The Toxin-Antidote Model of Cytoplasmic Incompatibility: Genetics and Evolutionary Implications.

Animals Antidotes / chemistry Arthropods / genetics Bacterial Toxins / chemistry Culicidae / genetics Cytoplasm / genetics Drosophila / genetics Gene Transfer Techniques Symbiosis / genetics Vector Borne Diseases / genetics Wolbachia / genetics
Wolbachia cytoplasmic incompatibility deubiquitylase nuclease selfish genetic elements toxin–antidote systems

Journal

Trends in genetics : TIG
ISSN: 0168-9525
Titre abrégé: Trends Genet
Pays: England
ID NLM: 8507085

Informations de publication

Date de publication:
03 2019
Historique:
received: 27 10 2018
revised: 17 12 2018
accepted: 19 12 2018
pubmed: 28 1 2019
medline: 9 1 2020
entrez: 28 1 2019
Statut: ppublish

Résumé

Wolbachia bacteria inhabit the cells of about half of all arthropod species, an unparalleled success stemming in large part from selfish invasive strategies. Cytoplasmic incompatibility (CI), whereby the symbiont makes itself essential to embryo viability, is the most common of these and constitutes a promising weapon against vector-borne diseases. After decades of theoretical and experimental struggle, major recent advances have been made toward a molecular understanding of this phenomenon. As pieces of the puzzle come together, from yeast and Drosophila fly transgenesis to CI diversity patterns in natural mosquito populations, it becomes clearer than ever that the CI induction and rescue stem from a toxin-antidote (TA) system. Further, the tight association of the CI genes with prophages provides clues to the possible evolutionary origin of this phenomenon and the levels of selection at play.

Identifiants

DOI: 10.1016/j.tig.2018.12.004 PMID: 30685209 PMC: PMC6519454
pubmed: 30685209
pii: S0168-9525(18)30223-3
doi: 10.1016/j.tig.2018.12.004
pmc: PMC6519454
mid: NIHMS1023814
pii:
doi:

Substances chimiques

Antidotes 0
Bacterial Toxins 0

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

175-185

Subventions

Organisme : NIGMS NIH HHS
ID : R01 GM046904
Pays : United States
Organisme : NIGMS NIH HHS
ID : R01 GM053756
Pays : United States
Organisme : NIGMS NIH HHS
ID : R37 GM046904
Pays : United States

Informations de copyright

Copyright © 2018 Elsevier Ltd. All rights reserved.

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Auteurs

John F Beckmann (JF)

Auburn University, Department of Entomology and Plant Pathology, 301 Funchess Hall, Auburn, AL 36849, USA; Equal contribution.

Manon Bonneau (M)

Institut des Sciences de l'Evolution de Montpellier (ISEM), University of Montpellier, Centre National de la Recherche Scientifique (CNRS), Ecole Pratique des Hautes Etudes (EPHE), Institut de Recherche pour le Développement (IRD), Montpellier, France; Equal contribution.

Hongli Chen (H)

Yale University, Department of Molecular Biophysics and Biochemistry, 266 Whitney Avenue, New Haven, CT 06511, USA.

Mark Hochstrasser (M)

Yale University, Department of Molecular Biophysics and Biochemistry, 266 Whitney Avenue, New Haven, CT 06511, USA.

Denis Poinsot (D)

Université Rennes 1, Institut de Génétique, Environnement, et Protection des Plantes (IGEPP), Campus Beaulieu, 35042 Rennes, France.

Hervé Merçot (H)

Sorbonne Université, Université Pierre et Marie Curie (UPMC) Université Paris 06, CNRS, Institut de Biologie Paris Seine, Evolution Paris Seine (IBPS, EPS), 7-9 Quai St-Bernard, 75005 Paris, France.

Mylène Weill (M)

Institut des Sciences de l'Evolution de Montpellier (ISEM), University of Montpellier, Centre National de la Recherche Scientifique (CNRS), Ecole Pratique des Hautes Etudes (EPHE), Institut de Recherche pour le Développement (IRD), Montpellier, France.

Mathieu Sicard (M)

Institut des Sciences de l'Evolution de Montpellier (ISEM), University of Montpellier, Centre National de la Recherche Scientifique (CNRS), Ecole Pratique des Hautes Etudes (EPHE), Institut de Recherche pour le Développement (IRD), Montpellier, France. Electronic address: mathieu.sicard@umontpellier.fr.

Sylvain Charlat (S)

CNRS, University of Lyon, Laboratoire de Biométrie et Biologie Evolutive, 16 rue Raphael Dubois, 69622 Villeurbanne, France. Electronic address: sylvain.charlat@univ-lyon1.fr.

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Classifications MeSH

questionsmedicales.fr › Eucaryotes › Animaux › The Toxin-Antidote Model of Cytoplasmic...
questionsmedicales.fr › Actions chimiques et utilisations › Utilisations spécialisées de produits chimiques › Agents protecteurs › Antidotes › The Toxin-Antidote Model of Cytoplasmic...
questionsmedicales.fr › Eucaryotes › Animaux › Invertébrés › Arthropodes › The Toxin-Antidote Model of Cytoplasmic...
questionsmedicales.fr › Facteurs biologiques › Toxines biologiques › Toxines bactériennes › The Toxin-Antidote Model of Cytoplasmic...
questionsmedicales.fr › Eucaryotes › Animaux › Invertébrés › Arthropodes › Insectes › Pterygota › Neoptera › Holometabola › Diptera › Nematocera › Culicomorpha › Culicidae › The Toxin-Antidote Model of Cytoplasmic...
questionsmedicales.fr › Cellules › Structures cellulaires › Espace intracellulaire › Cytoplasme › The Toxin-Antidote Model of Cytoplasmic...
questionsmedicales.fr › Eucaryotes › Animaux › Invertébrés › Arthropodes › Insectes › Pterygota › Neoptera › Holometabola › Diptera › Drosophilidae › Drosophila › The Toxin-Antidote Model of Cytoplasmic...
questionsmedicales.fr › Techniques d'investigation › Techniques génétiques › Techniques de transfert de gènes › The Toxin-Antidote Model of Cytoplasmic...
questionsmedicales.fr › Phénomènes biologiques › Symbiose › The Toxin-Antidote Model of Cytoplasmic...
questionsmedicales.fr › Infection › Maladies vectorielles › The Toxin-Antidote Model of Cytoplasmic...
questionsmedicales.fr › Bactéries › Proteobacteria › Alphaproteobacteria › Rickettsiales › Anaplasmataceae › Wolbachia › The Toxin-Antidote Model of Cytoplasmic...