Cargando…

Chromatin landscape associated with sexual differentiation in a UV sex determination system

In many eukaryotes, such as dioicous mosses and many algae, sex is determined by UV sex chromosomes and is expressed during the haploid phase of the life cycle. In these species, the male and female developmental programs are initiated by the presence of the U- or V-specific regions of the sex chrom...

Descripción completa

Detalles Bibliográficos
Autores principales: Gueno, Josselin, Borg, Michael, Bourdareau, Simon, Cossard, Guillaume, Godfroy, Olivier, Lipinska, Agnieszka, Tirichine, Leila, Cock, J Mark, Coelho, Susana M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8989524/
https://www.ncbi.nlm.nih.gov/pubmed/35253891
http://dx.doi.org/10.1093/nar/gkac145
_version_ 1784683193353371648
author Gueno, Josselin
Borg, Michael
Bourdareau, Simon
Cossard, Guillaume
Godfroy, Olivier
Lipinska, Agnieszka
Tirichine, Leila
Cock, J Mark
Coelho, Susana M
author_facet Gueno, Josselin
Borg, Michael
Bourdareau, Simon
Cossard, Guillaume
Godfroy, Olivier
Lipinska, Agnieszka
Tirichine, Leila
Cock, J Mark
Coelho, Susana M
author_sort Gueno, Josselin
collection PubMed
description In many eukaryotes, such as dioicous mosses and many algae, sex is determined by UV sex chromosomes and is expressed during the haploid phase of the life cycle. In these species, the male and female developmental programs are initiated by the presence of the U- or V-specific regions of the sex chromosomes but, as in XY and ZW systems, sexual differentiation is largely driven by autosomal sex-biased gene expression. The mechanisms underlying the regulation of sex-biased expression of genes during sexual differentiation remain elusive. Here, we investigated the extent and nature of epigenomic changes associated with UV sexual differentiation in the brown alga Ectocarpus, a model UV system. Six histone modifications were quantified in near-isogenic lines, leading to the identification of 16 chromatin signatures across the genome. Chromatin signatures correlated with levels of gene expression and histone PTMs changes in males versus females occurred preferentially at genes involved in sex-specific pathways. Despite the absence of chromosome scale dosage compensation and the fact that UV sex chromosomes recombine across most of their length, the chromatin landscape of these chromosomes was remarkably different to that of autosomes. Hotspots of evolutionary young genes in the pseudoautosomal regions appear to drive the exceptional chromatin features of UV sex chromosomes.
format Online
Article
Text
id pubmed-8989524
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-89895242022-04-08 Chromatin landscape associated with sexual differentiation in a UV sex determination system Gueno, Josselin Borg, Michael Bourdareau, Simon Cossard, Guillaume Godfroy, Olivier Lipinska, Agnieszka Tirichine, Leila Cock, J Mark Coelho, Susana M Nucleic Acids Res Gene regulation, Chromatin and Epigenetics In many eukaryotes, such as dioicous mosses and many algae, sex is determined by UV sex chromosomes and is expressed during the haploid phase of the life cycle. In these species, the male and female developmental programs are initiated by the presence of the U- or V-specific regions of the sex chromosomes but, as in XY and ZW systems, sexual differentiation is largely driven by autosomal sex-biased gene expression. The mechanisms underlying the regulation of sex-biased expression of genes during sexual differentiation remain elusive. Here, we investigated the extent and nature of epigenomic changes associated with UV sexual differentiation in the brown alga Ectocarpus, a model UV system. Six histone modifications were quantified in near-isogenic lines, leading to the identification of 16 chromatin signatures across the genome. Chromatin signatures correlated with levels of gene expression and histone PTMs changes in males versus females occurred preferentially at genes involved in sex-specific pathways. Despite the absence of chromosome scale dosage compensation and the fact that UV sex chromosomes recombine across most of their length, the chromatin landscape of these chromosomes was remarkably different to that of autosomes. Hotspots of evolutionary young genes in the pseudoautosomal regions appear to drive the exceptional chromatin features of UV sex chromosomes. Oxford University Press 2022-03-07 /pmc/articles/PMC8989524/ /pubmed/35253891 http://dx.doi.org/10.1093/nar/gkac145 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of Nucleic Acids Research. 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 Gene regulation, Chromatin and Epigenetics
Gueno, Josselin
Borg, Michael
Bourdareau, Simon
Cossard, Guillaume
Godfroy, Olivier
Lipinska, Agnieszka
Tirichine, Leila
Cock, J Mark
Coelho, Susana M
Chromatin landscape associated with sexual differentiation in a UV sex determination system
title Chromatin landscape associated with sexual differentiation in a UV sex determination system
title_full Chromatin landscape associated with sexual differentiation in a UV sex determination system
title_fullStr Chromatin landscape associated with sexual differentiation in a UV sex determination system
title_full_unstemmed Chromatin landscape associated with sexual differentiation in a UV sex determination system
title_short Chromatin landscape associated with sexual differentiation in a UV sex determination system
title_sort chromatin landscape associated with sexual differentiation in a uv sex determination system
topic Gene regulation, Chromatin and Epigenetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8989524/
https://www.ncbi.nlm.nih.gov/pubmed/35253891
http://dx.doi.org/10.1093/nar/gkac145
work_keys_str_mv AT guenojosselin chromatinlandscapeassociatedwithsexualdifferentiationinauvsexdeterminationsystem
AT borgmichael chromatinlandscapeassociatedwithsexualdifferentiationinauvsexdeterminationsystem
AT bourdareausimon chromatinlandscapeassociatedwithsexualdifferentiationinauvsexdeterminationsystem
AT cossardguillaume chromatinlandscapeassociatedwithsexualdifferentiationinauvsexdeterminationsystem
AT godfroyolivier chromatinlandscapeassociatedwithsexualdifferentiationinauvsexdeterminationsystem
AT lipinskaagnieszka chromatinlandscapeassociatedwithsexualdifferentiationinauvsexdeterminationsystem
AT tirichineleila chromatinlandscapeassociatedwithsexualdifferentiationinauvsexdeterminationsystem
AT cockjmark chromatinlandscapeassociatedwithsexualdifferentiationinauvsexdeterminationsystem
AT coelhosusanam chromatinlandscapeassociatedwithsexualdifferentiationinauvsexdeterminationsystem