Cargando…

A Case of Gene Fragmentation in Plant Mitochondria Fixed by the Selection of a Compensatory Restorer of Fertility-Like PPR Gene

The high mutational load of mitochondrial genomes combined with their uniparental inheritance and high polyploidy favors the maintenance of deleterious mutations within populations. How cells compose and adapt to the accumulation of disadvantageous mitochondrial alleles remains unclear. Most harmful...

Descripción completa

Detalles Bibliográficos
Autores principales: Nguyen, Tan-Trung, Planchard, Noelya, Dahan, Jennifer, Arnal, Nadège, Balzergue, Sandrine, Benamar, Abdelilah, Bertin, Pierre, Brunaud, Véronique, Dargel-Graffin, Céline, Macherel, David, Martin-Magniette, Marie-Laure, Quadrado, Martine, Namy, Olivier, Mireau, Hakim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8321540/
https://www.ncbi.nlm.nih.gov/pubmed/33878189
http://dx.doi.org/10.1093/molbev/msab115
_version_ 1783730874447036416
author Nguyen, Tan-Trung
Planchard, Noelya
Dahan, Jennifer
Arnal, Nadège
Balzergue, Sandrine
Benamar, Abdelilah
Bertin, Pierre
Brunaud, Véronique
Dargel-Graffin, Céline
Macherel, David
Martin-Magniette, Marie-Laure
Quadrado, Martine
Namy, Olivier
Mireau, Hakim
author_facet Nguyen, Tan-Trung
Planchard, Noelya
Dahan, Jennifer
Arnal, Nadège
Balzergue, Sandrine
Benamar, Abdelilah
Bertin, Pierre
Brunaud, Véronique
Dargel-Graffin, Céline
Macherel, David
Martin-Magniette, Marie-Laure
Quadrado, Martine
Namy, Olivier
Mireau, Hakim
author_sort Nguyen, Tan-Trung
collection PubMed
description The high mutational load of mitochondrial genomes combined with their uniparental inheritance and high polyploidy favors the maintenance of deleterious mutations within populations. How cells compose and adapt to the accumulation of disadvantageous mitochondrial alleles remains unclear. Most harmful changes are likely corrected by purifying selection, however, the intimate collaboration between mitochondria- and nuclear-encoded gene products offers theoretical potential for compensatory adaptive changes. In plants, cytoplasmic male sterilities are known examples of nucleo-mitochondrial coadaptation situations in which nuclear-encoded restorer of fertility (Rf) genes evolve to counteract the effect of mitochondria-encoded cytoplasmic male sterility (CMS) genes and restore fertility. Most cloned Rfs belong to a small monophyletic group, comprising 26 pentatricopeptide repeat genes in Arabidopsis, called Rf-like (RFL). In this analysis, we explored the functional diversity of RFL genes in Arabidopsis and found that the RFL8 gene is not related to CMS suppression but essential for plant embryo development. In vitro-rescued rfl8 plantlets are deficient in the production of the mitochondrial heme–lyase complex. A complete ensemble of molecular and genetic analyses allowed us to demonstrate that the RFL8 gene has been selected to permit the translation of the mitochondrial ccmF(N2) gene encoding a heme–lyase complex subunit which derives from the split of the ccmF(N) gene, specifically in Brassicaceae plants. This study represents thus a clear case of nuclear compensation to a lineage-specific mitochondrial genomic rearrangement in plants and demonstrates that RFL genes can be selected in response to other mitochondrial deviancies than CMS suppression.
format Online
Article
Text
id pubmed-8321540
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-83215402021-07-30 A Case of Gene Fragmentation in Plant Mitochondria Fixed by the Selection of a Compensatory Restorer of Fertility-Like PPR Gene Nguyen, Tan-Trung Planchard, Noelya Dahan, Jennifer Arnal, Nadège Balzergue, Sandrine Benamar, Abdelilah Bertin, Pierre Brunaud, Véronique Dargel-Graffin, Céline Macherel, David Martin-Magniette, Marie-Laure Quadrado, Martine Namy, Olivier Mireau, Hakim Mol Biol Evol Discoveries The high mutational load of mitochondrial genomes combined with their uniparental inheritance and high polyploidy favors the maintenance of deleterious mutations within populations. How cells compose and adapt to the accumulation of disadvantageous mitochondrial alleles remains unclear. Most harmful changes are likely corrected by purifying selection, however, the intimate collaboration between mitochondria- and nuclear-encoded gene products offers theoretical potential for compensatory adaptive changes. In plants, cytoplasmic male sterilities are known examples of nucleo-mitochondrial coadaptation situations in which nuclear-encoded restorer of fertility (Rf) genes evolve to counteract the effect of mitochondria-encoded cytoplasmic male sterility (CMS) genes and restore fertility. Most cloned Rfs belong to a small monophyletic group, comprising 26 pentatricopeptide repeat genes in Arabidopsis, called Rf-like (RFL). In this analysis, we explored the functional diversity of RFL genes in Arabidopsis and found that the RFL8 gene is not related to CMS suppression but essential for plant embryo development. In vitro-rescued rfl8 plantlets are deficient in the production of the mitochondrial heme–lyase complex. A complete ensemble of molecular and genetic analyses allowed us to demonstrate that the RFL8 gene has been selected to permit the translation of the mitochondrial ccmF(N2) gene encoding a heme–lyase complex subunit which derives from the split of the ccmF(N) gene, specifically in Brassicaceae plants. This study represents thus a clear case of nuclear compensation to a lineage-specific mitochondrial genomic rearrangement in plants and demonstrates that RFL genes can be selected in response to other mitochondrial deviancies than CMS suppression. Oxford University Press 2021-04-20 /pmc/articles/PMC8321540/ /pubmed/33878189 http://dx.doi.org/10.1093/molbev/msab115 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Discoveries
Nguyen, Tan-Trung
Planchard, Noelya
Dahan, Jennifer
Arnal, Nadège
Balzergue, Sandrine
Benamar, Abdelilah
Bertin, Pierre
Brunaud, Véronique
Dargel-Graffin, Céline
Macherel, David
Martin-Magniette, Marie-Laure
Quadrado, Martine
Namy, Olivier
Mireau, Hakim
A Case of Gene Fragmentation in Plant Mitochondria Fixed by the Selection of a Compensatory Restorer of Fertility-Like PPR Gene
title A Case of Gene Fragmentation in Plant Mitochondria Fixed by the Selection of a Compensatory Restorer of Fertility-Like PPR Gene
title_full A Case of Gene Fragmentation in Plant Mitochondria Fixed by the Selection of a Compensatory Restorer of Fertility-Like PPR Gene
title_fullStr A Case of Gene Fragmentation in Plant Mitochondria Fixed by the Selection of a Compensatory Restorer of Fertility-Like PPR Gene
title_full_unstemmed A Case of Gene Fragmentation in Plant Mitochondria Fixed by the Selection of a Compensatory Restorer of Fertility-Like PPR Gene
title_short A Case of Gene Fragmentation in Plant Mitochondria Fixed by the Selection of a Compensatory Restorer of Fertility-Like PPR Gene
title_sort case of gene fragmentation in plant mitochondria fixed by the selection of a compensatory restorer of fertility-like ppr gene
topic Discoveries
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8321540/
https://www.ncbi.nlm.nih.gov/pubmed/33878189
http://dx.doi.org/10.1093/molbev/msab115
work_keys_str_mv AT nguyentantrung acaseofgenefragmentationinplantmitochondriafixedbytheselectionofacompensatoryrestoreroffertilitylikepprgene
AT planchardnoelya acaseofgenefragmentationinplantmitochondriafixedbytheselectionofacompensatoryrestoreroffertilitylikepprgene
AT dahanjennifer acaseofgenefragmentationinplantmitochondriafixedbytheselectionofacompensatoryrestoreroffertilitylikepprgene
AT arnalnadege acaseofgenefragmentationinplantmitochondriafixedbytheselectionofacompensatoryrestoreroffertilitylikepprgene
AT balzerguesandrine acaseofgenefragmentationinplantmitochondriafixedbytheselectionofacompensatoryrestoreroffertilitylikepprgene
AT benamarabdelilah acaseofgenefragmentationinplantmitochondriafixedbytheselectionofacompensatoryrestoreroffertilitylikepprgene
AT bertinpierre acaseofgenefragmentationinplantmitochondriafixedbytheselectionofacompensatoryrestoreroffertilitylikepprgene
AT brunaudveronique acaseofgenefragmentationinplantmitochondriafixedbytheselectionofacompensatoryrestoreroffertilitylikepprgene
AT dargelgraffinceline acaseofgenefragmentationinplantmitochondriafixedbytheselectionofacompensatoryrestoreroffertilitylikepprgene
AT machereldavid acaseofgenefragmentationinplantmitochondriafixedbytheselectionofacompensatoryrestoreroffertilitylikepprgene
AT martinmagniettemarielaure acaseofgenefragmentationinplantmitochondriafixedbytheselectionofacompensatoryrestoreroffertilitylikepprgene
AT quadradomartine acaseofgenefragmentationinplantmitochondriafixedbytheselectionofacompensatoryrestoreroffertilitylikepprgene
AT namyolivier acaseofgenefragmentationinplantmitochondriafixedbytheselectionofacompensatoryrestoreroffertilitylikepprgene
AT mireauhakim acaseofgenefragmentationinplantmitochondriafixedbytheselectionofacompensatoryrestoreroffertilitylikepprgene
AT nguyentantrung caseofgenefragmentationinplantmitochondriafixedbytheselectionofacompensatoryrestoreroffertilitylikepprgene
AT planchardnoelya caseofgenefragmentationinplantmitochondriafixedbytheselectionofacompensatoryrestoreroffertilitylikepprgene
AT dahanjennifer caseofgenefragmentationinplantmitochondriafixedbytheselectionofacompensatoryrestoreroffertilitylikepprgene
AT arnalnadege caseofgenefragmentationinplantmitochondriafixedbytheselectionofacompensatoryrestoreroffertilitylikepprgene
AT balzerguesandrine caseofgenefragmentationinplantmitochondriafixedbytheselectionofacompensatoryrestoreroffertilitylikepprgene
AT benamarabdelilah caseofgenefragmentationinplantmitochondriafixedbytheselectionofacompensatoryrestoreroffertilitylikepprgene
AT bertinpierre caseofgenefragmentationinplantmitochondriafixedbytheselectionofacompensatoryrestoreroffertilitylikepprgene
AT brunaudveronique caseofgenefragmentationinplantmitochondriafixedbytheselectionofacompensatoryrestoreroffertilitylikepprgene
AT dargelgraffinceline caseofgenefragmentationinplantmitochondriafixedbytheselectionofacompensatoryrestoreroffertilitylikepprgene
AT machereldavid caseofgenefragmentationinplantmitochondriafixedbytheselectionofacompensatoryrestoreroffertilitylikepprgene
AT martinmagniettemarielaure caseofgenefragmentationinplantmitochondriafixedbytheselectionofacompensatoryrestoreroffertilitylikepprgene
AT quadradomartine caseofgenefragmentationinplantmitochondriafixedbytheselectionofacompensatoryrestoreroffertilitylikepprgene
AT namyolivier caseofgenefragmentationinplantmitochondriafixedbytheselectionofacompensatoryrestoreroffertilitylikepprgene
AT mireauhakim caseofgenefragmentationinplantmitochondriafixedbytheselectionofacompensatoryrestoreroffertilitylikepprgene