4.2 Article

Sex chromosome differentiation via changes in the Y chromosome repeat landscape in African annual killifishes Nothobranchius furzeri and N. kadleci

期刊

CHROMOSOME RESEARCH
卷 30, 期 4, 页码 309-333

出版社

SPRINGER
DOI: 10.1007/s10577-022-09707-3

关键词

Inversion; Recombination suppression; Sex chromosome degeneration; Repeatome; RepeatExplorer; Sex chromosome polymorphism

资金

  1. Czech Science Foundation [19-22346Y]
  2. Deutsche Forschungsgemeinschaft [EN 280/15-1]
  3. Ministry of Education, Youth and Sports [CZ.02. 1.01/0.0/0.0/15_003/0000460 OP RDE]
  4. IAPG CAS, Libechov (Czech Academy of Sciences) [RVO:67985904]
  5. Charles University Research Centre program [204069]
  6. project e-Infrastruktura CZ [e-INFRA LM2018140]
  7. ELIXIR-CZ project [LM2018131]

向作者/读者索取更多资源

This study investigated the evolution of sex chromosomes in two sister species of African annual killifishes and found that both species shared homomorphic sex chromosomes that evolved prior to their divergence. The study also revealed differences in repetitive DNA sequences between the sex chromosomes, which may result from high turnover of repeat sequences and may not closely relate to the divergence inferred from earlier SNP analyses.
Homomorphic sex chromosomes and their turnover are common in teleosts. We investigated the evolution of nascent sex chromosomes in several populations of two sister species of African annual killifishes, Nothobranchius furzeri and N. kadleci, focusing on their under-studied repetitive landscape. We combined bioinformatic analyses of the repeatome with molecular cytogenetic techniques, including comparative genomic hybridization, fluorescence in situ hybridization with satellite sequences, ribosomal RNA genes (rDNA) and bacterial artificial chromosomes (BACs), and immunostaining of SYCP3 and MLH1 proteins to mark lateral elements of synaptonemal complexes and recombination sites, respectively. Both species share the same heteromorphic XY sex chromosome system, which thus evolved prior to their divergence. This was corroborated by sequence analysis of a putative master sex determining (MSD) gene gdf6Y in both species. Based on their divergence, differentiation of the XY sex chromosome pair started approximately 2 million years ago. In all populations, the gdf6Y gene mapped within a region rich in satellite DNA on the Y chromosome long arms. Despite their heteromorphism, X and Y chromosomes mostly pair regularly in meiosis, implying synaptic adjustment. In N. kadleci, Y-linked paracentric inversions like those previously reported in N. furzeri were detected. An inversion involving the MSD gene may suppress occasional recombination in the region, which we otherwise evidenced in the N. furzeri population MZCS-121 of the Limpopo clade lacking this inversion. Y chromosome centromeric repeats were reduced compared with the X chromosome and autosomes, which points to a role of relaxed meiotic drive in shaping the Y chromosome repeat landscape. We speculate that the recombination rate between sex chromosomes was reduced due to heterochiasmy. The observed differences between the repeat accumulations on the X and Y chromosomes probably result from high repeat turnover and may not relate closely to the divergence inferred from earlier SNP analyses.

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