Literature DB >> 18433825

Determinants of vaccinia virus early gene transcription termination.

Sarah Piacente1, Linda Christen, Benjamin Dickerman, Mohamed R Mohamed, Edward G Niles.   

Abstract

Vaccinia virus early gene transcription requires the vaccinia termination factor, VTF, nucleoside triphosphate phosphohydrolase I, NPH I, ATP, the virion RNA polymerase, and the motif, UUUUUNU, in the nascent RNA, found within 30 to 50 bases from the poly A addition site, in vivo. In this study, the relationships among the vaccinia early gene transcription termination efficiency, termination motif specificity, and the elongation rate were investigated. A low transcription elongation rate maximizes termination efficiency and minimizes specificity for the UUUUUNU motif. Positioning the termination motif over a 63 base area upstream from the RNA polymerase allowed efficient transcript release, demonstrating a remarkable plasticity in the transcription termination complex. Efficient transcript release was observed during ongoing transcription, independent of VTF or UUUUUNU, but requiring both NPH I and either ATP or dATP. This argues for a two step model: the specifying step, requiring both VTF and UUUUUNU, and the energy-dependent step employing NPH I and ATP. Evaluation of NPH I mutants for the ability to stimulate transcription elongation demonstrated that ATPase activity and a stable interaction between NPH I and the Rap94 subunit of the viral RNA polymerase are required. These observations demonstrate that NPH I is a component of the elongating RNA polymerase, which is catalytically active during transcription elongation.

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Year:  2008        PMID: 18433825      PMCID: PMC2483243          DOI: 10.1016/j.virol.2008.03.011

Source DB:  PubMed          Journal:  Virology        ISSN: 0042-6822            Impact factor:   3.616


  45 in total

1.  Interaction between nucleoside triphosphate phosphohydrolase I and the H4L subunit of the viral RNA polymerase is required for vaccinia virus early gene transcript release.

Authors:  M R Mohamed; E G Niles
Journal:  J Biol Chem       Date:  2000-08-18       Impact factor: 5.157

2.  Antibodies directed against an epitope in the N-terminal region of the H4L subunit of the vaccinia virus RNA polymerase inhibit both transcription initiation and transcription termination, in vitro.

Authors:  Mohamed R Mohamed; Linda A Christen; Edward G Niles
Journal:  Virology       Date:  2002-07-20       Impact factor: 3.616

3.  Two nucleic acid-dependent nucleoside triphosphate phosphohydrolases from vaccinia virus. Nucleotide substrate and polynucleotide cofactor specificities.

Authors:  E Paoletti; B Moss
Journal:  J Biol Chem       Date:  1974-05-25       Impact factor: 5.157

Review 4.  Vaccinia virus transcription.

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

5.  Oligonucleotide sequence signaling transcriptional termination of vaccinia virus early genes.

Authors:  L Yuen; B Moss
Journal:  Proc Natl Acad Sci U S A       Date:  1987-09       Impact factor: 11.205

6.  Effect of selected mutations in the C-terminal region of the vaccinia virus nucleoside triphosphate phosphohydrolase I on binding to the H4L subunit of the viral RNA polymerase and early gene transcription termination in vitro.

Authors:  Sarah C Piacente; Linda A Christen; Mohamed Ragaa Mohamed; Edward G Niles
Journal:  Virology       Date:  2003-05-25       Impact factor: 3.616

7.  UUUUUNU stimulation of vaccinia virus early gene transcription termination. Oligonucleotide sequence and structural requirements for stimulation of premature termination in vitro.

Authors:  Mohamed Ragaa Mohamed; Edward G Niles
Journal:  J Biol Chem       Date:  2003-07-30       Impact factor: 5.157

8.  UUUUUNU oligonucleotide stimulation of vaccinia virus early gene transcription termination, in trans.

Authors:  Mohamed Ragaa Mohamed; Edward G Niles
Journal:  J Biol Chem       Date:  2003-01-28       Impact factor: 5.157

9.  Modification of the 5'-terminus of mRNA by soluble guanylyl and methyl transferases from vaccinia virus.

Authors:  M J Ensinger; S A Martin; E Paoletti; B Moss
Journal:  Proc Natl Acad Sci U S A       Date:  1975-07       Impact factor: 11.205

10.  An isatin-beta-thiosemicarbazone-resistant vaccinia virus containing a mutation in the second largest subunit of the viral RNA polymerase is defective in transcription elongation.

Authors:  Cindy Prins; Steven G Cresawn; Richard C Condit
Journal:  J Biol Chem       Date:  2004-08-03       Impact factor: 5.157

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  4 in total

1.  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

Review 2.  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

3.  The NPH-II helicase displays efficient DNA x RNA helicase activity and a pronounced purine sequence bias.

Authors:  Sean David Taylor; Amanda Solem; Jane Kawaoka; Anna Marie Pyle
Journal:  J Biol Chem       Date:  2010-01-28       Impact factor: 5.157

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

Authors:  Ryan Hindman; Paul Gollnick
Journal:  J Biol Chem       Date:  2016-05-06       Impact factor: 5.157

  4 in total

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