Genomes of Ellobius species provide insight into the evolutionary dynamics of mammalian sex chromosomes
- Eskeatnaf Mulugeta1,2,
- Evelyne Wassenaar1,
- Esther Sleddens-Linkels1,
- Wilfred F.J. van IJcken3,
- Edith Heard2,
- J. Anton Grootegoed1,
- Walter Just4,
- Joost Gribnau1 and
- Willy M. Baarends1
- 1Department of Developmental Biology, Erasmus MC, 3015CN, Rotterdam, The Netherlands;
- 2Institut Curie, Genetics and Developmental Biology Unit, 75248, Paris, France;
- 3Erasmus Center for Biomics, Erasmus MC, 3015CN, Rotterdam, The Netherlands;
- 4Institute of Human Genetics, University of Ulm, 89081, Ulm, Germany
- Corresponding author: w.baarends{at}erasmusmc.nl
Abstract
The X and Y sex chromosomes of placental mammals show hallmarks of a tumultuous evolutionary past. The X Chromosome has a rich and conserved gene content, while the Y Chromosome has lost most of its genes. In the Transcaucasian mole vole Ellobius lutescens, the Y Chromosome including Sry has been lost, and both females and males have a 17,X diploid karyotype. Similarly, the closely related Ellobius talpinus, has a 54,XX karyotype in both females and males. Here, we report the sequencing and assembly of the E. lutescens and E. talpinus genomes. The results indicate that the loss of the Y Chromosome in E. lutescens and E. talpinus occurred in two independent events. Four functional homologs of mouse Y-Chromosomal genes were detected in both female and male E. lutescens, of which three were also detected in the E. talpinus genome. One of these is Eif2s3y, known as the only Y-derived gene that is crucial for successful male meiosis. Female and male E. lutescens can carry one and the same X Chromosome with a largely conserved gene content, including all genes known to function in X Chromosome inactivation. The availability of the genomes of these mole vole species provides unique models to study the dynamics of sex chromosome evolution.
Footnotes
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[Supplemental material is available for this article.]
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Article published online before print. Article, supplemental material, and publication date are at http://www.genome.org/cgi/doi/10.1101/gr.201665.115.
- Received November 12, 2015.
- Accepted July 11, 2016.
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