Low Mutation Load in a Supergene Underpinning Alternative Male Mating Strategies in Ruff (Calidris pugnax)

Author:

Hill Jason1ORCID,Enbody Erik D12ORCID,Bi Huijuan1,Lamichhaney Sangeet13,Lei Weipan4,Chen Juexin5,Wei Chentao5,Liu Yang5ORCID,Schwochow Doreen6,Younis Shady17,Widemo Fredrik8,Andersson Leif19ORCID

Affiliation:

1. Department of Medical Biochemistry and Microbiology, Uppsala University , SE-75123 Uppsala , Sweden

2. Department of Biomolecular Engineering, University of California Santa Cruz , Santa Cruz, CA 95060 , USA

3. Department of Biological Sciences, Kent State University , Kent, OH 44241 , USA

4. Key Laboratory for Biodiversity Science and Ecological Engineering, National Demonstration Center for Experimental Life Sciences and Biotechnology Education, College of Life Sciences, Beijing Normal University , 100875 Beijing , China

5. State Key Laboratory of Biocontrol, School of Ecology, Sun Yat-sen University , 510275 Guangzhou , China

6. Department of Animal Breeding and Genetics, Swedish University of Agricultural Sciences , SE-75007 Uppsala , Sweden

7. Division of Immunology and Rheumatology, School of Medicine, Stanford University , Stanford, CA 94305 , USA

8. Department of Wildlife, Fish and Environmental Studies, Swedish University of Agricultural Sciences , SE-901 83 Umeå , Sweden

9. Department of Veterinary Integrative Biosciences, Texas A&M University , College Station, TX 77843 , USA

Abstract

Abstract A paradox in evolutionary biology is how supergenes can maintain high fitness despite reduced effective population size, the suppression of recombination, and the expected accumulation of mutational load. The ruff supergene involves 2 rare inversion haplotypes (satellite and faeder). These are recessive lethals but with dominant effects on male mating strategies, plumage, and body size. Sequence divergence to the wild-type (independent) haplotype indicates that the inversion could be as old as 4 million years. Here, we have constructed a highly contiguous genome assembly of the inversion region for both the independent and satellite haplotypes. Based on the new data, we estimate that the recombination event(s) creating the satellite haplotype occurred only about 70,000 yr ago. Contrary to expectations for supergenes, we find no substantial expansion of repeats and only a modest mutation load on the satellite and faeder haplotypes despite high sequence divergence to the non-inverted haplotype (1.46%). The essential centromere protein N (CENPN) gene is disrupted by the inversion and is as well conserved on the inversion haplotypes as on the noninversion haplotype. These results suggest that the inversion may be much younger than previously thought. The low mutation load, despite recessive lethality, may be explained by the introgression of the inversion from a now extinct lineage.

Publisher

Oxford University Press (OUP)

Subject

Genetics,Molecular Biology,Ecology, Evolution, Behavior and Systematics

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