bioRxivEvolutionary Biology
Haplotype divergence supports ancient asexuality in the oribatid mite Oppiella nova
A. Brandt, P. Tran Van, C. Bluhm, Y. Anselmetti, Z. Dumas, E. Figuet, C. M. Francois, N. Galtier, B. Heimburger, K. S. Jaron, M. Labedan, M. Maraun, D. J. Parker, M. Robinson-Rechavi, I. Schaefer, P. Simion, S. Scheu, T. Schwander, J. Bast
Abstract
Sex strongly impacts genome evolution via recombination and segregation. In the absence of these processes, haplotypes within lineages of diploid organisms are predicted to accumulate mutations independently of each other and diverge over time. This so-called Meselson effect is regarded as a strong indicator of the long-term evolution under obligate asexuality. Here, we present genomic and transcriptomic data of three populations of the asexual oribatid mite species Oppiella nova and its sexual relative Oppiella subpectinata. We document strikingly different patterns of haplotype divergence between the two species, strongly supporting Meselson effect like evolution and ancient asexuality in O. nova: (I) Variation within individuals exceeds variation between populations in O. nova but vice versa in O. subpectinata. (II) Two O. nova sub-lineages feature a high proportion of heterozygous genotypes and lineage-specific haplotypes, indicating that haplotypes diverged independently within the two lineages after their split. (III) The deepest split in gene trees generally separates haplotypes in O. nova, but populations in O. subpectinata. (IV) Tree topologies of the two haplotypes match each other. Our findings provide positive evidence for the absence of sex over evolutionary time in O. nova and suggest that asexual oribatid mites can escape the dead-end fate usually associated with asexual lineages.
- organism: mouse
- assay: whole-genome sequencing
- assay: bulk RNA-seq
- research focus: chromatin & epigenetic regulation
- research focus: development & morphogenesis
- research focus: cell type annotation
- research focus: clustering
- approach: statistical model
- approach: genetic perturbation / CRISPR
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