Three loci on mouse chromosome 6 influence onset and final incidence of type 1 diabetes in NOD.C3H congenic strains

被引:60
作者
Rogner, UC
Boitard, C
Morin, J
Melanitou, E
Avner, P
机构
[1] Inst Pasteur, CNRS URS 1947, F-75724 Paris 15, France
[2] Hop Cochin St Vincent de Paul, ICGM, INSERM U342, F-75014 Paris, France
关键词
D O I
10.1006/geno.2001.6508
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The development of insulin-dependent diabetes mellitus in both human and mouse is dependent on the interaction between genetic and environmental factors. The analysis of newly created NOD.C3H congenic strains for spontaneous and cyclophosphamide-induced diabetes has allowed the definition of three controlling genetic loci on mouse chromosome 6. A NOD-derived susceptibility allele at the Idd6 locus strongly influences the onset of diabetes in spontaneous diabetes. A NOD-derived resistance allele at the Idd19 locus affects the final diabetes incidence observed in both models, while a novel locus, provisionally termed Idd20, appears to control Idd19 in an epistatic manner, Decreased diabetes incidence is observed in CY-induced diabetes when Idd20 is homozygous for the C3H allele, while heterozygosity is associated with an increase in diabetes incidence. The Idd20 Idd19, and Idd6 candidate regions fall respectively within genetically defined intervals of 4, 7, and 4.5 cM on mouse chromosome 6, From our YAC contig, Idd6 would appear to localize within a ca. 1.5-Mb region on distal chromosome 6. (C) 2001 Academic Press.
引用
收藏
页码:163 / 171
页数:9
相关论文
共 62 条
[1]   Acceleration of autoimmune diabetes by cyclophosphamide is associated with an enhanced IFN-γ secretion pathway [J].
Ablamunits, V ;
Quintana, F ;
Reshef, T ;
Elias, D ;
Cohen, IR .
JOURNAL OF AUTOIMMUNITY, 1999, 13 (04) :383-392
[2]   CD27, a member of the tumor necrosis factor receptor superfamily, activates NF-KB and stress-activated protein kinase/c-Jun N-terminal kinase via TRAF2, TRAF5, and NF-KB-inducing kinase [J].
Akiba, H ;
Nakano, H ;
Nishinaka, S ;
Shindo, M ;
Kobata, T ;
Atsuta, M ;
Morimoto, C ;
Ware, CF ;
Malinin, NL ;
Wallach, D ;
Yagita, H ;
Okumura, K .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (21) :13353-13358
[3]   Checkpoints in the progression of autoimmune disease: Lessons from diabetes models [J].
Andre, I ;
Gonzalez, A ;
Wang, B ;
Katz, J ;
Benoist, C ;
Mathis, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (06) :2260-2263
[4]   A POLYMORPHIC LOCUS NEAR THE HUMAN INSULIN GENE IS ASSOCIATED WITH INSULIN-DEPENDENT DIABETES-MELLITUS [J].
BELL, GI ;
HORITA, S ;
KARAM, JH .
DIABETES, 1984, 33 (02) :176-183
[5]   SUSCEPTIBILITY TO HUMAN TYPE-1 DIABETES AT IDDM2 IS DETERMINED BY TANDEM REPEAT VARIATION AT THE INSULIN GENE MINISATELLITE LOCUS [J].
BENNETT, ST ;
LUCASSEN, AM ;
GOUGH, SCL ;
POWELL, EE ;
UNDLIEN, DE ;
PRITCHARD, LE ;
MERRIMAN, ME ;
KAWAGUCHI, Y ;
DRONSFIELD, MJ ;
POCIOT, F ;
NERUP, J ;
BOUZEKRI, N ;
CAMBONTHOMSEN, A ;
RONNINGEN, KS ;
BARNETT, AH ;
BAIN, SC ;
TODD, JA .
NATURE GENETICS, 1995, 9 (03) :284-292
[6]   Biochemical characterization of a beta cell membrane fraction antigenic for autoreactive T cell clones [J].
Bergman, B ;
McManaman, JL ;
Haskins, K .
JOURNAL OF AUTOIMMUNITY, 2000, 14 (04) :343-351
[7]  
BONHOMME JF, 1989, GENETIC VARIANTS STR, P642
[8]   DEATH OF A BETA-CELL - HOMICIDE OR SUICIDE [J].
BOTTAZZO, GF .
DIABETIC MEDICINE, 1986, 3 (02) :119-130
[9]   TYPE-I DIABETES - A CHRONIC AUTOIMMUNE-DISEASE OF HUMAN, MOUSE, AND RAT [J].
CASTANO, L ;
EISENBARTH, GS .
ANNUAL REVIEW OF IMMUNOLOGY, 1990, 8 :647-679
[10]   MUTATIONS IN MICE THAT INFLUENCE NATURAL-KILLER (NK) CELL-ACTIVITY [J].
CLARK, EA ;
SHULTZ, LD ;
POLLACK, SB .
IMMUNOGENETICS, 1981, 12 (5-6) :601-613