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Initial sequence and comparative analysis of the cat genome

  1. Author:
    Pontius, J. U.
    Mullikin, J. C.
    Smith, D. R.
    Lindblad-Toh, K.
    Gnerre, S.
    Clamp, M.
    Chang, J.
    Stephens, R.
    Neelam, B.
    Volfovsky, N.
    Schaffer, A. A.
    Agarwala, R.
    Narfstrom, K.
    Murphy, W. J.
    Giger, U.
    Roca, A. L.
    Antunes, A.
    Menotti-Raymond, M.
    Yuhki, N.
    Pecon-Slattery, J.
    Johnson, W. E.
    Bourque, G.
    Tesler, G.
    O'Brien, S. J.
    NISC Comparative Sequencing Program
  2. Author Address

    SAIC Frederick Inc, Lab Genom Divers, NCI Frederick, Frederick, MD 21702 USA. NHGRI, Comparat Genom Unit, Rockville, MD 20892 USA. Agencourt Biosci Corp, Beverly, MA 01915 USA. Broad Inst Harvard, Cambridge, MA 02141 USA. MIT, Cambridge, MA 02141 USA. SAIC Frederick Inc, Adv Biomed Comp Ctr, NCI Frederick, Frederick, MD 21702 USA. Natl Lib Med, NIH, Natl Ctr Biotechnol Informat, Bethesda, MD 20894 USA. Univ Missouri, Dept Vet Med & Surg, Dept Ophthalmol, Mason Eye Inst, Columbia, MO 65211 USA. Texas A&M Univ, Coll Vet Med & Biomed Sci, College Stn, TX 77843 USA. Univ Penn, Sch Vet Med, Med Genet Sect, Philadelphia, PA 19104 USA. NCI, Lab Genom Divers, Frederick, MD 21702 USA. Univ Porto, REQUIMTE, Dept Quim, Fac Ciencias, P-4169007 Oporto, Portugal. Univ Porto, CIMAR, Ctr Interdisciplinar Invest Marinha & Ambiental, P-4050123 Oporto, Portugal. Genome Inst Singapore, Singapore 138672, Singapore. Univ Calif San Diego, Dept Math, San Diego, CA 92093 USA. NHGRI, NISC, NIH, Bethesda, MD 20892 USA.;Pontius, JU, SAIC Frederick Inc, Lab Genom Divers, NCI Frederick, Frederick, MD 21702 USA.;Pontiusj@ncifcrf.gov Obrien@ncifcrf.gov
    1. Year: 2007
    2. Date: Nov
  1. Journal: Genome Research
    1. 17
    2. 11
    3. Pages: 1675-1689
  2. Type of Article: Article
  3. ISSN: 1088-9051
  1. 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 -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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External Sources

  1. DOI: 10.1101/gr.6380007
  2. PMID: 17975172
  3. PMCID: PMC2045150
  4. WOS: 000250641700014

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