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Mouse Models and the Genetics of Diabetes Is There Evidence for Genetic Overlap Between Type 1 and Type 2 Diabetes?

机译:小鼠模型和糖尿病遗传学是否有证据表明1型和2型糖尿病之间存在遗传重叠?

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In humans, both type 1 and type 2 diabetes exemplify genetically heterogeneous complex diseases in which epi-genetic factors contribute to underlying genetic susceptibility. Extended human pedigrees often show inheritance of both diabetes types. A common pathophysiological denominator in both disease forms is pancreatic β-cell exposure to proinflammatory cytokines. Hence, it is intuitive that systemically expressed genes regulating β-cell ability to withstand chronic diabetogenic stress may represent a component of shared susceptibility to both major disease forms. In this review, the authors assemble evidence from genetic experiments using animal models developing clearly distinct diabetes syndromes to inquire whether some degree of overlap in genes contributing susceptibility can be demonstrated. The conclusion is that although overlap exists in the pathophysiological insults leading to β-cell destruction in the currently studied rodent models, the genetic bases seem quite distinct.
机译:在人类中,1型和2型糖尿病都代表了遗传异质性复杂疾病,其中表观遗传因素导致潜在的遗传易感性。扩展的人谱系通常显示两种糖尿病的遗传。两种疾病形式中常见的病理生理指标是胰腺β细胞暴露于促炎细胞因子。因此,很直观的是,系统表达的调节β细胞抵抗慢性糖尿病的压力的基因可能代表了两种主要疾病共有的易感性。在这篇综述中,作者从遗传实验中收集的证据使用了发展出明显不同的糖尿病综合征的动物模型,以询问是否可以证明易感基因的某种程度的重叠。结论是,尽管在目前研究的啮齿动物模型中,导致β细胞破坏的病理生理损伤中存在重叠,但其遗传基础似乎相当不同。

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