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Structural basis of human U5 snRNP late biogenesis and recycling.
Riabov Bassat, Daria; Visanpattanasin, Supapat; Vorländer, Matthias K; Fin, Laura; Phillips, Alexander W; Plaschka, Clemens.
Afiliación
  • Riabov Bassat D; Research Institute of Molecular Pathology, Vienna BioCenter, Vienna, Austria.
  • Visanpattanasin S; Research Institute of Molecular Pathology, Vienna BioCenter, Vienna, Austria.
  • Vorländer MK; Research Institute of Molecular Pathology, Vienna BioCenter, Vienna, Austria.
  • Fin L; Research Institute of Molecular Pathology, Vienna BioCenter, Vienna, Austria.
  • Phillips AW; Research Institute of Molecular Pathology, Vienna BioCenter, Vienna, Austria.
  • Plaschka C; Vienna BioCenter PhD Program, Doctoral School of the University of Vienna and Medical University of Vienna, Vienna, Austria.
Nat Struct Mol Biol ; 31(5): 747-751, 2024 May.
Article en En | MEDLINE | ID: mdl-38467876
ABSTRACT
Pre-mRNA splicing by the spliceosome requires the biogenesis and recycling of its small nuclear ribonucleoprotein (snRNP) complexes, which are consumed in each round of splicing. The human U5 snRNP is the ~1 MDa 'heart' of the spliceosome and is recycled through an unknown mechanism involving major architectural rearrangements and the dedicated chaperones CD2BP2 and TSSC4. Late steps in U5 snRNP biogenesis similarly involve these chaperones. Here we report cryo-electron microscopy structures of four human U5 snRNP-CD2BP2-TSSC4 complexes, revealing how a series of molecular events primes the U5 snRNP to generate the ~2 MDa U4/U6.U5 tri-snRNP, the largest building block of the spliceosome.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Modelos Moleculares / Empalmosomas / Ribonucleoproteína Nuclear Pequeña U5 / Microscopía por Crioelectrón Límite: Humans Idioma: En Revista: Nat Struct Mol Biol Asunto de la revista: BIOLOGIA MOLECULAR Año: 2024 Tipo del documento: Article País de afiliación: Austria

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Modelos Moleculares / Empalmosomas / Ribonucleoproteína Nuclear Pequeña U5 / Microscopía por Crioelectrón Límite: Humans Idioma: En Revista: Nat Struct Mol Biol Asunto de la revista: BIOLOGIA MOLECULAR Año: 2024 Tipo del documento: Article País de afiliación: Austria