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Intron lariat spliceosomes convert lariats to true circles: implications for intron transposition.
Ares, Manuel; Igel, Haller; Katzman, Sol; Donohue, John P.
Afiliação
  • Ares M; Center for Molecular Biology of RNA, University of California, Santa Cruz, Santa Cruz, California 95064, USA; ares@ucsc.edu.
  • Igel H; Genomics Institute, University of California, Santa Cruz, Santa Cruz, California 95064, USA.
  • Katzman S; Center for Molecular Biology of RNA, University of California, Santa Cruz, Santa Cruz, California 95064, USA.
  • Donohue JP; Center for Molecular Biology of RNA, University of California, Santa Cruz, Santa Cruz, California 95064, USA.
Genes Dev ; 38(7-8): 322-335, 2024 05 21.
Article em En | MEDLINE | ID: mdl-38724209
ABSTRACT
Rare, full-length circular intron RNAs distinct from lariats have been reported in several species, but their biogenesis is not understood. We envisioned and tested a hypothesis for their formation using Saccharomyces cerevisiae, documenting full-length and novel processed circular RNAs from multiple introns. Evidence implicates a previously undescribed catalytic activity of the intron lariat spliceosome (ILS) in which the 3'-OH of the lariat tail (with optional trimming and adenylation by the nuclear 3' processing machinery) attacks the branch, joining the intron 3' end to the 5' splice site in a 3'-5' linked circle. Human U2 and U12 spliceosomes produce analogous full-length and processed circles. Postsplicing catalytic activity of the spliceosome may promote intron transposition during eukaryotic genome evolution.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Saccharomyces cerevisiae / Íntrons / Splicing de RNA / Spliceossomos Limite: Humans Idioma: En Revista: Genes Dev Assunto da revista: BIOLOGIA MOLECULAR Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Saccharomyces cerevisiae / Íntrons / Splicing de RNA / Spliceossomos Limite: Humans Idioma: En Revista: Genes Dev Assunto da revista: BIOLOGIA MOLECULAR Ano de publicação: 2024 Tipo de documento: Article
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