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Please use this identifier to cite or link to this item:
http://hdl.handle.net/10174/41386
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| Title: | The Pecari tajacu genome: A tool for its conservation and the study of the Suoidea superfamily |
| Authors: | Amaral, AJ Eory, L Santos, D Toral, FLB Delgado, I Leitão, A Gama, LT Archibald, AL |
| Keywords: | Pecary de novo sequencing |
| Issue Date: | 21-Jul-2025 |
| Citation: | A. J. Amaral, L. Eory, D. Santos, F. L. B. Toral, I. Delgado, A. Leitão, L. T. Gama, and A. L. Archibald (2025) The Pecari tajacu genome: A tool for its conservation and
the study of the Suoidea superfamily. 40th International Society for Animal Genetics Conference, ISAG. Daejeon, Republic of Korea, July 20-25 2025. |
| Abstract: | The goal of this study is the development of a high-quality assembly
for the Pecari tajacu species. The Suoidea superfamily groups
2 families: Suidae and Tayassuidae. Suidae species inhabit Africa and
Eurasia, occupying a wide range of habitats. The same applies to the
Tayassuidae species that live in the Americas and were the first from
Suoidea to diverge from their common ancestor in North America ~36
Ma. Lineages of Tayassuidae from South America diverged around 10
Ma. Divergence between peccary genera is estimated as early as the late Myocene. Tayassu pecari and Catagonus wagneri are more closely related
to each other than to Pecari tajacu. Despite their significance, the
genomes of the Tayassuidae family remain poorly characterized. Their
conservation status ranges from least concern (P. tajacu), to vulnerable
(T. pecari), to endangered (C. wagneri). Developing high-quality reference
genomes is essential for the understanding of the evolution and
genetics of these species and for enhancing conservation efforts. Blood
samples were collected from a female zoo specimen and flash-frozen in
liquid nitrogen. High molecular weight DNA was isolated for Oxford
Nanopore (100×) and PacBio HiFi sequencing (70×), alongside Dovetail
Omni-C data generation. Assembly and scaffolding of nanopore
reads was performed using a pipeline that included canu-medata-salsa2.
Assembly and scaffolding of Hi-Fi reads was performed using hifiasm
and yahs. The HiFi assembly achieved higher contiguity (N50: 121
Mbp) and lower error rate then the Nanopore assembly (N50: 46 Mpb).
The HiFi assembly reconstructed both pseudo haplotypes at chromosome
level, whereas the Nanopore data yielded a close to chromosome
level single pseudo-haplotype assembly. Comparative analysis of the P.
tajacu and the S. scrofa genome (Sscrofa11.1) confirmed that the chromosome
level assemblies are consistent with expected homology based
on previous ZOO-FISH analyses. This high-quality, haplotype-resolved
reference genome offers a robust framework for further studies regarding
the species genetic structure and diversity. |
| URI: | http://hdl.handle.net/10174/41386 |
| Type: | lecture |
| Appears in Collections: | ZOO - Comunicações - Em Congressos Científicos Internacionais
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