The draft genome of the Wisconsin Miniature SwineTM, a valuable biomedical research tool

Porcine biomedical models have emerged as valuable tools in biomedical research due to their physiological, anatomical, metabolic, immunological, and genetic similarities to humans. As a result, they offer greater relevance for translational studies than rodent models. Moreover, compared to nonhuman primates, porcine models are more cost-effective, easier to manipulate genetically, and raise fewer ethical concerns. However, the conventional breeds of swine most commonly used in research have rapid growth rates, which lead to logistical challenges such as increased space requirements, making them impractical as biomedical models. The Wisconsin Miniature SwineTM (WMSTM) was developed to address these shortcomings. The WMSTM porcine model grows slower, reaching and maintaining human sizes at adulthood. The model was also specifically designed to possess more human-like physiology that allows for easy modeling of comorbidities like obesity and metabolic syndrome that affect a large portion of the human population affected by chronic diseases. Thus, WMS™ is an ideal porcine gene editing platform for modeling complex multifactorial diseases. Here, we present the first draft genome assembly representative of the WMSTM line. The primary assembly was generated with ∼20× coverage of long reads from Oxford Nanopore Technologies and independently error-corrected using 23× Pacific Biosciences reads. Arima Genomics Hi-C data were used to improve contiguity. Largely congruent with the existing Sus scrofa genome, we also show the utility of WMSTM as a model through comparisons between 2 WMSTM genes and human homologs. Finally, we show the utility of genotyping by sequencing across WMSTM herds. The WMSTM genome generated here is highly complete and supports investigators utilizing WMSTM in biomedical research.

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Publication Details

Journal
G3 Genes Genomes Genetics
Published
2025-04-07
DOI
https://doi.org/10.1093/g3journal/jkaf067
Citations
4
Primary Topic
Molecular Biology Techniques and Applications
Type
article
Field-Weighted Citation Impact
3.22

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article

The draft genome of the Wisconsin Miniature SwineTM, a valuable biomedical research tool

C. Dustin Rubinstein, Christopher A. Bradfield, Jennifer J. Meudt, Molly J. Zeller et al.
4 citations
G3 Genes Genomes Genetics
Molecular Biology Techniques and Applications
3.22
article

The draft genome of the Wisconsin Miniature SwineTM, a valuable biomedical research tool

C. Dustin Rubinstein, Christopher A. Bradfield, Jennifer J. Meudt, Molly J. Zeller, Alex Veith, Charles M. Konsitzke, Joshua Hyman, Mark E. Berres, Dhanansayan Shanmuganayagam, Derek M. Pavelec, James M. Speers, Taeyoung Shin, Jennifer M. Frank, Jamie L. Reichert, Bridget Ladell
article en
4 citations

Abstract

Porcine biomedical models have emerged as valuable tools in biomedical research due to their physiological, anatomical, metabolic, immunological, and genetic similarities to humans. As a result, they offer greater relevance for translational studies than rodent models. Moreover, compared to nonhuman primates, porcine models are more cost-effective, easier to manipulate genetically, and raise fewer ethical concerns. However, the conventional breeds of swine most commonly used in research have rapid growth rates, which lead to logistical challenges such as increased space requirements, making them impractical as biomedical models. The Wisconsin Miniature SwineTM (WMSTM) was developed to address these shortcomings. The WMSTM porcine model grows slower, reaching and maintaining human sizes at adulthood. The model was also specifically designed to possess more human-like physiology that allows for easy modeling of comorbidities like obesity and metabolic syndrome that affect a large portion of the human population affected by chronic diseases. Thus, WMS™ is an ideal porcine gene editing platform for modeling complex multifactorial diseases. Here, we present the first draft genome assembly representative of the WMSTM line. The primary assembly was generated with ∼20× coverage of long reads from Oxford Nanopore Technologies and independently error-corrected using 23× Pacific Biosciences reads. Arima Genomics Hi-C data were used to improve contiguity. Largely congruent with the existing Sus scrofa genome, we also show the utility of WMSTM as a model through comparisons between 2 WMSTM genes and human homologs. Finally, we show the utility of genotyping by sequencing across WMSTM herds. The WMSTM genome generated here is highly complete and supports investigators utilizing WMSTM in biomedical research.

G3 Genes Genomes GeneticsVol. 15(6)
University of Wisconsin System (US), University of Wisconsin–Madison (US)
University of Wisconsin-Madison, University of Wisconsin Carbone Cancer Center, National Institutes of Health, National Cancer Institute, National Institute of Environmental Health Sciences
Good health and well-being
Openalex Percentile: Top 9%
Molecular Biology Techniques and Applications
3.22
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