Literature DB >> 9922397

Genotypic and phenotypic characterization of six new recombinant congenic strains derived from NOD/Shi and CBA/J genomes.

P C Reifsnyder1, J C Flynn, A L Gavin, E A Simone, J J Sharp, L Herberg, E H Leiter.   

Abstract

Recombinant Congenic Strains (RCS) are useful for dissecting complex polygenic traits. Here, we describe genetic and phenotypic characterization of six new RCS generated from outcrosses between NOD/Shi and CBA/LsLt, followed by sib mating of first backcross progeny (to CBA) for 20 generations, whereupon genetic and phenotypic analysis commenced. Four of the RCS were selected on the basis of residual heterozygosity present at F20 in one of the three original RCS. Contrary to expectations for RCS developed at first backcross, all derived at least 50% of the polymorphic markers typed from the NOD parental strain. Development of autoimmune insulin-dependent diabetes mellitus (IDDM) in NOD is a strain-specific characteristic. The major genetic component predisposing NOD mice to IDDM, their H2(g7) haplotype, was present in all RCS. Nevertheless, the presence of variable amounts of CBA genome at non-MHC loci conferred complete resistance in all RCS to spontaneous IDDM development, and rendered them strongly resistant to cyclophosphamide-induced IDDM. Although the RCS more resemble NOD in regard to certain strain-specific characteristics, such as prolificacy, an immunologic phenotype that was significantly reduced when compared to both parental strains was the number of peripheral CD8(+) T cells. Given the genetic characterization presented, these new RCS should prove valuable to investigators interested in studying genes controlling differential susceptibilities distinguishing the NOD and CBA inbred strain backgrounds.

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Year:  1999        PMID: 9922397     DOI: 10.1007/s003359900962

Source DB:  PubMed          Journal:  Mamm Genome        ISSN: 0938-8990            Impact factor:   2.957


  4 in total

1.  Sequence variation in promoter of Ica1 gene, which encodes protein implicated in type 1 diabetes, causes transcription factor autoimmune regulator (AIRE) to increase its binding and down-regulate expression.

Authors:  Samantha M Bonner; Susan L Pietropaolo; Yong Fan; Yigang Chang; Praveen Sethupathy; Michael P Morran; Megan Beems; Nick Giannoukakis; Giuliana Trucco; Michael O Palumbo; Michele Solimena; Alberto Pugliese; Constantin Polychronakos; Massimo Trucco; Massimo Pietropaolo
Journal:  J Biol Chem       Date:  2012-03-24       Impact factor: 5.157

2.  Two genetic loci regulate T cell-dependent islet inflammation and drive autoimmune diabetes pathogenesis.

Authors:  C J Fox; A D Paterson; S M Mortin-Toth; J S Danska
Journal:  Am J Hum Genet       Date:  2000-06-09       Impact factor: 11.025

3.  "Agouti NOD": identification of a CBA-derived Idd locus on Chromosome 7 and its use for chimera production with NOD embryonic stem cells.

Authors:  Jing Chen; Peter C Reifsnyder; Felix Scheuplein; William H Schott; Maria Mileikovsky; Sharon Soodeen-Karamath; Andras Nagy; Michael H Dosch; James Ellis; Friedrich Koch-Nolte; Edward H Leiter
Journal:  Mamm Genome       Date:  2005-10-29       Impact factor: 2.957

4.  Infection-dependent phenotypes in MHC-congenic mice are not due to MHC: can we trust congenic animals?

Authors:  Erin E McClelland; Kristy Damjanovich; Kyle Gardner; Zack J Groesbeck; Maggie S Ma; Megan Nibley; Kelly S Richardson; Maureen Wilkinson; Linda C Morrison; Paul Bernhardt; Wayne K Potts
Journal:  BMC Immunol       Date:  2004-07-09       Impact factor: 3.615

  4 in total

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