- Noh, Hyun Ji;
- Turner-Maier, Jason;
- Schulberg, S Anne;
- Fitzgerald, Michael L;
- Johnson, Jeremy;
- Allen, Kaitlin N;
- Hückstädt, Luis A;
- Batten, Annabelle J;
- Alfoldi, Jessica;
- Costa, Daniel P;
- Karlsson, Elinor K;
- Zapol, Warren M;
- Buys, Emmanuel S;
- Lindblad-Toh, Kerstin;
- Hindle, Allyson G
The Weddell seal (Leptonychotes weddellii) thrives in its extreme Antarctic environment. We generated the Weddell seal genome assembly and a high-quality annotation to investigate genome-wide evolutionary pressures that underlie its phenotype and to study genes implicated in hypoxia tolerance and a lipid-based metabolism. Genome-wide analyses included gene family expansion/contraction, positive selection, and diverged sequence (acceleration) compared to other placental mammals, identifying selection in coding and non-coding sequence in five pathways that may shape cardiovascular phenotype. Lipid metabolism as well as hypoxia genes contained more accelerated regions in the Weddell seal compared to genomic background. Top-significant genes were SUMO2 and EP300; both regulate hypoxia inducible factor signaling. Liver expression of four genes with the strongest acceleration signals differ between Weddell seals and a terrestrial mammal, sheep. We also report a high-density lipoprotein-like particle in Weddell seal serum not present in other mammals, including the shallow-diving harbor seal.