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Contrasted histories of organelle and nuclear genomes underlying physiological diversification in a grass species
C(4) photosynthesis evolved multiple times independently in angiosperms, but most origins are relatively old so that the early events linked to photosynthetic diversification are blurred. The grass Alloteropsis semialata is an exception, as this species encompasses C(4) and non-C(4) populations. Usi...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7735283/ https://www.ncbi.nlm.nih.gov/pubmed/33171085 http://dx.doi.org/10.1098/rspb.2020.1960 |
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author | Bianconi, Matheus E. Dunning, Luke T. Curran, Emma V. Hidalgo, Oriane Powell, Robyn F. Mian, Sahr Leitch, Ilia J. Lundgren, Marjorie R. Manzi, Sophie Vorontsova, Maria S. Besnard, Guillaume Osborne, Colin P. Olofsson, Jill K. Christin, Pascal-Antoine |
author_facet | Bianconi, Matheus E. Dunning, Luke T. Curran, Emma V. Hidalgo, Oriane Powell, Robyn F. Mian, Sahr Leitch, Ilia J. Lundgren, Marjorie R. Manzi, Sophie Vorontsova, Maria S. Besnard, Guillaume Osborne, Colin P. Olofsson, Jill K. Christin, Pascal-Antoine |
author_sort | Bianconi, Matheus E. |
collection | PubMed |
description | C(4) photosynthesis evolved multiple times independently in angiosperms, but most origins are relatively old so that the early events linked to photosynthetic diversification are blurred. The grass Alloteropsis semialata is an exception, as this species encompasses C(4) and non-C(4) populations. Using phylogenomics and population genomics, we infer the history of dispersal and secondary gene flow before, during and after photosynthetic divergence in A. semialata. We further analyse the genome composition of individuals with varied ploidy levels to establish the origins of polyploids in this species. Detailed organelle phylogenies indicate limited seed dispersal within the mountainous region of origin and the emergence of a C(4) lineage after dispersal to warmer areas of lower elevation. Nuclear genome analyses highlight repeated secondary gene flow. In particular, the nuclear genome associated with the C(4) phenotype was swept into a distantly related maternal lineage probably via unidirectional pollen flow. Multiple intraspecific allopolyploidy events mediated additional secondary genetic exchanges between photosynthetic types. Overall, our results show that limited dispersal and isolation allowed lineage divergence, with photosynthetic innovation happening after migration to new environments, and pollen-mediated gene flow led to the rapid spread of the derived C(4) physiology away from its region of origin. |
format | Online Article Text |
id | pubmed-7735283 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-77352832020-12-28 Contrasted histories of organelle and nuclear genomes underlying physiological diversification in a grass species Bianconi, Matheus E. Dunning, Luke T. Curran, Emma V. Hidalgo, Oriane Powell, Robyn F. Mian, Sahr Leitch, Ilia J. Lundgren, Marjorie R. Manzi, Sophie Vorontsova, Maria S. Besnard, Guillaume Osborne, Colin P. Olofsson, Jill K. Christin, Pascal-Antoine Proc Biol Sci Evolution C(4) photosynthesis evolved multiple times independently in angiosperms, but most origins are relatively old so that the early events linked to photosynthetic diversification are blurred. The grass Alloteropsis semialata is an exception, as this species encompasses C(4) and non-C(4) populations. Using phylogenomics and population genomics, we infer the history of dispersal and secondary gene flow before, during and after photosynthetic divergence in A. semialata. We further analyse the genome composition of individuals with varied ploidy levels to establish the origins of polyploids in this species. Detailed organelle phylogenies indicate limited seed dispersal within the mountainous region of origin and the emergence of a C(4) lineage after dispersal to warmer areas of lower elevation. Nuclear genome analyses highlight repeated secondary gene flow. In particular, the nuclear genome associated with the C(4) phenotype was swept into a distantly related maternal lineage probably via unidirectional pollen flow. Multiple intraspecific allopolyploidy events mediated additional secondary genetic exchanges between photosynthetic types. Overall, our results show that limited dispersal and isolation allowed lineage divergence, with photosynthetic innovation happening after migration to new environments, and pollen-mediated gene flow led to the rapid spread of the derived C(4) physiology away from its region of origin. The Royal Society 2020-11-11 2020-11-11 /pmc/articles/PMC7735283/ /pubmed/33171085 http://dx.doi.org/10.1098/rspb.2020.1960 Text en © 2020 The Authors. http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/http://creativecommons.org/licenses/by/4.0/Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited. |
spellingShingle | Evolution Bianconi, Matheus E. Dunning, Luke T. Curran, Emma V. Hidalgo, Oriane Powell, Robyn F. Mian, Sahr Leitch, Ilia J. Lundgren, Marjorie R. Manzi, Sophie Vorontsova, Maria S. Besnard, Guillaume Osborne, Colin P. Olofsson, Jill K. Christin, Pascal-Antoine Contrasted histories of organelle and nuclear genomes underlying physiological diversification in a grass species |
title | Contrasted histories of organelle and nuclear genomes underlying physiological diversification in a grass species |
title_full | Contrasted histories of organelle and nuclear genomes underlying physiological diversification in a grass species |
title_fullStr | Contrasted histories of organelle and nuclear genomes underlying physiological diversification in a grass species |
title_full_unstemmed | Contrasted histories of organelle and nuclear genomes underlying physiological diversification in a grass species |
title_short | Contrasted histories of organelle and nuclear genomes underlying physiological diversification in a grass species |
title_sort | contrasted histories of organelle and nuclear genomes underlying physiological diversification in a grass species |
topic | Evolution |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7735283/ https://www.ncbi.nlm.nih.gov/pubmed/33171085 http://dx.doi.org/10.1098/rspb.2020.1960 |
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