Sendai virus genome synthesis and assembly are coupled: a possible mechanism to promote viral RNA polymerase processivity.
about
Sendai virus trailer RNA binds TIAR, a cellular protein involved in virus-induced apoptosisInitiation and regulation of paramyxovirus transcription and replicationStructural Insight into Nucleoprotein Conformation Change Chaperoned by VP35 peptide in Marburg virus.Identification of internal sequences in the 3' leader region of human respiratory syncytial virus that enhance transcription and confer replication processivity.Evidence that the polymerase of respiratory syncytial virus initiates RNA replication in a nontemplated fashion.Chemical modification of nucleotide bases and mRNA editing depend on hexamer or nucleoprotein phase in Sendai virus nucleocapsids.Ambisense sendai viruses are inherently unstable but are useful to study viral RNA synthesis.The first two nucleotides of the respiratory syncytial virus antigenome RNA replication product can be selected independently of the promoter terminusCompetition between the Sendai virus N mRNA start site and the genome 3'-end promoter for viral RNA polymeraseRespiratory syncytial virus polymerase can initiate transcription from position 3 of the leader promoterSendai virus C protein plays a role in restricting PKR activation by limiting the generation of intracellular double-stranded RNA.Polymerases of paramyxoviruses and pneumoviruses.Failure to activate the IFN-β promoter by a paramyxovirus lacking an interferon antagonist.Restriction of measles virus RNA synthesis by a mouse host cell line: trans-complementation by polymerase components or a human cellular factor(s)Non-encapsidated 5' copy-back defective-interfering genomes produced by recombinant measles viruses are recognized by RIG-I and LGP2 but not MDA5.Dissociation of rabies virus matrix protein functions in regulation of viral RNA synthesis and virus assembly.Dynamics of viral RNA synthesis during measles virus infection.Self-Assembly of Measles Virus Nucleocapsid-like Particles: Kinetics and RNA Sequence Dependence.Respiratory Syncytial Virus Inhibitor AZ-27 Differentially Inhibits Different Polymerase Activities at the PromoterIdentification of RNA partners of viral proteins in infected cells.Investigating the specificity and stoichiometry of RNA binding by the nucleocapsid protein of Bunyamwera virus.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.Persistent and stable gene expression by a cytoplasmic RNA replicon based on a noncytopathic variant Sendai virus.RNA elongation by respiratory syncytial virus polymerase is calibrated by conserved region V.The control of paramyxovirus genome hexamer length and mRNA editing.
P2860
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P2860
Sendai virus genome synthesis and assembly are coupled: a possible mechanism to promote viral RNA polymerase processivity.
description
2001 nî lūn-bûn
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2001年の論文
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2001年学术文章
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2001年学术文章
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2001年学术文章
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name
Sendai virus genome synthesis ...... l RNA polymerase processivity.
@en
Sendai virus genome synthesis ...... l RNA polymerase processivity.
@nl
type
label
Sendai virus genome synthesis ...... l RNA polymerase processivity.
@en
Sendai virus genome synthesis ...... l RNA polymerase processivity.
@nl
prefLabel
Sendai virus genome synthesis ...... l RNA polymerase processivity.
@en
Sendai virus genome synthesis ...... l RNA polymerase processivity.
@nl
P2093
P1476
Sendai virus genome synthesis ...... l RNA polymerase processivity.
@en
P2093
P304
P356
10.1099/0022-1317-82-12-2895
P407
P577
2001-12-01T00:00:00Z