To Process or to Decay: A Mechanistic View of the Nuclear RNA Exosome.


Journal

Cold Spring Harbor symposia on quantitative biology
ISSN: 1943-4456
Titre abrégé: Cold Spring Harb Symp Quant Biol
Pays: United States
ID NLM: 1256107

Informations de publication

Date de publication:
2019
Historique:
pubmed: 5 6 2020
medline: 5 6 2020
entrez: 5 6 2020
Statut: ppublish

Résumé

The RNA exosome was originally discovered in yeast as an RNA-processing complex required for the maturation of 5.8S ribosomal RNA (rRNA), one of the constituents of the large ribosomal subunit. The exosome is now known in eukaryotes as the major 3'-5' RNA degradation machine involved in numerous processing, turnover, and surveillance pathways, both in the nucleus and the cytoplasm. Yet its role in maturing the 5.8S rRNA in the pre-60S ribosomal particle remains probably the most intricate and emblematic among its functions, as it involves all the RNA unwinding, degradation, and trimming activities embedded in this macromolecular complex. Here, we propose a comprehensive mechanistic model, based on current biochemical and structural data, explaining the dual functions of the nuclear exosome-the constructive versus the destructive mode.

Identifiants

pubmed: 32493762
pii: sqb.2019.84.040295
doi: 10.1101/sqb.2019.84.040295
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

155-163

Informations de copyright

© 2019 Lingaraju et al.; Published by Cold Spring Harbor Laboratory Press.

Auteurs

Mahesh Lingaraju (M)

Max-Planck-Institute of Biochemistry, Department of Structural Cell Biology, D-82152 Martinsried/Munich, Germany.

Jan M Schuller (JM)

Max-Planck-Institute of Biochemistry, Department of Structural Cell Biology, D-82152 Martinsried/Munich, Germany.

Sebastian Falk (S)

Max Perutz Labs, Department of Structural and Computational Biology, University of Vienna, 1030, Vienna, Austria.

Piotr Gerlach (P)

Max-Planck-Institute of Biochemistry, Department of Structural Cell Biology, D-82152 Martinsried/Munich, Germany.

Fabien Bonneau (F)

Max-Planck-Institute of Biochemistry, Department of Structural Cell Biology, D-82152 Martinsried/Munich, Germany.

Jérôme Basquin (J)

Max-Planck-Institute of Biochemistry, Department of Structural Cell Biology, D-82152 Martinsried/Munich, Germany.

Christian Benda (C)

Max-Planck-Institute of Biochemistry, Department of Structural Cell Biology, D-82152 Martinsried/Munich, Germany.

Elena Conti (E)

Max-Planck-Institute of Biochemistry, Department of Structural Cell Biology, D-82152 Martinsried/Munich, Germany.

Classifications MeSH