P-body components are required for Ty1 retrotransposition during assembly of retrotransposition-competent virus-like particles. - Wikidata - wikimedia - TriplyDB

P-body components are required for Ty1 retrotransposition during assembly of retrotransposition-competent virus-like particles.

P-body components are required for Ty1 retrotransposition during assembly of retrotransposition-competent virus-like particles.

http://www.wikidata.org/entity/Q33558809

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Characterization of LINE-1 ribonucleoprotein particles The DEAD-box RNA helicase DDX6 is required for efficient encapsidation of a retroviral genome HIV-1 replication and APOBEC3 antiviral activity are not regulated by P bodies Determinants of Genomic RNA Encapsidation in the Saccharomyces cerevisiae Long Terminal Repeat Retrotransposons Ty1 and Ty3 Restricting retrotransposons: a review Nuclear trafficking of retroviral RNAs and Gag proteins during late steps of replication Preferential retrotransposition in aging yeast mother cells is correlated with increased genome instability.XRN1 Is a Species-Specific Virus Restriction Factor in Yeasts Co-translational localization of an LTR-retrotransposon RNA to the endoplasmic reticulum nucleates virus-like particle assembly sites Mapping the LINE1 ORF1 protein interactome reveals associated inhibitors of human retrotransposition Poliovirus-mediated disruption of cytoplasmic processing bodies Perturbation of the P-body component Mov10 inhibits HIV-1 infectivity.5' to 3' mRNA decay factors colocalize with Ty1 gag and human APOBEC3G and promote Ty1 retrotransposition.Non-long terminal repeat (non-LTR) retrotransposons: mechanisms, recent developments, and unanswered questions.Dynamic profiling of mRNA turnover reveals gene-specific and system-wide regulation of mRNA decay.HIV-1 Gag co-opts a cellular complex containing DDX6, a helicase that facilitates capsid assembly Role of the DHH1 gene in the regulation of monocarboxylic acids transporters expression in Saccharomyces cerevisiae.MOV10 RNA helicase is a potent inhibitor of retrotransposition in cells.HIV-2 genomic RNA accumulates in stress granules in the absence of active translation.Function of a retrotransposon nucleocapsid protein BARE retrotransposons are translated and replicated via distinct RNA pools.T-body formation precedes virus-like particle maturation in S. cerevisiae The Ty1 LTR-retrotransposon of budding yeast, Saccharomyces cerevisiae A trans-dominant form of Gag restricts Ty1 retrotransposition and mediates copy number control.A role for the budding yeast separase, Esp1, in Ty1 element retrotransposition.Retrotransposition is associated with genome instability during chronological aging.Ty3 Retrotransposon Hijacks Mating Yeast RNA Processing Bodies to Infect New Genomes.The Ty1 Retrotransposon Restriction Factor p22 Targets Gag.Tye7 regulates yeast Ty1 retrotransposon sense and antisense transcription in response to adenylic nucleotides stress.Proteomic Analysis of Dhh1 Complexes Reveals a Role for Hsp40 Chaperone Ydj1 in Yeast P-Body Assembly.Ribosomal protein and biogenesis factors affect multiple steps during movement of the Saccharomyces cerevisiae Ty1 retrotransposon.Ty1 gag enhances the stability and nuclear export of Ty1 mRNA.Sequence requirements for localization and packaging of Ty3 retroelement RNA.A self-encoded capsid derivative restricts Ty1 retrotransposition in Saccharomyces What might retrotransposons teach us about aging?A murine retrovirus co-Opts YB-1, a translational regulator and stress granule-associated protein, to facilitate virus assembly.The histone methyltransferases Set5 and Set1 have overlapping functions in gene silencing and telomere maintenance.P bodies inhibit retrotransposition of endogenous intracisternal a particles.Manipulation of cellular processing bodies and their constituents by viruses.Paralog-Specific Functions of RPL7A and RPL7B Mediated by Ribosomal Protein or snoRNA Dosage in Saccharomyces cerevisiae

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P2860

P-body components are required for Ty1 retrotransposition during assembly of retrotransposition-competent virus-like particles.

http://www.wikidata.org/entity/Q33558809

description

2009 nî lūn-bûn

@nan

2009 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած

@hyw

2009 թվականի նոյեմբերին հրատարակված գիտական հոդված

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2009年の論文

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2009年学术文章

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2009年学术文章

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2009年学术文章

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2009年学术文章

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2009年学术文章

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2009年學術文章

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name

P-body components are required ...... ompetent virus-like particles.

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P-body components are required ...... ompetent virus-like particles.

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P-body components are required ...... ompetent virus-like particles.

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type

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P-body components are required ...... ompetent virus-like particles.

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P-body components are required ...... ompetent virus-like particles.

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P-body components are required ...... ompetent virus-like particles.

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prefLabel

P-body components are required ...... ompetent virus-like particles.

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P-body components are required ...... ompetent virus-like particles.

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P-body components are required ...... ompetent virus-like particles.

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Molecular and Cellular Biology

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P-body components are required ...... ompetent virus-like particles.

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P2093

David J Garfinkel

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

Katherine M Nyswaner

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Kunio Nagashima

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

Mary Ann Checkley

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

Stephen J Lockett

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

P2860

Functional profiling of the Saccharomyces cerevisiae genome

Additional modules for versatile and economical PCR-based gene deletion and modification in Saccharomyces cerevisiae

Mating type switching in yeast controlled by asymmetric localization of ASH1 mRNA.

Decapping and decay of messenger RNA occur in cytoplasmic processing bodies

Multiple regulators of Ty1 transposition in Saccharomyces cerevisiae have conserved roles in genome maintenance.

Posttranslational regulation of Ty1 retrotransposition by mitogen-activated protein kinase Fus3

New heterologous modules for classical or PCR-based gene disruptions in Saccharomyces cerevisiae

Designer deletion strains derived from Saccharomyces cerevisiae S288C: a useful set of strains and plasmids for PCR-mediated gene disruption and other applications

Movement of eukaryotic mRNAs between polysomes and cytoplasmic processing bodies

P bodies and the control of mRNA translation and degradation

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382-398

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scholarly article

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10.1128/MCB.00251-09

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2

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30

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2009-11-09T00:00:00Z

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19901074

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2798465

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