Document Detail


Identification of genetic variation and putative regulatory regions in bovine CARD15.
MedLine Citation:
PMID:  16897345     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Mutations in caspase recruitment domain 15 (CARD15) are associated with susceptibility to Crohn's disease and Blau Syndrome. We performed comparative analyses of the bovine, murine, and human CARD15 transcripts to elucidate functionality of bovine CARD15 and examine its potential role in bovine disease resistance. Comparative analyses of intronic sequence across seven divergent species were performed to identify putative regulatory element binding motifs. High levels of interspecies conservation in sequence, genomic structure, and protein domains were detected indicating common functionality for CARD15 in cattle, human, and mouse. We identified species-specific regulatory elements in the 5' and 3' untranslated regions, suggesting that modes of regulation may have diverged across species. Thirty-one conserved putative regulatory element binding motifs were identified in the CARD15 intronic sequence of seven species. To assess the extent of genetic diversity within bovine CARD15, 41 individuals from two subspecies were sequenced and screened for polymorphisms. Thirty-six single nucleotide polymorphisms (SNPs) were identified. Finally, 20 subspecies-specific haplotypes were predicted with 7 and 13 unique haplotypes explaining the diversity within B. taurus taurus and B. taurus indicus animals, respectively. Strong evidence for a simple causal relationship between these SNP loci and their haplotypes with Johne's disease was not detected.
Authors:
Kristen H Taylor; Jeremy F Taylor; Stephen N White; James E Womack
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Publication Detail:
Type:  Comparative Study; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.     Date:  2006-08-04
Journal Detail:
Title:  Mammalian genome : official journal of the International Mammalian Genome Society     Volume:  17     ISSN:  0938-8990     ISO Abbreviation:  Mamm. Genome     Publication Date:  2006 Aug 
Date Detail:
Created Date:  2006-08-16     Completed Date:  2006-10-25     Revised Date:  2008-11-21    
Medline Journal Info:
Nlm Unique ID:  9100916     Medline TA:  Mamm Genome     Country:  United States    
Other Details:
Languages:  eng     Pagination:  892-901     Citation Subset:  IM    
Affiliation:
Department of Veterinary Pathobiology, Texas A&M University, College Station, Texas 77843-4467, USA.
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MeSH Terms
Descriptor/Qualifier:
3' Untranslated Regions / genetics
5' Untranslated Regions / genetics
Animals
Cattle / genetics*
Chromosome Mapping
Conserved Sequence
Genetic Variation*
Haplotypes
Humans
Intracellular Signaling Peptides and Proteins / genetics*
Mice
Nod2 Signaling Adaptor Protein
Polymorphism, Single Nucleotide
Regulatory Elements, Transcriptional / genetics*
Chemical
Reg. No./Substance:
0/3' Untranslated Regions; 0/5' Untranslated Regions; 0/Intracellular Signaling Peptides and Proteins; 0/NOD2 protein, human; 0/Nod2 Signaling Adaptor Protein

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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