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Possible stochastic sex determination in Bursaphelenchus nematodes

Sex determination mechanisms evolve surprisingly rapidly, yet little is known in the large nematode phylum other than for Caenorhabditis elegans, which relies on chromosomal XX-XO sex determination and a dosage compensation mechanism. Here we analyze by sex-specific genome sequencing and genetic ana...

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Autores principales: Shinya, Ryoji, Sun, Simo, Dayi, Mehmet, Tsai, Isheng Jason, Miyama, Atsushi, Chen, Anthony Fu, Hasegawa, Koichi, Antoshechkin, Igor, Kikuchi, Taisei, Sternberg, Paul W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9095866/
https://www.ncbi.nlm.nih.gov/pubmed/35546147
http://dx.doi.org/10.1038/s41467-022-30173-2
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author Shinya, Ryoji
Sun, Simo
Dayi, Mehmet
Tsai, Isheng Jason
Miyama, Atsushi
Chen, Anthony Fu
Hasegawa, Koichi
Antoshechkin, Igor
Kikuchi, Taisei
Sternberg, Paul W.
author_facet Shinya, Ryoji
Sun, Simo
Dayi, Mehmet
Tsai, Isheng Jason
Miyama, Atsushi
Chen, Anthony Fu
Hasegawa, Koichi
Antoshechkin, Igor
Kikuchi, Taisei
Sternberg, Paul W.
author_sort Shinya, Ryoji
collection PubMed
description Sex determination mechanisms evolve surprisingly rapidly, yet little is known in the large nematode phylum other than for Caenorhabditis elegans, which relies on chromosomal XX-XO sex determination and a dosage compensation mechanism. Here we analyze by sex-specific genome sequencing and genetic analysis sex determination in two fungal feeding/plant-parasitic Bursaphelenchus nematodes and find that their sex differentiation is more likely triggered by random, epigenetic regulation than by more well-known mechanisms of chromosomal or environmental sex determination. There is no detectable difference in male and female chromosomes, nor any linkage to sexual phenotype. Moreover, the protein sets of these nematodes lack genes involved in X chromosome dosage counting or compensation. By contrast, our genetic screen for sex differentiation mutants identifies a Bursaphelenchus ortholog of tra-1, the major output of the C. elegans sex determination cascade. Nematode sex determination pathways might have evolved by “bottom-up” accretion from the most downstream regulator, tra-1.
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spelling pubmed-90958662022-05-13 Possible stochastic sex determination in Bursaphelenchus nematodes Shinya, Ryoji Sun, Simo Dayi, Mehmet Tsai, Isheng Jason Miyama, Atsushi Chen, Anthony Fu Hasegawa, Koichi Antoshechkin, Igor Kikuchi, Taisei Sternberg, Paul W. Nat Commun Article Sex determination mechanisms evolve surprisingly rapidly, yet little is known in the large nematode phylum other than for Caenorhabditis elegans, which relies on chromosomal XX-XO sex determination and a dosage compensation mechanism. Here we analyze by sex-specific genome sequencing and genetic analysis sex determination in two fungal feeding/plant-parasitic Bursaphelenchus nematodes and find that their sex differentiation is more likely triggered by random, epigenetic regulation than by more well-known mechanisms of chromosomal or environmental sex determination. There is no detectable difference in male and female chromosomes, nor any linkage to sexual phenotype. Moreover, the protein sets of these nematodes lack genes involved in X chromosome dosage counting or compensation. By contrast, our genetic screen for sex differentiation mutants identifies a Bursaphelenchus ortholog of tra-1, the major output of the C. elegans sex determination cascade. Nematode sex determination pathways might have evolved by “bottom-up” accretion from the most downstream regulator, tra-1. Nature Publishing Group UK 2022-05-11 /pmc/articles/PMC9095866/ /pubmed/35546147 http://dx.doi.org/10.1038/s41467-022-30173-2 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Shinya, Ryoji
Sun, Simo
Dayi, Mehmet
Tsai, Isheng Jason
Miyama, Atsushi
Chen, Anthony Fu
Hasegawa, Koichi
Antoshechkin, Igor
Kikuchi, Taisei
Sternberg, Paul W.
Possible stochastic sex determination in Bursaphelenchus nematodes
title Possible stochastic sex determination in Bursaphelenchus nematodes
title_full Possible stochastic sex determination in Bursaphelenchus nematodes
title_fullStr Possible stochastic sex determination in Bursaphelenchus nematodes
title_full_unstemmed Possible stochastic sex determination in Bursaphelenchus nematodes
title_short Possible stochastic sex determination in Bursaphelenchus nematodes
title_sort possible stochastic sex determination in bursaphelenchus nematodes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9095866/
https://www.ncbi.nlm.nih.gov/pubmed/35546147
http://dx.doi.org/10.1038/s41467-022-30173-2
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