ADP-ribosylation systems in bacteria and viruses.

ADP-ribosyl hydrolase ADP-ribosyl transferase ADP-ribosylation Macrodomain PARP, PARG Toxin-antitoxin system

Journal

Computational and structural biotechnology journal
ISSN: 2001-0370
Titre abrégé: Comput Struct Biotechnol J
Pays: Netherlands
ID NLM: 101585369

Informations de publication

Date de publication:
2021
Historique:
received: 01 02 2021
revised: 07 04 2021
accepted: 07 04 2021
entrez: 24 5 2021
pubmed: 25 5 2021
medline: 25 5 2021
Statut: epublish

Résumé

ADP-ribosylation is an ancient posttranslational modification present in all kingdoms of life. The system likely originated in bacteria where it functions in inter- and intra-species conflict, stress response and pathogenicity. It was repeatedly adopted via lateral transfer by eukaryotes, including humans, where it has a pivotal role in epigenetics, DNA-damage repair, apoptosis, and other crucial pathways including the immune response to pathogenic bacteria and viruses. In other words, the same ammunition used by pathogens is adapted by eukaryotes to fight back. While we know quite a lot about the eukaryotic system, expanding rather patchy knowledge on bacterial and viral ADP-ribosylation would give us not only a better understanding of the system as a whole but a fighting advantage in this constant arms race. By writing this review we hope to put into focus the available information and give a perspective on how this system works and can be exploited in the search for therapeutic targets in the future. The relevance of the subject is especially highlighted by the current situation of being amid the world pandemic caused by a virus harbouring and dependent on a representative of such a system.

Identifiants

pubmed: 34025930
doi: 10.1016/j.csbj.2021.04.023
pii: S2001-0370(21)00135-5
pmc: PMC8120803
doi:

Types de publication

Journal Article Review

Langues

eng

Pagination

2366-2383

Informations de copyright

© 2021 The Author(s).

Déclaration de conflit d'intérêts

The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

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Auteurs

Petra Mikolčević (P)

Division of Molecular Biology, Ruđer Bošković Institute, Zagreb, Croatia.

Andrea Hloušek-Kasun (A)

Division of Molecular Biology, Ruđer Bošković Institute, Zagreb, Croatia.

Ivan Ahel (I)

Sir William Dunn School of Pathology, University of Oxford, UK.

Andreja Mikoč (A)

Division of Molecular Biology, Ruđer Bošković Institute, Zagreb, Croatia.

Classifications MeSH