Initial sequence and comparative analysis of the cat genome

Joan Pontius(Science Applications International Corporation (United States)), James C. Mullikin(National Human Genome Research Institute), Douglas R. Smith, Agencourt Sequencing Team(Broad Institute), Kerstin Lindblad‐Toh(Broad Institute), Sante Gnerre(Broad Institute), Michèle Clamp(Broad Institute), Jean L. Chang(Broad Institute), Robert D. Stephens(Science Applications International Corporation (United States)), Beena Neelam(Science Applications International Corporation (United States)), Natalia Volfovsky(National Institutes of Health), Alejandro A. Schäffer(National Institutes of Health), Richa Agarwala(National Center for Biotechnology Information), Kristina Narfström(University of Missouri), William J. Murphy(University of Pennsylvania), Urs Giger(University of Pennsylvania), Alfred L. Roca(Universidade do Porto), Agostinho Antunes(Universidade do Porto), Marilyn Menotti‐Raymond(National Cancer Institute), Naoya Yuhki(National Cancer Institute), Jill Pecon‐Slattery(National Cancer Institute), Warren E. Johnson(National Cancer Institute), Guillaume Bourque(University of California San Diego), Glenn Tesler(University of California San Diego), NISC Comparative Sequencing Program, Stephen J. O’Brien(National Cancer Institute)
Genome Research
November 1, 2007
Cited by 377Open Access
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Abstract

The genome sequence (1.9-fold coverage) of an inbred Abyssinian domestic cat was assembled, mapped, and annotated with a comparative approach that involved cross-reference to annotated genome assemblies of six mammals (human, chimpanzee, mouse, rat, dog, and cow). The results resolved chromosomal positions for 663,480 contigs, 20,285 putative feline gene orthologs, and 133,499 conserved sequence blocks (CSBs). Additional annotated features include repetitive elements, endogenous retroviral sequences, nuclear mitochondrial (numt) sequences, micro-RNAs, and evolutionary breakpoints that suggest historic balancing of translocation and inversion incidences in distinct mammalian lineages. Large numbers of single nucleotide polymorphisms (SNPs), deletion insertion polymorphisms (DIPs), and short tandem repeats (STRs), suitable for linkage or association studies were characterized in the context of long stretches of chromosome homozygosity. In spite of the light coverage capturing approximately 65% of euchromatin sequence from the cat genome, these comparative insights shed new light on the tempo and mode of gene/genome evolution in mammals, promise several research applications for the cat, and also illustrate that a comparative approach using more deeply covered mammals provides an informative, preliminary annotation of a light (1.9-fold) coverage mammal genome sequence.


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