Weiss Heike, Arndt Tanja, Jörns Anne, Lenzen Sigurd, Cuppen Edwin, Hedrich Hans J, Tiedge Markus, Wedekind Dirk
Institute of Clinical Biochemistry, Hannover Medical School, 30623, Hannover, Germany,
Mamm Genome. 2008 Apr;19(4):292-7. doi: 10.1007/s00335-008-9102-4. Epub 2008 Mar 21.
The LEW.1AR1-iddm rat is an animal model of human type 1 diabetes mellitus (T1DM) with an autosomal recessive mode of inheritance. T1DM susceptibility loci could be localized on chromosome (RNO) 20 in the major histocompatibility complex region (Iddm1) and on RNO1 (Iddm8, Iddm9) in a BN backcross cohort. In this study the impact of the different susceptibility regions on diabetes development was investigated in a backcross population of the diabetes-resistant PAR strain. A cohort of 130 [(PAR x LEW.1AR1-iddm) x LEW.1AR1-iddm] N2 rats was monitored for blood glucose and analyzed by linkage analysis. Sixteen percent of the PAR backcross animals developed T1DM. Genetic analysis revealed significant linkage to T1DM in the MHC region on RNO20p12. In contrast to the linkage analysis of the BN backcross cohort, only one susceptibility locus for T1DM could be identified on RNO1. This susceptibility region on RNO1 mapped to the telomeric end corresponding to Iddm8. Eighty-nine percent of diabetic PAR backcross animals were homozygous for Iddm8. The Iddm9 diabetes susceptibility region showed no linkage to diabetes in the PAR backcross cohort. The data of this study provide evidence that the mutation leading to T1DM in the LEW.1AR1-iddm rat is located at the telomeric end of RNO1 corresponding to Iddm8.
LEW.1AR1-iddm大鼠是一种具有常染色体隐性遗传模式的人类1型糖尿病(T1DM)动物模型。在一个BN回交群体中,T1DM易感基因座可定位在主要组织相容性复合体区域的20号染色体(RNO)上(Iddm1),以及RNO1上(Iddm8、Iddm9)。在本研究中,在抗糖尿病PAR品系的回交群体中研究了不同易感区域对糖尿病发生发展的影响。对一组130只[(PAR×LEW.1AR1-iddm)×LEW.1AR1-iddm] N2大鼠监测血糖,并通过连锁分析进行分析。16%的PAR回交动物发生了T1DM。遗传分析显示与RNO20p12上的MHC区域的T1DM存在显著连锁。与BN回交群体的连锁分析不同,在RNO1上仅鉴定出一个T1DM易感基因座。RNO1上的这个易感区域定位于对应于Iddm8的端粒末端。89%的糖尿病PAR回交动物在Iddm8位点是纯合的。在PAR回交群体中,Iddm9糖尿病易感区域与糖尿病无连锁关系。本研究数据提供了证据,表明导致LEW.1AR1-iddm大鼠发生T1DM的突变位于RNO1对应于Iddm8的端粒末端。