A Chromosome-Length Reference Genome for the Endangered Pacific Pocket Mouse Reveals Recent Inbreeding in a Historically Large Population

Author:

Wilder Aryn P1ORCID,Dudchenko Olga23,Curry Caitlin1,Korody Marisa1,Turbek Sheela P14ORCID,Daly Mark5,Misuraca Ann1,Wang Gaojianyong6,Khan Ruqayya2,Weisz David2,Fronczek Julie1,Aiden Erez Lieberman23789,Houck Marlys L1,Shier Debra M110,Ryder Oliver A1ORCID,Steiner Cynthia C1

Affiliation:

1. Conservation Science Wildlife Health, San Diego Zoo Wildlife Alliance , Escondido, CA , USA

2. The Center for Genome Architecture, Department of Molecular and Human Genetics, Baylor College of Medicine , Houston, TX , USA

3. Center for Theoretical Biological Physics and Department of Computer Science, Rice University , Houston, TX , USA

4. Ecology and Evolutionary Biology, University of Colorado , Boulder, CO , USA

5. Dovetail Genomics , Scotts Valley, CA , USA

6. Department of Genome Regulation, Max Planck Institute for Molecular Genetics , Berlin , Germany

7. UWA School of Agriculture and Environment, The University of Western Australia , Crawley , Australia

8. Broad Institute of MIT and Harvard , Cambridge, MA , USA

9. Shanghai Institute for Advanced Immunochemical Studies , ShanghaiTech , China

10. Department of Ecology & Evolutionary Biology, University of California Los Angeles , Los Angeles, CA , USA

Abstract

Abstract High-quality reference genomes are fundamental tools for understanding population history, and can provide estimates of genetic and demographic parameters relevant to the conservation of biodiversity. The federally endangered Pacific pocket mouse (PPM), which persists in three small, isolated populations in southern California, is a promising model for studying how demographic history shapes genetic diversity, and how diversity in turn may influence extinction risk. To facilitate these studies in PPM, we combined PacBio HiFi long reads with Omni-C and Hi-C data to generate a de novo genome assembly, and annotated the genome using RNAseq. The assembly comprised 28 chromosome-length scaffolds (N50 = 72.6 MB) and the complete mitochondrial genome, and included a long heterochromatic region on chromosome 18 not represented in the previously available short-read assembly. Heterozygosity was highly variable across the genome of the reference individual, with 18% of windows falling in runs of homozygosity (ROH) >1 MB, and nearly 9% in tracts spanning >5 MB. Yet outside of ROH, heterozygosity was relatively high (0.0027), and historical Ne estimates were large. These patterns of genetic variation suggest recent inbreeding in a formerly large population. Currently the most contiguous assembly for a heteromyid rodent, this reference genome provides insight into the past and recent demographic history of the population, and will be a critical tool for management and future studies of outbreeding depression, inbreeding depression, and genetic load.

Funder

Morris Animal Foundation

DNA Zoo

Illumina, Inc

IBM

Pawsey Supercomputing Center

Welch Foundation

McNair Medical Institute

National Institutes of Health

US-Israel Binational Science Foundation

National Science Foundation

Publisher

Oxford University Press (OUP)

Subject

Genetics,Ecology, Evolution, Behavior and Systematics

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