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Interaction of nucleolin with an evolutionarily conserved pre-ribosomal RNA sequence is required for the assembly of the primary processing complex.
Ginisty, H; Serin, G; Ghisolfi-Nieto, L; Roger, B; Libante, V; Amalric, F; Bouvet, P.
Affiliation
  • Ginisty H; Laboratoire de Pharmacologie et de Biologie Structurale, CNRS UMR 5089, 205 route de Narbonne, 31077 Toulouse Cedex, France.
J Biol Chem ; 275(25): 18845-50, 2000 Jun 23.
Article in En | MEDLINE | ID: mdl-10858445
ABSTRACT
The first processing event of the precursor ribosomal RNA (pre-rRNA) takes place within the 5' external transcribed spacer. This primary processing requires conserved cis-acting RNA sequence downstream from the cleavage site and several nucleic acids (small nucleolar RNAs) and proteins trans-acting factors including nucleolin, a major nucleolar protein. The specific interaction of nucleolin with the pre-rRNA is required for processing in vitro. Xenopus laevis and hamster nucleolin interact with the same pre-rRNA site and stimulate the processing activity of a mouse cell extract. A highly conserved 11-nucleotide sequence located 5-6 nucleotides after the processing site is required for the interaction of nucleolin and processing. In vitro selection experiments with nucleolin have identified an RNA sequence that contains the UCGA motif present in the 11-nucleotide conserved sequence. The interaction of nucleolin with pre-rRNA is required for the formation of an active processing complex. Our findings demonstrate that nucleolin is a key factor for the assembly and maturation of pre-ribosomal ribonucleoparticles.
Subject(s)
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Collection: 01-internacional Database: MEDLINE Main subject: Phosphoproteins / RNA, Ribosomal / RNA-Binding Proteins Type of study: Prognostic_studies Limits: Animals Language: En Journal: J Biol Chem Year: 2000 Document type: Article Affiliation country: France
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Collection: 01-internacional Database: MEDLINE Main subject: Phosphoproteins / RNA, Ribosomal / RNA-Binding Proteins Type of study: Prognostic_studies Limits: Animals Language: En Journal: J Biol Chem Year: 2000 Document type: Article Affiliation country: France
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