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Genome assembly of the basket willow, Salix viminalis, reveals earliest stages of sex chromosome expansion
BACKGROUND: Sex chromosomes have evolved independently multiple times in eukaryotes and are therefore considered a prime example of convergent genome evolution. Sex chromosomes are known to emerge after recombination is halted between a homologous pair of chromosomes, and this leads to a range of no...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7329446/ https://www.ncbi.nlm.nih.gov/pubmed/32605573 http://dx.doi.org/10.1186/s12915-020-00808-1 |
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author | Almeida, Pedro Proux-Wera, Estelle Churcher, Allison Soler, Lucile Dainat, Jacques Pucholt, Pascal Nordlund, Jessica Martin, Tom Rönnberg-Wästljung, Ann-Christin Nystedt, Björn Berlin, Sofia Mank, Judith E. |
author_facet | Almeida, Pedro Proux-Wera, Estelle Churcher, Allison Soler, Lucile Dainat, Jacques Pucholt, Pascal Nordlund, Jessica Martin, Tom Rönnberg-Wästljung, Ann-Christin Nystedt, Björn Berlin, Sofia Mank, Judith E. |
author_sort | Almeida, Pedro |
collection | PubMed |
description | BACKGROUND: Sex chromosomes have evolved independently multiple times in eukaryotes and are therefore considered a prime example of convergent genome evolution. Sex chromosomes are known to emerge after recombination is halted between a homologous pair of chromosomes, and this leads to a range of non-adaptive modifications causing gradual degeneration and gene loss on the sex-limited chromosome. However, the proximal causes of recombination suppression and the pace at which degeneration subsequently occurs remain unclear. RESULTS: Here, we use long- and short-read single-molecule sequencing approaches to assemble and annotate a draft genome of the basket willow, Salix viminalis, a species with a female heterogametic system at the earliest stages of sex chromosome emergence. Our single-molecule approach allowed us to phase the emerging Z and W haplotypes in a female, and we detected very low levels of Z/W single-nucleotide divergence in the non-recombining region. Linked-read sequencing of the same female and an additional male (ZZ) revealed the presence of two evolutionary strata supported by both divergence between the Z and W haplotypes and by haplotype phylogenetic trees. Gene order is still largely conserved between the Z and W homologs, although the W-linked region contains genes involved in cytokinin signaling regulation that are not syntenic with the Z homolog. Furthermore, we find no support across multiple lines of evidence for inversions, which have long been assumed to halt recombination between the sex chromosomes. CONCLUSIONS: Our data suggest that selection against recombination is a more gradual process at the earliest stages of sex chromosome formation than would be expected from an inversion and may result instead from the accumulation of transposable elements. Our results present a cohesive understanding of the earliest genomic consequences of recombination suppression as well as valuable insights into the initial stages of sex chromosome formation and regulation of sex differentiation. |
format | Online Article Text |
id | pubmed-7329446 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-73294462020-07-02 Genome assembly of the basket willow, Salix viminalis, reveals earliest stages of sex chromosome expansion Almeida, Pedro Proux-Wera, Estelle Churcher, Allison Soler, Lucile Dainat, Jacques Pucholt, Pascal Nordlund, Jessica Martin, Tom Rönnberg-Wästljung, Ann-Christin Nystedt, Björn Berlin, Sofia Mank, Judith E. BMC Biol Research Article BACKGROUND: Sex chromosomes have evolved independently multiple times in eukaryotes and are therefore considered a prime example of convergent genome evolution. Sex chromosomes are known to emerge after recombination is halted between a homologous pair of chromosomes, and this leads to a range of non-adaptive modifications causing gradual degeneration and gene loss on the sex-limited chromosome. However, the proximal causes of recombination suppression and the pace at which degeneration subsequently occurs remain unclear. RESULTS: Here, we use long- and short-read single-molecule sequencing approaches to assemble and annotate a draft genome of the basket willow, Salix viminalis, a species with a female heterogametic system at the earliest stages of sex chromosome emergence. Our single-molecule approach allowed us to phase the emerging Z and W haplotypes in a female, and we detected very low levels of Z/W single-nucleotide divergence in the non-recombining region. Linked-read sequencing of the same female and an additional male (ZZ) revealed the presence of two evolutionary strata supported by both divergence between the Z and W haplotypes and by haplotype phylogenetic trees. Gene order is still largely conserved between the Z and W homologs, although the W-linked region contains genes involved in cytokinin signaling regulation that are not syntenic with the Z homolog. Furthermore, we find no support across multiple lines of evidence for inversions, which have long been assumed to halt recombination between the sex chromosomes. CONCLUSIONS: Our data suggest that selection against recombination is a more gradual process at the earliest stages of sex chromosome formation than would be expected from an inversion and may result instead from the accumulation of transposable elements. Our results present a cohesive understanding of the earliest genomic consequences of recombination suppression as well as valuable insights into the initial stages of sex chromosome formation and regulation of sex differentiation. BioMed Central 2020-06-30 /pmc/articles/PMC7329446/ /pubmed/32605573 http://dx.doi.org/10.1186/s12915-020-00808-1 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Article Almeida, Pedro Proux-Wera, Estelle Churcher, Allison Soler, Lucile Dainat, Jacques Pucholt, Pascal Nordlund, Jessica Martin, Tom Rönnberg-Wästljung, Ann-Christin Nystedt, Björn Berlin, Sofia Mank, Judith E. Genome assembly of the basket willow, Salix viminalis, reveals earliest stages of sex chromosome expansion |
title | Genome assembly of the basket willow, Salix viminalis, reveals earliest stages of sex chromosome expansion |
title_full | Genome assembly of the basket willow, Salix viminalis, reveals earliest stages of sex chromosome expansion |
title_fullStr | Genome assembly of the basket willow, Salix viminalis, reveals earliest stages of sex chromosome expansion |
title_full_unstemmed | Genome assembly of the basket willow, Salix viminalis, reveals earliest stages of sex chromosome expansion |
title_short | Genome assembly of the basket willow, Salix viminalis, reveals earliest stages of sex chromosome expansion |
title_sort | genome assembly of the basket willow, salix viminalis, reveals earliest stages of sex chromosome expansion |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7329446/ https://www.ncbi.nlm.nih.gov/pubmed/32605573 http://dx.doi.org/10.1186/s12915-020-00808-1 |
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