Cargando…
An Ancestral Balanced Inversion Polymorphism Confers Global Adaptation
Since the pioneering work of Dobzhansky in the 1930s and 1940s, many chromosomal inversions have been identified, but how they contribute to adaptation remains poorly understood. In Drosophila melanogaster, the widespread inversion polymorphism In(3R)Payne underpins latitudinal clines in fitness tra...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10234209/ https://www.ncbi.nlm.nih.gov/pubmed/37220650 http://dx.doi.org/10.1093/molbev/msad118 |
_version_ | 1785052435605094400 |
---|---|
author | Kapun, Martin Mitchell, Esra Durmaz Kawecki, Tadeusz J Schmidt, Paul Flatt, Thomas |
author_facet | Kapun, Martin Mitchell, Esra Durmaz Kawecki, Tadeusz J Schmidt, Paul Flatt, Thomas |
author_sort | Kapun, Martin |
collection | PubMed |
description | Since the pioneering work of Dobzhansky in the 1930s and 1940s, many chromosomal inversions have been identified, but how they contribute to adaptation remains poorly understood. In Drosophila melanogaster, the widespread inversion polymorphism In(3R)Payne underpins latitudinal clines in fitness traits on multiple continents. Here, we use single-individual whole-genome sequencing, transcriptomics, and published sequencing data to study the population genomics of this inversion on four continents: in its ancestral African range and in derived populations in Europe, North America, and Australia. Our results confirm that this inversion originated in sub-Saharan Africa and subsequently became cosmopolitan; we observe marked monophyletic divergence of inverted and noninverted karyotypes, with some substructure among inverted chromosomes between continents. Despite divergent evolution of this inversion since its out-of-Africa migration, derived non-African populations exhibit similar patterns of long-range linkage disequilibrium between the inversion breakpoints and major peaks of divergence in its center, consistent with balancing selection and suggesting that the inversion harbors alleles that are maintained by selection on several continents. Using RNA-sequencing, we identify overlap between inversion-linked single-nucleotide polymorphisms and loci that are differentially expressed between inverted and noninverted chromosomes. Expression levels are higher for inverted chromosomes at low temperature, suggesting loss of buffering or compensatory plasticity and consistent with higher inversion frequency in warm climates. Our results suggest that this ancestrally tropical balanced polymorphism spread around the world and became latitudinally assorted along similar but independent climatic gradients, always being frequent in subtropical/tropical areas but rare or absent in temperate climates. |
format | Online Article Text |
id | pubmed-10234209 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-102342092023-06-02 An Ancestral Balanced Inversion Polymorphism Confers Global Adaptation Kapun, Martin Mitchell, Esra Durmaz Kawecki, Tadeusz J Schmidt, Paul Flatt, Thomas Mol Biol Evol Discoveries Since the pioneering work of Dobzhansky in the 1930s and 1940s, many chromosomal inversions have been identified, but how they contribute to adaptation remains poorly understood. In Drosophila melanogaster, the widespread inversion polymorphism In(3R)Payne underpins latitudinal clines in fitness traits on multiple continents. Here, we use single-individual whole-genome sequencing, transcriptomics, and published sequencing data to study the population genomics of this inversion on four continents: in its ancestral African range and in derived populations in Europe, North America, and Australia. Our results confirm that this inversion originated in sub-Saharan Africa and subsequently became cosmopolitan; we observe marked monophyletic divergence of inverted and noninverted karyotypes, with some substructure among inverted chromosomes between continents. Despite divergent evolution of this inversion since its out-of-Africa migration, derived non-African populations exhibit similar patterns of long-range linkage disequilibrium between the inversion breakpoints and major peaks of divergence in its center, consistent with balancing selection and suggesting that the inversion harbors alleles that are maintained by selection on several continents. Using RNA-sequencing, we identify overlap between inversion-linked single-nucleotide polymorphisms and loci that are differentially expressed between inverted and noninverted chromosomes. Expression levels are higher for inverted chromosomes at low temperature, suggesting loss of buffering or compensatory plasticity and consistent with higher inversion frequency in warm climates. Our results suggest that this ancestrally tropical balanced polymorphism spread around the world and became latitudinally assorted along similar but independent climatic gradients, always being frequent in subtropical/tropical areas but rare or absent in temperate climates. Oxford University Press 2023-05-23 /pmc/articles/PMC10234209/ /pubmed/37220650 http://dx.doi.org/10.1093/molbev/msad118 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of Society for Molecular Biology and Evolution. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Discoveries Kapun, Martin Mitchell, Esra Durmaz Kawecki, Tadeusz J Schmidt, Paul Flatt, Thomas An Ancestral Balanced Inversion Polymorphism Confers Global Adaptation |
title | An Ancestral Balanced Inversion Polymorphism Confers Global Adaptation |
title_full | An Ancestral Balanced Inversion Polymorphism Confers Global Adaptation |
title_fullStr | An Ancestral Balanced Inversion Polymorphism Confers Global Adaptation |
title_full_unstemmed | An Ancestral Balanced Inversion Polymorphism Confers Global Adaptation |
title_short | An Ancestral Balanced Inversion Polymorphism Confers Global Adaptation |
title_sort | ancestral balanced inversion polymorphism confers global adaptation |
topic | Discoveries |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10234209/ https://www.ncbi.nlm.nih.gov/pubmed/37220650 http://dx.doi.org/10.1093/molbev/msad118 |
work_keys_str_mv | AT kapunmartin anancestralbalancedinversionpolymorphismconfersglobaladaptation AT mitchellesradurmaz anancestralbalancedinversionpolymorphismconfersglobaladaptation AT kaweckitadeuszj anancestralbalancedinversionpolymorphismconfersglobaladaptation AT schmidtpaul anancestralbalancedinversionpolymorphismconfersglobaladaptation AT flattthomas anancestralbalancedinversionpolymorphismconfersglobaladaptation AT kapunmartin ancestralbalancedinversionpolymorphismconfersglobaladaptation AT mitchellesradurmaz ancestralbalancedinversionpolymorphismconfersglobaladaptation AT kaweckitadeuszj ancestralbalancedinversionpolymorphismconfersglobaladaptation AT schmidtpaul ancestralbalancedinversionpolymorphismconfersglobaladaptation AT flattthomas ancestralbalancedinversionpolymorphismconfersglobaladaptation |