Structures and functions of short argonautes.


Journal

RNA biology
ISSN: 1555-8584
Titre abrégé: RNA Biol
Pays: United States
ID NLM: 101235328

Informations de publication

Date de publication:
Jan 2024
Historique:
medline: 2 9 2024
pubmed: 2 9 2024
entrez: 2 9 2024
Statut: ppublish

Résumé

Argonaute proteins (Agos) represent a highly conserved family of proteins prevalent in all domains of life and have been implicated in various biological processes. Based on the domain architecture, Agos can be divided into long Agos and short Agos. While long Agos have been extensively studied over the past two decades, short Agos, found exclusively in prokaryotes, have recently gained attention for their roles in prokaryotic immune defence against mobile genetic elements, such as plasmids and phages. Notable functional and structural studies provide invaluable insights into the underlying molecular mechanisms of representative short Ago systems. Despite the diverse domain arrangements, short Agos generally form heterodimeric complexes with their associated effector proteins, activating the effector's enzymatic activities upon target detection. The activation of effector proteins in the short Ago systems leads to bacterial cell death, a mechanism of sacrificing individuals to protect the community.

Identifiants

pubmed: 39219231
doi: 10.1080/15476286.2024.2380948
doi:

Substances chimiques

Argonaute Proteins 0
Bacterial Proteins 0

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

1-7

Auteurs

Chen Wang (C)

Department of Biological Chemistry and Pharmacology, Center for RNA Biology, The Ohio State University, Columbus, OH, USA.
The Ohio State University Comprehensive Cancer Center, Columbus, OH, USA.

Zhangfei Shen (Z)

Department of Biological Chemistry and Pharmacology, Center for RNA Biology, The Ohio State University, Columbus, OH, USA.
The Ohio State University Comprehensive Cancer Center, Columbus, OH, USA.

Xiao-Yuan Yang (XY)

Department of Biological Chemistry and Pharmacology, Center for RNA Biology, The Ohio State University, Columbus, OH, USA.
The Ohio State University Comprehensive Cancer Center, Columbus, OH, USA.
Program of OSBP, The Ohio State University, Columbus, OH, USA.

Tian-Min Fu (TM)

Department of Biological Chemistry and Pharmacology, Center for RNA Biology, The Ohio State University, Columbus, OH, USA.
The Ohio State University Comprehensive Cancer Center, Columbus, OH, USA.
Program of OSBP, The Ohio State University, Columbus, OH, USA.

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Classifications MeSH