Mechanism of ribosome recruitment by hepatitis C IRES RNA - Test2 - elhamkhani - TriplyDB

Mechanism of ribosome recruitment by hepatitis C IRES RNA

Mechanism of ribosome recruitment by hepatitis C IRES RNA

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MicroRNA-122 dependent binding of Ago2 protein to hepatitis C virus RNA is associated with enhanced RNA stability and translation stimulation Mass spectrometric analysis of the human 40S ribosomal subunit: native and HCV IRES-bound complexes The DEAD-box helicase DDX3 supports the assembly of functional 80S ribosomes Mass spectrometry reveals modularity and a complete subunit interaction map of the eukaryotic translation factor eIF3 Domains on the hepatitis C virus internal ribosome entry site for 40s subunit binding Alpha interferon induces distinct translational control programs to suppress hepatitis C virus RNA replication Regulation of hepatitis C virus translation and infectious virus production by the microRNA miR-122 A cis-acting replication element in the sequence encoding the NS5B RNA-dependent RNA polymerase is required for hepatitis C virus RNA replication Crystal structure of the HCV IRES central domain reveals strategy for start-codon positioning Cis-acting RNA elements in human and animal plus-strand RNA viruses Characterizing the function and structural organization of the 5' tRNA-like motif within the hepatitis C virus quasispecies A hepatitis C virus (HCV) internal ribosome entry site (IRES) domain III-IV-targeted aptamer inhibits translation by binding to an apical loop of domain IIId The hepatitis C virus 3'-untranslated region or a poly(A) tract promote efficient translation subsequent to the initiation phase.A Tale of Two RNAs during Viral Infection: How Viruses Antagonize mRNAs and Small Non-Coding RNAs in The Host Cell Host-Targeting Agents to Prevent and Cure Hepatitis C Virus Infection The structures of nonprotein-coding RNAs that drive internal ribosome entry site function Complete translation of the hepatitis C virus genome in vitro: membranes play a critical role in the maturation of all virus proteins except for NS3.Hepatitis C virus internal ribosome entry site-dependent translation in Saccharomyces cerevisiae is independent of polypyrimidine tract-binding protein, poly(rC)-binding protein 2, and La protein Functional analyses of RNA structures shared between the internal ribosome entry sites of hepatitis C virus and the picornavirus porcine teschovirus 1 Talfan.Pestivirus internal ribosome entry site (IRES) structure and function: elements in the 5' untranslated region important for IRES function.The influence of downstream protein-coding sequence on internal ribosome entry on hepatitis C virus and other flavivirus RNAs Ribosomal proteins mediate the hepatitis C virus IRES-HeLa 40S interaction The influence of viral coding sequences on pestivirus IRES activity reveals further parallels with translation initiation in prokaryotes.Inhibition of the protein kinase PKR by the internal ribosome entry site of hepatitis C virus genomic RNA Antisense oligonucleotides targeted to the domain IIId of the hepatitis C virus IRES compete with 40S ribosomal subunit binding and prevent in vitro translation Proteins surrounding hairpin IIIe of the hepatitis C virus internal ribosome entry site on the human 40S ribosomal subunit Viral Internal Ribosome Entry Site Elements: Novel Ribosome-RNA Complexes and Roles in Viral Pathogenesis Searching for IRES Discovery of significant variants containing large deletions in the 5'UTR of human hepatitis C virus (HCV)Initiation of Protein Synthesis by Hepatitis C Virus Is Refractory to Reduced eIF2 {middle dot} GTP {middle dot} Met-tRNAiMet Ternary Complex Availability HCV and CSFV IRES domain II mediate eIF2 release during 80S ribosome assembly Small Interfering RNA Targeted to Hepatitis C Virus 5' Nontranslated Region Exerts Potent Antiviral Effect A Distinct Group of Hepacivirus/Pestivirus-Like Internal Ribosomal Entry Sites in Members of Diverse Picornavirus Genera: Evidence for Modular Exchange of Functional Noncoding RNA Elements by Recombination Studying Hepatitis C Virus: Making the Best of a Bad Virus Nuclear factors are involved in hepatitis C virus RNA replication Factor requirements for translation initiation on the Simian picornavirus internal ribosomal entry site The Picornavirus Avian Encephalomyelitis Virus Possesses a Hepatitis C Virus-Like Internal Ribosome Entry Site Element eIF2-dependent and eIF2-independent modes of initiation on the CSFV IRES: a common role of domain II Monocistronic mRNAs containing defective hepatitis C virus-like picornavirus internal ribosome entry site elements in their 5' untranslated regions are efficiently translated in cells by a cap-dependent mechanism High-Resolution Functional Profiling of Hepatitis C Virus Genome

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Mechanism of ribosome recruitment by hepatitis C IRES RNA

http://www.wikidata.org/entity/Q27472954

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2001 nî lūn-bûn

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2001 թուականի Փետրուարին հրատարակուած գիտական յօդուած

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2001 թվականի փետրվարին հրատարակված գիտական հոդված

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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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2001年学术文章

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2001年学术文章

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2001年學術文章

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name

Mechanism of ribosome recruitment by hepatitis C IRES RNA

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Mechanism of ribosome recruitment by hepatitis C IRES RNA

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Mechanism of ribosome recruitment by hepatitis C IRES RNA

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type

label

Mechanism of ribosome recruitment by hepatitis C IRES RNA

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Mechanism of ribosome recruitment by hepatitis C IRES RNA

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Mechanism of ribosome recruitment by hepatitis C IRES RNA

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prefLabel

Mechanism of ribosome recruitment by hepatitis C IRES RNA

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Mechanism of ribosome recruitment by hepatitis C IRES RNA

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Mechanism of ribosome recruitment by hepatitis C IRES RNA

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Mechanism of ribosome recruitment by hepatitis C IRES RNA

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J S Kieft

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K Zhou

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R Jubin

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P2860

Influence of correct secondary and tertiary RNA folding on the binding of cellular factors to the HCV IRES

A phylogenetically conserved stem-loop structure at the 5' border of the internal ribosome entry site of hepatitis C virus is required for cap-independent viral translation.

Alterations to both the primary and predicted secondary structure of stem-loop IIIc of the hepatitis C virus 1b 5' untranslated region (5'UTR) lead to mutants severely defective in translation which cannot be complemented in trans by the wild-type 5

Specific interaction of eukaryotic translation initiation factor 3 with the 5' nontranslated regions of hepatitis C virus and classical swine fever virus RNAs.

Heterogeneous nuclear ribonucleoprotein L interacts with the 3' border of the internal ribosomal entry site of hepatitis C virus

An enzymatic footprinting analysis of the interaction of 40S ribosomal subunits with the internal ribosomal entry site of hepatitis C virus

Internal initiation of translation of hepatitis C virus RNA: the ribosome entry site is at the authentic initiation codon.

Stability of a stem-loop involving the initiator AUG controls the efficiency of internal initiation of translation on hepatitis C virus RNA.

Functional analysis of the interaction between HCV 5'UTR and putative subunits of eukaryotic translation initiation factor eIF3

An RNA pseudoknot is an essential structural element of the internal ribosome entry site located within the hepatitis C virus 5' noncoding region

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Internal ribosome entry site

Hepatitis C virus

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