Genetic and genomic evolution of sexual reproduction: echoes from LECA to the fungal kingdom.


Journal

Current opinion in genetics & development
ISSN: 1879-0380
Titre abrégé: Curr Opin Genet Dev
Pays: England
ID NLM: 9111375

Informations de publication

Date de publication:
10 2019
Historique:
received: 01 05 2019
revised: 28 06 2019
accepted: 16 07 2019
pubmed: 2 9 2019
medline: 18 8 2020
entrez: 2 9 2019
Statut: ppublish

Résumé

Sexual reproduction is vastly diverse and yet highly conserved across the eukaryotic domain. This ubiquity suggests that the last eukaryotic common ancestor (LECA) was sexual. It is hypothesized that several critical processes in sexual reproduction, including cell fusion and meiosis, were acquired during the evolution from the first eukaryotic common ancestor (FECA) to the sexual LECA. However, it is challenging to delineate the exact origin and evolution of sexual reproduction given that both FECA and LECA are extinct. Studies of diverse eukaryotes have helped to shed light on this sexual evolutionary trajectory, revealing that a primordial sexual ploidy cycle likely involved endoreplication followed by concerted chromosome loss and that cell-cell fusion, meiosis, and sex determination later arose to shape modern sexual reproduction. Despite the general conservation of sexual reproduction processes throughout eukaryotes, modern sexual cycles are immensely diverse and complex. This diversity and complexity has become readily apparent in the fungal kingdom with the recent rapid expansion of whole-genome sequencing. This abundance of data, the variety of genetic tools available to manipulate and characterize fungi, and the thorough characterization of many fungal sexual cycles make the fungal kingdom an excellent forum, in which to study the conservation and diversification of sexual reproduction.

Identifiants

pubmed: 31473482
pii: S0959-437X(19)30035-8
doi: 10.1016/j.gde.2019.07.008
pmc: PMC6889014
mid: NIHMS1538616
pii:
doi:

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

70-75

Subventions

Organisme : NIAID NIH HHS
ID : F31 AI143136
Pays : United States
Organisme : NIAID NIH HHS
ID : R01 AI039115
Pays : United States
Organisme : NIAID NIH HHS
ID : R01 AI050113
Pays : United States
Organisme : NIAID NIH HHS
ID : R37 AI039115
Pays : United States

Informations de copyright

Copyright © 2019 Elsevier Ltd. All rights reserved.

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Auteurs

Ci Fu (C)

Department of Molecular Genetics and Microbiology, Duke University Medical Center, Durham, NC, 27710, USA.

Marco A Coelho (MA)

Department of Molecular Genetics and Microbiology, Duke University Medical Center, Durham, NC, 27710, USA.

Márcia David-Palma (M)

Department of Molecular Genetics and Microbiology, Duke University Medical Center, Durham, NC, 27710, USA.

Shelby J Priest (SJ)

Department of Molecular Genetics and Microbiology, Duke University Medical Center, Durham, NC, 27710, USA.

Joseph Heitman (J)

Department of Molecular Genetics and Microbiology, Duke University Medical Center, Durham, NC, 27710, USA. Electronic address: heitm001@duke.edu.

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Classifications MeSH