High-frequency leader sequence switching during coronavirus defective interfering RNA replication.
about
Cooperation of an RNA packaging signal and a viral envelope protein in coronavirus RNA packagingA recombinant hepatitis C virus RNA-dependent RNA polymerase capable of copying the full-length viral RNA.Importance of the positive-strand RNA secondary structure of a murine coronavirus defective interfering RNA internal replication signal in positive-strand RNA synthesis.Coronavirus transcription early in infectionDownstream sequences influence the choice between a naturally occurring noncanonical and closely positioned upstream canonical heptameric fusion motif during bovine coronavirus subgenomic mRNA synthesis.An in vitro system for the leader-primed transcription of coronavirus mRNAsStem-loop IV in the 5' untranslated region is a cis-acting element in bovine coronavirus defective interfering RNA replicationBovine coronavirus 5'-proximal genomic acceptor hotspot for discontinuous transcription is 65 nucleotides wide.Heterogeneous nuclear ribonucleoprotein A1 regulates RNA synthesis of a cytoplasmic virusAn optimal cis-replication stem-loop IV in the 5' untranslated region of the mouse coronavirus genome extends 16 nucleotides into open reading frame 1.A leaderless genome identified during persistent bovine coronavirus infection is associated with attenuation of gene expression.5'-proximal hot spot for an inducible positive-to-negative-strand template switch by coronavirus RNA-dependent RNA polymerase.The effect of two closely inserted transcription consensus sequences on coronavirus transcription.Two murine coronavirus genes suffice for viral RNA synthesis.Characterization of a murine coronavirus defective interfering RNA internal cis-acting replication signal.A 5'-proximal RNA sequence of murine coronavirus as a potential initiation site for genomic-length mRNA transcriptionThe UCUAAAC promoter motif is not required for high-frequency leader recombination in bovine coronavirus defective interfering RNAReplication of murine coronavirus defective interfering RNA from negative-strand transcripts.An RNA stem-loop within the bovine coronavirus nsp1 coding region is a cis-acting element in defective interfering RNA replication.A novel 3'-end repair mechanism in an RNA virus.Requirement of the 5'-end genomic sequence as an upstream cis-acting element for coronavirus subgenomic mRNA transcription.Coronavirus leader RNA regulates and initiates subgenomic mRNA transcription both in trans and in cis.Evidence for coronavirus discontinuous transcription.Unusual heterogeneity of leader-mRNA fusion in a murine coronavirus: implications for the mechanism of RNA transcription and recombination.Genetics of mouse hepatitis virus transcription: evidence that subgenomic negative strands are functional templates.A cis-acting function for the coronavirus leader in defective interfering RNA replication.Effect of intergenic consensus sequence flanking sequences on coronavirus transcriptionMutagenic analysis of the coronavirus intergenic consensus sequence.Mechanism of coronavirus transcription: duration of primary transcription initiation activity and effects of subgenomic RNA transcription on RNA replication.Identification and characterization of a coronavirus packaging signalCoronavirus mRNA transcription: UV light transcriptional mapping studies suggest an early requirement for a genomic-length templateRNA recombination in a coronavirus: recombination between viral genomic RNA and transfected RNA fragments.A translation-attenuating intraleader open reading frame is selected on coronavirus mRNAs during persistent infection.Bovine coronavirus mRNA replication continues throughout persistent infection in cell culture.Analysis of efficiently packaged defective interfering RNAs of murine coronavirus: localization of a possible RNA-packaging signalA system for study of coronavirus mRNA synthesis: a regulated, expressed subgenomic defective interfering RNA results from intergenic site insertion.The leader RNA of coronavirus mouse hepatitis virus contains an enhancer-like element for subgenomic mRNA transcription.Translation but not the encoded sequence is essential for the efficient propagation of the defective interfering RNAs of the coronavirus mouse hepatitis virusThe function of the spike protein of mouse hepatitis virus strain A59 can be studied on virus-like particles: cleavage is not required for infectivity.Three different cellular proteins bind to complementary sites on the 5'-end-positive and 3'-end-negative strands of mouse hepatitis virus RNA.
P2860
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P2860
High-frequency leader sequence switching during coronavirus defective interfering RNA replication.
description
1989 nî lūn-bûn
@nan
1989年の論文
@ja
1989年論文
@yue
1989年論文
@zh-hant
1989年論文
@zh-hk
1989年論文
@zh-mo
1989年論文
@zh-tw
1989年论文
@wuu
1989年论文
@zh
1989年论文
@zh-cn
name
High-frequency leader sequence ...... e interfering RNA replication.
@en
type
label
High-frequency leader sequence ...... e interfering RNA replication.
@en
prefLabel
High-frequency leader sequence ...... e interfering RNA replication.
@en
P2860
P1433
P1476
High-frequency leader sequence ...... e interfering RNA replication.
@en
P2093
P2860
P304
P407
P577
1989-12-01T00:00:00Z