Transcription and replication initiate at separate sites on the vesicular stomatitis virus genome - Wikidata - wikimedia - TriplyDB

Transcription and replication initiate at separate sites on the vesicular stomatitis virus genome

Transcription and replication initiate at separate sites on the vesicular stomatitis virus genome

http://www.wikidata.org/entity/Q34034236

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Initiation and regulation of paramyxovirus transcription and replication Protein expression redirects vesicular stomatitis virus RNA synthesis to cytoplasmic inclusions Vesicular Stomatitis Virus mRNA Capping Machinery Requires Specific cis-Acting Signals in the RNA Ribose 2'-O Methylation of the Vesicular Stomatitis Virus mRNA Cap Precedes and Facilitates Subsequent Guanine-N-7 Methylation by the Large Polymerase Protein Interferon-γ Inhibits Ebola Virus Infection Second-site mutations selected in transcriptional regulatory sequences compensate for engineered mutations in the vesicular stomatitis virus nucleocapsid protein Importance of hydrogen bond contacts between the N protein and RNA genome of vesicular stomatitis virus in encapsidation and RNA synthesis A temperature sensitive VSV identifies L protein residues that affect transcription but not replication.Mutations in the C-terminal loop of the nucleocapsid protein affect vesicular stomatitis virus RNA replication and transcription differentially.Identification of internal sequences in the 3' leader region of human respiratory syncytial virus that enhance transcription and confer replication processivity.A freeze frame view of vesicular stomatitis virus transcription defines a minimal length of RNA for 5' processing Amino acid residues within conserved domain VI of the vesicular stomatitis virus large polymerase protein essential for mRNA cap methyltransferase activity Crystal structure of the oligomerization domain of the phosphoprotein of vesicular stomatitis virus A unique strategy for mRNA cap methylation used by vesicular stomatitis virus.Vesicular stomatitis virus polymerase's strong affinity to its template suggests exotic transcription models.Cell-type-specific growth restriction of vesicular stomatitis virus polR mutants is linked to defective viral polymerase function.Vesicular stomatitis viruses resistant to the methylase inhibitor sinefungin upregulate RNA synthesis and reveal mutations that affect mRNA cap methylation Respiratory syncytial virus polymerase can initiate transcription from position 3 of the leader promoter Viral transgenesis of embryonic cell cultures from the freshwater microcrustacean Daphnia.Mutational analysis reveals a noncontractile but interactive role of actin and profilin in viral RNA-dependent RNA synthesis.mRNA cap methylation influences pathogenesis of vesicular stomatitis virus in vivo.Two RNA polymerase complexes from vesicular stomatitis virus-infected cells that carry out transcription and replication of genome RNA.The nucleocapsid of vesicular stomatitis virus.Genetic inactivation of COPI coatomer separately inhibits vesicular stomatitis virus entry and gene expression.Dissociation of rabies virus matrix protein functions in regulation of viral RNA synthesis and virus assembly.Structure of the L Protein of Vesicular Stomatitis Virus from Electron Cryomicroscopy.Opposing effects of inhibiting cap addition and cap methylation on polyadenylation during vesicular stomatitis virus mRNA synthesis.Roles of human parainfluenza virus type 3 bases 13 to 78 in replication and transcription: identification of an additional replication promoter element and evidence for internal transcription initiation.A conserved motif in region v of the large polymerase proteins of nonsegmented negative-sense RNA viruses that is essential for mRNA capping.Asymmetric packaging of polymerases within vesicular stomatitis virus.Structural properties of the C terminus of vesicular stomatitis virus N protein dictate N-RNA complex assembly, encapsidation, and RNA synthesis.Mechanism of RNA synthesis initiation by the vesicular stomatitis virus polymerase.Evidence that the respiratory syncytial virus polymerase is recruited to nucleotides 1 to 11 at the 3' end of the nucleocapsid and can scan to access internal signals.The glutamic residue at position 402 in the C-terminus of Newcastle disease virus nucleoprotein is critical for the virus.

P2860

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P2860

Transcription and replication initiate at separate sites on the vesicular stomatitis virus genome

http://www.wikidata.org/entity/Q34034236

description

2002 nî lūn-bûn

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2002 թուականի Յունիսին հրատարակուած գիտական յօդուած

@hyw

2002 թվականի հունիսին հրատարակված գիտական հոդված

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2002年の論文

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2002年学术文章

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2002年学术文章

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2002年学术文章

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2002年学术文章

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2002年学术文章

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2002年學術文章

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name

Transcription and replication ...... icular stomatitis virus genome

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Transcription and replication ...... icular stomatitis virus genome

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Transcription and replication ...... icular stomatitis virus genome

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Transcription and replication ...... icular stomatitis virus genome

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Transcription and replication ...... icular stomatitis virus genome

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Transcription and replication ...... icular stomatitis virus genome

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Transcription and replication ...... icular stomatitis virus genome

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Transcription and replication ...... icular stomatitis virus genome

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Transcription and replication ...... icular stomatitis virus genome

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P1433

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Proceedings of the National Academy of Sciences of the United States of America

P1476

Transcription and replication ...... icular stomatitis virus genome

@en

P2093

Gail W Wertz

http://www.w3.org/2001/XMLSchema#string

Sean P J Whelan

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P2860

RNA- temperature-sensitive mutants of vesicular stomatitis virus: L-protein thermosensitivity accounts for transcriptase restriction of group I mutants.

Both NS and L proteins are required for in vitro RNA synthesis by vesicular stomatitis virus

Dissociation and reconstitution of the transcriptase and template activities of vesicular stomatitis B and T virions.

In vitro synthesis of triphosphate-initiated N-gene mRNA oligonucleotides is regulated by the matrix protein of vesicular stomatitis virus

The 5' terminal trailer region of vesicular stomatitis virus contains a position-dependent cis-acting signal for assembly of RNA into infectious particles.

Overlapping signals for transcription and replication at the 3' terminus of the vesicular stomatitis virus genome.

Transcript initiation and 5'-end modifications are separable events during vesicular stomatitis virus transcription.

Ribonucleic acid synthesis of vesicular stomatitis virus, II. An RNA polymerase in the virion.

Polyadenylation of vesicular stomatitis virus mRNA dictates efficient transcription termination at the intercistronic gene junctions.

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.

P304

9178-9183

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scholarly article

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10.1073/PNAS.152155599

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14

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99

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2002-06-27T00:00:00Z

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11286882

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12089339

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123114

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