Literature DB >> 11435570

Polymerase slippage at vesicular stomatitis virus gene junctions to generate poly(A) is regulated by the upstream 3'-AUAC-5' tetranucleotide: implications for the mechanism of transcription termination.

J N Barr1, G W Wertz.   

Abstract

Termination of mRNA synthesis in vesicular stomatitis virus (VSV), the prototypic rhabdovirus, is controlled by a 13-nucleotide gene end sequence which comprises the conserved tetranucleotide 3'-AUAC-5', the U(7) tract and the intergenic dinucleotide. mRNAs terminated at this sequence possess 100- to 300-nucleotide-long 3' poly(A) tails which are thought to result from polymerase slippage (reiterative transcription) by the VSV polymerase on the U(7) tract. Previously we determined that in addition to the AUAC tetranucleotide, the U(7) tract was an essential signal in the termination process. Shortening or interrupting the U(7) tract abolished termination. These altered U tracts also prevented the polymerase from performing reiterative transcription necessary for generation of the mRNA poly(A) tail and thus established seven residues as the minimum length of U tract that allowed reiterative transcription to occur. In this study we investigated whether sequences other than the essential U(7) tract are involved in controlling polymerase slippage. We investigated whether the AUAC tetranucleotide affected the process of reiterative transcription by analyzing the nucleotide sequence of RNAs transcribed from altered subgenomic templates and infectious VSV variants. The tetranucleotide was found to regulate reiterative transcription on the U(7) tract. The extent of polymerase slippage was governed not by specific tetranucleotide sequences but rather by nucleotide composition such that slippage occurred when the tetranucleotide was composed of A or U residues but not when it was composed of G or C residues. This suggested that polymerase slippage was controlled, at least in part, by the strength of base pairing between the template and nascent strands. Further data presented here indicate that the tetranucleotide contains both a signal that directs the VSV polymerase to slip on the downstream U(7) tract and also a signal that directs a slipping polymerase to terminate mRNA synthesis.

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Year:  2001        PMID: 11435570      PMCID: PMC114418          DOI: 10.1128/JVI.75.15.6901-6913.2001

Source DB:  PubMed          Journal:  J Virol        ISSN: 0022-538X            Impact factor:   5.103


  42 in total

1.  Complete nucleotide sequence of the leader RNA synthesized in vitro by vesicular stomatitis virus.

Authors:  R J Colonno; A K Banerjee
Journal:  Cell       Date:  1978-09       Impact factor: 41.582

2.  Sequential transcription of the genes of vesicular stomatitis virus.

Authors:  G Abraham; A K Banerjee
Journal:  Proc Natl Acad Sci U S A       Date:  1976-05       Impact factor: 11.205

3.  Intervening polyadenylate sequences in RNA transcripts of vesicular stomatitis virus.

Authors:  R C Herman; S Adler; R A Lazzarini; R J Colonno; A K Banerjee; H Westphal
Journal:  Cell       Date:  1978-10       Impact factor: 41.582

4.  GP mRNA of Ebola virus is edited by the Ebola virus polymerase and by T7 and vaccinia virus polymerases.

Authors:  V E Volchkov; S Becker; V A Volchkova; V A Ternovoj; A N Kotov; S V Netesov; H D Klenk
Journal:  Virology       Date:  1995-12-20       Impact factor: 3.616

5.  Structure of the gene N:gene NS intercistronic junction in the genome of vesicular stomatitis virus.

Authors:  D J McGeoch
Journal:  Cell       Date:  1979-07       Impact factor: 41.582

6.  Order of transcription of genes of vesicular stomatitis virus.

Authors:  L A Ball; C N White
Journal:  Proc Natl Acad Sci U S A       Date:  1976-02       Impact factor: 11.205

7.  Determination of molar ratios of vesicular stomatitis virus induced RNA species in BHK21 cells.

Authors:  L P Villarreal; M Breindl; J J Holland
Journal:  Biochemistry       Date:  1976-04-20       Impact factor: 3.162

8.  Identification of a minimal size requirement for termination of vesicular stomatitis virus mRNA: implications for the mechanism of transcription.

Authors:  S P Whelan; J N Barr; G W Wertz
Journal:  J Virol       Date:  2000-09       Impact factor: 5.103

9.  A unique RNA species involved in initiation of vesicular stomatitis virus RNA transcription in vitro.

Authors:  R J Colonno; A K Banerjee
Journal:  Cell       Date:  1976-06       Impact factor: 41.582

10.  Giant heterogeneous polyadenylic acid on vesicular stomatitis virus mRNA synthesized in vitro in the presence of S-adenosylhomocysteine.

Authors:  J K Rose; H F Lodish; M L Brock
Journal:  J Virol       Date:  1977-02       Impact factor: 5.103

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  37 in total

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Authors:  Gail W Wertz; Robin Moudy; L Andrew Ball
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2.  Transcription and replication initiate at separate sites on the vesicular stomatitis virus genome.

Authors:  Sean P J Whelan; Gail W Wertz
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3.  A transcriptionally active subgenomic promoter supports homologous crossovers in a plus-strand RNA virus.

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4.  Efficient in vitro system of homologous recombination in brome mosaic bromovirus.

Authors:  Rafal Wierzchoslawski; Jozef J Bujarski
Journal:  J Virol       Date:  2006-06       Impact factor: 5.103

5.  Second-site mutations selected in transcriptional regulatory sequences compensate for engineered mutations in the vesicular stomatitis virus nucleocapsid protein.

Authors:  Djamila Harouaka; Gail W Wertz
Journal:  J Virol       Date:  2012-08-08       Impact factor: 5.103

6.  Opposing effects of inhibiting cap addition and cap methylation on polyadenylation during vesicular stomatitis virus mRNA synthesis.

Authors:  Jianrong Li; Amal Rahmeh; Vesna Brusic; Sean P J Whelan
Journal:  J Virol       Date:  2008-12-10       Impact factor: 5.103

7.  Attenuation control of pyrG expression in Bacillus subtilis is mediated by CTP-sensitive reiterative transcription.

Authors:  Qi Meng; Charles L Turnbough; Robert L Switzer
Journal:  Proc Natl Acad Sci U S A       Date:  2004-07-13       Impact factor: 11.205

8.  S-adenosyl homocysteine-induced hyperpolyadenylation of vesicular stomatitis virus mRNA requires the methyltransferase activity of L protein.

Authors:  Summer E Galloway; Gail W Wertz
Journal:  J Virol       Date:  2008-10-01       Impact factor: 5.103

9.  Molecular characterization of the Great Lakes viral hemorrhagic septicemia virus (VHSV) isolate from USA.

Authors:  Arun Ammayappan; Vikram N Vakharia
Journal:  Virol J       Date:  2009-10-25       Impact factor: 4.099

10.  Molecular characterization of the virulent infectious hematopoietic necrosis virus (IHNV) strain 220-90.

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