4.6 Article

Heterochiasmy and the establishment of gsdf as a novel sex determining gene in Atlantic halibut

期刊

PLOS GENETICS
卷 18, 期 2, 页码 -

出版社

PUBLIC LIBRARY SCIENCE
DOI: 10.1371/journal.pgen.1010011

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资金

  1. Sterling White Halibut
  2. Norwegian Ministry of Trade, Industry and Fisheries throughits funding of the Institute of Marine Research
  3. Swedish Research Council Formas [2012-00740, 2018-01008, 2017-00413, 2018-03017]
  4. [2018-04444]
  5. Swedish Research Council [2017-00413, 2018-03017] Funding Source: Swedish Research Council
  6. Forte [2012-00740] Funding Source: Forte
  7. Formas [2012-00740, 2018-01008, 2017-00413] Funding Source: Formas
  8. Vinnova [2018-01008] Funding Source: Vinnova

向作者/读者索取更多资源

This study reveals the sex chromosomes and sex determination mechanism of Atlantic halibut through genome sequencing analysis. The research found that male halibut have higher gene activity of the gonadal somatic cell derived factor gene, which is due to the enhanced function of mobile DNA sequences on the sex chromosomes. In addition, the study also found that the behavior of halibut chromosomes is similar to sex chromosomes, which may contribute to the rapid turnover of genetic sex determination systems in fish.
Atlantic Halibut (Hippoglossus hippoglossus) has a X/Y genetic sex determination system, but the sex determining factor is not known. We produced a high-quality genome assembly from a male and identified parts of chromosome 13 as the Y chromosome due to sequence divergence between sexes and segregation of sex genotypes in pedigrees. Linkage analysis revealed that all chromosomes exhibit heterochiasmy, i.e. male-only and female-only meiotic recombination regions (MRR/FRR). We show that FRR/MRR intervals differ in nucleotide diversity and repeat class content and that this is true also for other Pleuronectidae species. We further show that remnants of a Gypsy-like transposable element insertion on chr13 promotes early male specific expression of gonadal somatic cell derived factor (gsdf). Less than 4.5 MYA, this male-determining element evolved on an autosomal FRR segment featuring pre-existing male meiotic recombination barriers, thereby creating a Y chromosome. Our findings indicate that heterochiasmy may facilitate the evolution of genetic sex determination systems relying on linkage of sexually antagonistic loci to a sex-determining factor. Author summaryEven closely related fish species can have different sex chromosomes, but this turn-over of sex determination systems is poorly understood. Here, we used large-scale genome sequencing to determine the DNA sequence of the Atlantic halibut chromosomes and compared sequencing data from males and females to identify the sex chromosomes. We show that males have much higher gene activity of the gene gonadal somatic cell derived factor (gsdf), which is located on the sex chromosomes and has a role in testicular development. The genome contains many mobile DNA sequences, transposable elements (TEs), one placed in front of gsdf, enhancing its activity. This made gsdf the sex determining factor, thereby creating a new Y-chromosome. We further describe how all Atlantic halibut chromosomes behave similar to sex chromosomes in that most regions only recombine in one sex. This phenomenon may contribute to the rapid turn-over of genetic sex determination systems in fish. Our results highlight the molecular events creating a new Y-chromosome and show that the new Atlantic halibut Y was formed less than 4.5 million years ago. Future studies in Atlantic halibut and closely related species can shed light on mechanisms contributing to sex chromosome evolution in fish.

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