In vivo targeting of the yeast Pop2 deadenylase subunit to reporter transcripts induces their rapid degradation and generates new decay intermediates

Journal of Biological Chemistry

Volumn 281, Issue 36, 2006, Pages 25940-25947

  Finoux, Anne Laure ^a   Séraphin, Bertrand ^a  

^a CENTRE DE GÉNÉTIQUE MOLÉCULAIRE   (France)

Author keywords

[No Author keywords available]

Indexed keywords

BINDING SITES; EXOSOME; POP2 DEADENYLASE;

BIOCHEMISTRY; BIODEGRADATION; ENZYMES; GROWTH KINETICS; RNA;

YEAST;

DEADENYLASE; FUNGAL ENZYME; MESSENGER RNA; UNCLASSIFIED DRUG;

3' UNTRANSLATED REGION; ARTICLE; BINDING SITE; CHEMICAL MODIFICATION; CONTROLLED STUDY; DEADENYLATION; ENZYME ACTIVATION; ENZYME ACTIVITY; ENZYME REGULATION; ENZYME SUBUNIT; GENE CONSTRUCT; GENE EXPRESSION REGULATION; GENE TARGETING; GENETIC TRANSCRIPTION; IN VIVO STUDY; NONHUMAN; PRIORITY JOURNAL; PROTEIN DOMAIN; PROTEIN TARGETING; RNA BINDING; RNA DEGRADATION;

ANIMALS; BASE SEQUENCE; FUNGAL PROTEINS; GENES, REPORTER; HUMANS; MOLECULAR SEQUENCE DATA; NUCLEIC ACID CONFORMATION; PROTEIN SUBUNITS; RECOMBINANT FUSION PROTEINS; RIBONUCLEASES; RIBONUCLEOPROTEIN, U1 SMALL NUCLEAR; RNA, MESSENGER; RNA-BINDING PROTEINS; SACCHAROMYCES CEREVISIAE PROTEINS;

EID: 33748746509     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.M600132200     Document Type: Article

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