Makino S, Muraoka Y, Kishimoto Y, Hayashi Y
Jikken Dobutsu. 1985 Oct;34(4):425-31. doi: 10.1538/expanim1978.34.4_425.
Non-obese diabetic (NOD) mice spontaneously develop diabetic signs akin to those of Type I diabetes in man. Insulitis, i.e., lymphocytic infiltration around and into the pancreatic islets is one of the characteristics of such mice. It is also the etiologic pathological lesion in the development of diabetes mellitus in NOD mice. Thus, we chose insulitis as a marker for genetic analysis of the development of diabetes mellitus in NOD mice and clarified the mode of its inheritance. In breeding studies between NOD and C57BL/6J mice, insulitis was not observed in the F1 and (F1 X C57BL/6J) backcross generations, but was found with incidences of 3.9% in females and 1.4% in males in the F2 generation and 23.7% in females and 12.1% in males in the (F1 X NOD) backcross generation. These incidences in the F2 and (F1 X NOD) backcross females corresponded approximately to 1/16 and 1/4 of the incidences of 89.7% in the NOD females, respectively. A similar relationship was observed between the F2 and (F1 X NOD) backcross males and the NOD males. When the gene expressivity of both sexes for a double recessive homozygote was assumed to be the incidences of insulitis in 9-week-old NOD females and males, respectively, the expected numbers of both sexes with and without insulitis in the F2 and backcross generations agreed well with the observed ones. These observations suggest that two recessive genes on independent autosomal chromosomes are necessary for the development of insulitis in NOD mice.
非肥胖糖尿病(NOD)小鼠会自发出现类似于人类I型糖尿病的糖尿病症状。胰岛炎,即围绕胰岛并侵入胰岛的淋巴细胞浸润,是这类小鼠的特征之一。它也是NOD小鼠糖尿病发展过程中的病因病理病变。因此,我们选择胰岛炎作为NOD小鼠糖尿病发展遗传分析的标志物,并阐明了其遗传模式。在NOD和C57BL/6J小鼠的杂交研究中,F1代和(F1×C57BL/6J)回交代未观察到胰岛炎,但在F2代中,雌性发病率为3.9%,雄性发病率为1.4%;在(F1×NOD)回交代中,雌性发病率为23.7%,雄性发病率为12.1%。F2代和(F1×NOD)回交代雌性的这些发病率分别约为NOD雌性发病率89.7%的1/16和1/4。在F2代和(F1×NOD)回交代雄性与NOD雄性之间也观察到类似关系。假设双隐性纯合子两性的基因表达率分别为9周龄NOD雌性和雄性的胰岛炎发病率,则F2代和回交代中有胰岛炎和无胰岛炎的两性预期数量与观察值吻合良好。这些观察结果表明,NOD小鼠发生胰岛炎需要两条独立常染色体上的两个隐性基因。