Cargando…

Multiple Molecular Mechanisms Cause Reproductive Isolation between Three Yeast Species

Nuclear-mitochondrial conflict (cytonuclear incompatibility) is a specific form of Dobzhansky-Muller incompatibility previously shown to cause reproductive isolation in two yeast species. Here, we identified two new incompatible genes, MRS1 and AIM22, through a systematic study of F2 hybrid sterilit...

Descripción completa

Detalles Bibliográficos
Autores principales: Chou, Jui-Yu, Hung, Yin-Shan, Lin, Kuan-Huei, Lee, Hsin-Yi, Leu, Jun-Yi
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2907292/
https://www.ncbi.nlm.nih.gov/pubmed/20652018
http://dx.doi.org/10.1371/journal.pbio.1000432
_version_ 1782184091360165888
author Chou, Jui-Yu
Hung, Yin-Shan
Lin, Kuan-Huei
Lee, Hsin-Yi
Leu, Jun-Yi
author_facet Chou, Jui-Yu
Hung, Yin-Shan
Lin, Kuan-Huei
Lee, Hsin-Yi
Leu, Jun-Yi
author_sort Chou, Jui-Yu
collection PubMed
description Nuclear-mitochondrial conflict (cytonuclear incompatibility) is a specific form of Dobzhansky-Muller incompatibility previously shown to cause reproductive isolation in two yeast species. Here, we identified two new incompatible genes, MRS1 and AIM22, through a systematic study of F2 hybrid sterility caused by cytonuclear incompatibility in three closely related Saccharomyces species (S. cerevisiae, S. paradoxus, and S. bayanus). Mrs1 is a nuclear gene product required for splicing specific introns in the mitochondrial COX1, and Aim22 is a ligase encoded in the nucleus that is required for mitochondrial protein lipoylation. By comparing different species, our result suggests that the functional changes in MRS1 are a result of coevolution with changes in the COX1 introns. Further molecular analyses demonstrate that three nonsynonymous mutations are responsible for the functional differences of Mrs1 between these species. Functional complementation assays to determine when these incompatible genes altered their functions show a strong correlation between the sequence-based phylogeny and the evolution of cytonuclear incompatibility. Our results suggest that nuclear-mitochondrial incompatibility may represent a general mechanism of reproductive isolation during yeast evolution.
format Text
id pubmed-2907292
institution National Center for Biotechnology Information
language English
publishDate 2010
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-29072922010-07-22 Multiple Molecular Mechanisms Cause Reproductive Isolation between Three Yeast Species Chou, Jui-Yu Hung, Yin-Shan Lin, Kuan-Huei Lee, Hsin-Yi Leu, Jun-Yi PLoS Biol Research Article Nuclear-mitochondrial conflict (cytonuclear incompatibility) is a specific form of Dobzhansky-Muller incompatibility previously shown to cause reproductive isolation in two yeast species. Here, we identified two new incompatible genes, MRS1 and AIM22, through a systematic study of F2 hybrid sterility caused by cytonuclear incompatibility in three closely related Saccharomyces species (S. cerevisiae, S. paradoxus, and S. bayanus). Mrs1 is a nuclear gene product required for splicing specific introns in the mitochondrial COX1, and Aim22 is a ligase encoded in the nucleus that is required for mitochondrial protein lipoylation. By comparing different species, our result suggests that the functional changes in MRS1 are a result of coevolution with changes in the COX1 introns. Further molecular analyses demonstrate that three nonsynonymous mutations are responsible for the functional differences of Mrs1 between these species. Functional complementation assays to determine when these incompatible genes altered their functions show a strong correlation between the sequence-based phylogeny and the evolution of cytonuclear incompatibility. Our results suggest that nuclear-mitochondrial incompatibility may represent a general mechanism of reproductive isolation during yeast evolution. Public Library of Science 2010-07-20 /pmc/articles/PMC2907292/ /pubmed/20652018 http://dx.doi.org/10.1371/journal.pbio.1000432 Text en Chou et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Chou, Jui-Yu
Hung, Yin-Shan
Lin, Kuan-Huei
Lee, Hsin-Yi
Leu, Jun-Yi
Multiple Molecular Mechanisms Cause Reproductive Isolation between Three Yeast Species
title Multiple Molecular Mechanisms Cause Reproductive Isolation between Three Yeast Species
title_full Multiple Molecular Mechanisms Cause Reproductive Isolation between Three Yeast Species
title_fullStr Multiple Molecular Mechanisms Cause Reproductive Isolation between Three Yeast Species
title_full_unstemmed Multiple Molecular Mechanisms Cause Reproductive Isolation between Three Yeast Species
title_short Multiple Molecular Mechanisms Cause Reproductive Isolation between Three Yeast Species
title_sort multiple molecular mechanisms cause reproductive isolation between three yeast species
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2907292/
https://www.ncbi.nlm.nih.gov/pubmed/20652018
http://dx.doi.org/10.1371/journal.pbio.1000432
work_keys_str_mv AT choujuiyu multiplemolecularmechanismscausereproductiveisolationbetweenthreeyeastspecies
AT hungyinshan multiplemolecularmechanismscausereproductiveisolationbetweenthreeyeastspecies
AT linkuanhuei multiplemolecularmechanismscausereproductiveisolationbetweenthreeyeastspecies
AT leehsinyi multiplemolecularmechanismscausereproductiveisolationbetweenthreeyeastspecies
AT leujunyi multiplemolecularmechanismscausereproductiveisolationbetweenthreeyeastspecies