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PMID: 33305796 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S.

Ultracontinuous Single Haplotype Genome Assemblies for the Domestic Cat (Felis catus) and Asian Leopard Cat (Prionailurus bengalensis).

The Journal of heredity ·Vol. 112 ·No. 2 ·2021-00-29 ·Pages 165-173

Bredemeyer KR, Harris AJ, Li G, Zhao L, Foley NM, Roelke-Parker M, O'Brien SJ, Lyons LA, Warren WC, Murphy WJ

Abstract

In addition to including one of the most popular companion animals, species from the cat family Felidae serve as a powerful system for genetic analysis of inherited and infectious disease, as well as for the study of phenotypic evolution and speciation. Previous diploid-based genome assemblies for the domestic cat have served as the primary reference for genomic studies within the cat family. However, these versions suffered from poor resolution of complex and highly repetitive regions, with substantial amounts of unplaced sequence that is polymorphic or copy number variable. We sequenced the genome of a female F1 Bengal hybrid cat, the offspring of a domestic cat (Felis catus) x Asian leopard cat (Prionailurus bengalensis) cross, with PacBio long sequence reads and used Illumina sequence reads from the parents to phase >99.9% of the reads into the 2 species' haplotypes. De novo assembly of the phased reads produced highly continuous haploid genome assemblies for the domestic cat and Asian leopard cat, with contig N50 statistics exceeding 83 Mb for both genomes. Whole-genome alignments reveal the Felis and Prionailurus genomes are colinear, and the cytogenetic differences between the homologous F1 and E4 chromosomes represent a case of centromere repositioning in the absence of a chromosomal inversion. Both assemblies offer significant improvements over the previous domestic cat reference genome, with a 100% increase in contiguity and the capture of the vast majority of chromosome arms in 1 or 2 large contigs. We further demonstrated that comparably accurate F1 haplotype phasing can be achieved with members of the same species when one or both parents of the trio are not available. These novel genome resources will empower studies of feline precision medicine, adaptation, and speciation.

Keywords
Felidae PacBio genome interspecies hybrid trio-binning
MeSH Terms
Animals Cats/genetics Chromosome Mapping Felidae/genetics Female Genome Haplotypes Hybridization, Genetic Male
Authors & Affiliations
10 authors, click to expand affiliations / ORCID
Bredemeyer Kevin R
Veterinary Integrative Biosciences, Texas A&M University, College Station, TX. | Interdisciplinary Program in Genetics, Texas A&M University, College Station, TX.
Harris Andrew J
Veterinary Integrative Biosciences, Texas A&M University, College Station, TX. | Interdisciplinary Program in Genetics, Texas A&M University, College Station, TX.
Li Gang
College of Life Sciences, Shaanxi Normal University, Xi'an, Shaanxi, China.
Zhao Le
College of Life Sciences, Shaanxi Normal University, Xi'an, Shaanxi, China.
Foley Nicole M
Veterinary Integrative Biosciences, Texas A&M University, College Station, TX.
Roelke-Parker Melody
Frederick National Laboratory of Cancer Research, Leidos Biomedical Research, Inc., Frederick, MD.
O'Brien Stephen J
Laboratory of Genomic Diversity-Center for Computer Technologies, ITMO University, Saint Petersburg, Russian Federation. | Guy Harvey Oceanographic Center, Nova Southeastern University, Fort Lauderdale, FL.
Lyons Leslie A
Department of Veterinary Medicine & Surgery, College of Veterinary Medicine, University of Missouri, Columbia, MO.
Warren Wesley C
Bond Life Science Center, University of Missouri, Columbia, MO.
Murphy William J
Veterinary Integrative Biosciences, Texas A&M University, College Station, TX. | Interdisciplinary Program in Genetics, Texas A&M University, College Station, TX.
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Article Info
Journal
The Journal of heredity
Abbr.
J Hered
ISSN
1465-7333
Published
2021-00-29
Pages
165-173
Language
English
Region
United States
NLM ID
0375373
PMCID
PMC8006817
Subset
IM
Grants
NIGMS NIH HHS · T32 GM135115 · United States
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