bioRxivZoologyPreprint
Leveraging whole genome sequencing to promote genetic diversity and population health in zoo-housed western lowland gorillas
J. Gorzynski, M. D. Danforth, V. Strong, I. Kutinsky, H. Murphy, L. Lowenstine, J. R. Priest, E. A. Ashley
Abstract
The sustainability of zoo populations is dependent on maintaining genetic diversity and controlling heritable disease. Here, we explore the integration of whole genome sequencing data in the management of the international zoological population of western lowland gorillas, focusing on genetic diversity and heritable diseases. By comparing kinship values derived from classical pedigree mapping and whole genome sequencing, we demonstrate that genomic data provides a more sensitive measure of relatedness. Our analysis reveals a decrease in genetic diversity due to closed breeding, emphasizing the potential for genetic intervention to mitigate negative impact on population fitness. We identify contributing factors to the decreasing genetic diversity including breeding within a closed population, unknown kinship among potential mates, and disproportionate genetic contributions from individual founders. Additionally, we highlight idiopathic myocardial fibrosis (IMF), a common cardiovascular pathology observed in zoologically housed gorillas, and identify a novel genetic variant in the TNNI3K gene that appears to be associated with this condition. These findings underscore the importance of incorporating molecular data into ex-situ population management strategies, and advocate for the adoption of advanced genomic techniques to optimize the genetic health and diversity of zoologically housed western lowland gorillas.
- organism: non-human primate
- assay: whole-genome sequencing
- research focus: genome assembly
- research focus: variant calling
- research focus: differential expression
- research focus: gene regulatory network inference
- approach: experimental assay
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