074/jbc.M116.730135

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


  61 in total

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

Authors:  Thomas J Santangelo; Jeffrey W Roberts
Journal:  Mol Cell       Date:  2004-04-09       Impact factor: 17.970

2.  Vaccinia NPH-I, a DExH-box ATPase, is the energy coupling factor for mRNA transcription termination.

Authors:  L Deng; S Shuman
Journal:  Genes Dev       Date:  1998-02-15       Impact factor: 11.361

3.  Crystal Structure of a Transcribing RNA Polymerase II Complex Reveals a Complete Transcription Bubble.

Authors:  Christopher O Barnes; Monica Calero; Indranil Malik; Brian W Graham; Henrik Spahr; Guowu Lin; Aina E Cohen; Ian S Brown; Qiangmin Zhang; Filippo Pullara; Michael A Trakselis; Craig D Kaplan; Guillermo Calero
Journal:  Mol Cell       Date:  2015-07-16       Impact factor: 17.970

4.  The D1 and D12 subunits are both essential for the transcription termination factor activity of vaccinia virus capping enzyme.

Authors:  Y Luo; X Mao; L Deng; P Cong; S Shuman
Journal:  J Virol       Date:  1995-06       Impact factor: 5.103

5.  Biotin-streptavidin-labeled oligonucleotides as probes of helicase mechanisms.

Authors:  P D Morris; A J Tackett; K D Raney
Journal:  Methods       Date:  2001-02       Impact factor: 3.608

Review 6.  Vaccinia virus transcription.

Authors:  Steven S Broyles
Journal:  J Gen Virol       Date:  2003-09       Impact factor: 3.891

7.  Vaccinia virus nucleoside triphosphate phosphohydrolase I controls early and late gene expression by regulating the rate of transcription.

Authors:  M Diaz-Guerra; M Esteban
Journal:  J Virol       Date:  1993-12       Impact factor: 5.103

8.  Determinants of vaccinia virus early gene transcription termination.

Authors:  Sarah Piacente; Linda Christen; Benjamin Dickerman; Mohamed R Mohamed; Edward G Niles
Journal:  Virology       Date:  2008-04-22       Impact factor: 3.616

9.  The vaccinia virus A18R gene product is a DNA-dependent ATPase.

Authors:  C D Bayliss; R C Condit
Journal:  J Biol Chem       Date:  1995-01-27       Impact factor: 5.157

10.  Investigation of translocation, DNA unwinding, and protein displacement by NS3h, the helicase domain from the hepatitis C virus helicase.

Authors:  Dennis L Matlock; Laxmi Yeruva; Alicia K Byrd; Samuel G Mackintosh; Clint Langston; Carrie Brown; Craig E Cameron; Christopher J Fischer; Kevin D Raney
Journal:  Biochemistry       Date:  2010-03-16       Impact factor: 3.162

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