Article
Genetic dissection reveals diabetes loci proximal to the gimap5 lymphopenia gene.
Department of Clinical Sciences, Lund University, Clinical Research Center, Malmö, Sweden.
Physiological Genomics (impact factor:
2.73).
04/2009;
38(1):89-97.
DOI:10.1152/physiolgenomics.00015.2009
pp.89-97
Source: PubMed
- Citations (2)
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Cited In (0)
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Article: Refinement of the Iddm4 diabetes susceptibility locus reveals TCRVbeta4 as a candidate gene.
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ABSTRACT: Iddm4 is a dominant non-major histocompatibility complex (MHC) determinant of diabetes susceptibility in BBDR rats treated with poly I:C, plus depletion of regulatory T cells. In congenic MHC-identical normal WF rats, Iddm4(d) sensitively and specifically predicts induced diabetes. We report a new diabetes-susceptible subcongenic line that carries Iddm4 in a < 2.6 megabase interval. Candidate genes include the T cell receptor beta chain variable (TCRVbeta) family. We found that TCRVbeta4 in WF rats contains a stop codon, whereas 5/5 diabetes-susceptible rat strains express TCRVbeta4. We conclude that Iddm4-mediated diabetes resistance in rats may be due to a recessive protective mutation in TCRVbeta4.Annals of the New York Academy of Sciences 05/2007; 1103:128-31. · 3.15 Impact Factor -
Article: Diabetes segregates as a single locus in crosses between inbred BB rats prone or resistant to diabetes.
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ABSTRACT: Diabetes-prone (DP) BB rats spontaneously develop insulin-dependent diabetes resembling type 1 diabetes mellitus in man. They also exhibit lifelong T cell deficiency. The segregation of both diabetes and lymphopenia was studied in crosses between this inbred line of rats and the related but nondiabetic and nonlymphopenic inbred diabetes-resistant (DR) BB rat line. Diabetes segregated as a single, autosomal recessive trait and was always accompanied by lymphopenia. Among the limited number of differences in the genomic DNA sequences of the two lines, DP and DR BB, one may account for the development of diabetes and lymphopenia in the DP BB rats. It may be possible to screen the genomic DNA for such differences to detect a marker for the phenotypes.Journal of Experimental Medicine 08/1991; 174(1):297-300. · 13.85 Impact Factor
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Keywords
2 Mb interval
47% protection
candidate genes
Coding sequence analysis
complete T1D protection
congenic DRF.(f/f)
congenic sublines
DR.(lyp/lyp)). Comparative analysis
F344 DNA introgressed proximal
genetic factor(s)
genotyped
gimap5 lymphopenia gene
inbred BBDR
low-grade pancreatic mononuclear cell infiltration
nondiabetic rats
positional candidate genes
RNO4 region 1 interval
spontaneous T1D
two genetic loci 7 Mb
type 1 diabetes