1. Diversity of reptile sex chromosome evolution revealed by cytogenetic and linked-read sequencing
- Author
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Arthur Georges, Qi Zhou, Zexian Zhu, Foyez Shams, Tariq Ezaz, Stephen D. Sarre, Jason Dobry, Erik Wapstra, Jennifer A. Marshall Graves, Kazumi Matsubara, and Tony Gamble
- Subjects
Dosage compensation ,Autosome ,Evolutionary biology ,biology.animal ,Homologous chromosome ,Chromosome ,Vertebrate ,Chromosomal translocation ,Biology ,Gene ,Genome - Abstract
Reptile sex determination is attracting much attention because the great diversity of sex-determination and dosage compensation mechanisms permits us to approach fundamental questions about sex chromosome turnover and evolution. However, reptile sex chromosome variation remains largely uncharacterized and no reptile master sex determination genes have yet been identified. Here we describe a powerful and cost-effective “chromosomics” approach, combining probes generated from the microdissected sex chromosomes with transcriptome sequencing to explore this diversity in non-model Australian reptiles with heteromorphic or cryptic sex chromosomes. We tested the pipeline on a turtle, a gecko, and a worm-lizard, and we also identified sequences located on sex chromosomes in a monitor lizard using linked-read sequencing. Genes identified on sex chromosomes were compared to the chicken genome to identify homologous regions among the four species. We identified candidate sex determining genes within these regions, including conserved vertebrate sex-determining genes pdgfa, pdgfra amh and wt1, and demonstrated their testis or ovary-specific expression. All four species showed gene-by-gene rather than chromosome-wide dosage compensation. Our results imply that reptile sex chromosomes originated by independent acquisition of sex-determining genes on different autosomes, as well as translocations between different ancestral macro- and micro-chromosomes. We discuss the evolutionary drivers of the slow differentiation, but rapid turnover, of reptile sex chromosomes.
- Published
- 2021
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