Institut de Biologie F Jacob, DRF/CEA, 92265, Fontenay aux Roses, France.
Computational and Systems Medicine, Department of Surgery and Cancer, Faculty of Medicine, Imperial College London, SW7 2AZ, London, UK; McGill University and Genome Quebec Innovation Centre, 740 Doctor Penfield Avenue, Montreal, QC, H3A 0G1, Canada.
Biochimie. 2017 Dec;143:56-65. doi: 10.1016/j.biochi.2017.08.012. Epub 2017 Aug 24.
The inbred Goto-Kakizaki (GK) rat strain is a unique model of spontaneous type 2 diabetes mellitus caused by naturally occurring genetic variants that have been selectively isolated from an outbred colony of Wistar rats. Genetic and genomic studies in experimental crosses and congenic strains of the GK have shed light on the complex etiopathogenesis of diabetes phenotypes in this model. Diabetes-related phenotypes in the GK are under polygenic control and distinct genetic loci regulate glucose tolerance, insulin secretion, β-cell mass and plasma lipids. Metabolome and transcriptome profiling data in GK crosses and congenics, combined with GK genome resequencing, have resulted in a comprehensive landscape of genomic regulations of metabolism that can disentangle causal relationships between GK variants and diabetes phenotypes. Application of systems biology and systems genetics in the GK has contributed to improve our understanding of the fundamental mechanisms regulating metabolism. The wealth of physiological, genetic and genomic information in this strain makes it one of the most powerful model systems to improve our understanding of genetic regulations of metabolism and for testing therapeutic solutions for diabetes.
近交系 Goto-Kakizaki(GK)大鼠是一种自发性 2 型糖尿病的独特模型,由自然发生的遗传变异引起,这些变异已从 Wistar 大鼠的杂交群体中被选择性分离出来。在 GK 的实验杂交和同源系中进行的遗传和基因组研究揭示了该模型中糖尿病表型的复杂病因发病机制。GK 中的糖尿病相关表型受多基因控制,不同的遗传位点调节葡萄糖耐量、胰岛素分泌、β细胞质量和血浆脂质。GK 杂交和同源系中的代谢组和转录组分析数据,加上 GK 基因组重测序,产生了代谢的全面基因组调控图谱,可以理清 GK 变异与糖尿病表型之间的因果关系。系统生物学和系统遗传学在 GK 中的应用有助于提高我们对调节代谢的基本机制的理解。该品系拥有丰富的生理、遗传和基因组信息,使其成为最强大的模型系统之一,可用于提高我们对代谢遗传调控的理解,并为糖尿病的治疗方法提供测试。