Owerbach David, Piña Lazaro, Gabbay Kenneth H
Molecular Diabetes and Metabolism Section and the Harry B. and Aileen B. Gordon Diabetes Research Center, Department of Pediatrics, Baylor College of Medicine, Houston, Texas 77030, USA.
Diabetes. 2004 Jul;53(7):1890-3. doi: 10.2337/diabetes.53.7.1890.
The IDDM5 gene, which is identified by whole-genome searches, is located on chromosome 6q25. TAB2 (MAP3K7IP2 [mitogen-activating protein kinase kinase kinase 7 interacting protein 2]) is a potential candidate gene for type 1 diabetes because it is located on chromosome 6q25 and is involved in nuclear factor (NF)-kappaB regulation. We have conducted familial association studies using 478 families and demonstrate that a type 1 diabetes susceptibility gene resides within a 212-kb region containing the TAB2 gene (Tsp = 1.0 x 10(-2) to 4.0 x 10(-4)). No amino acid polymorphisms were detected in TAB2; however, multiple single nucleotide polymorphisms (SNPs) found within 5' untranslated, 3' untranslated, and intron regions were associated with type 1 diabetes susceptibility. Two additional genes, LOC340152, a predicted gene with currently unknown function, and SMT3, which has homology to SUMO (small ubiquitin-related modifier) were found within the 212-kb region and were associated with type 1 diabetes susceptibility. Functional studies of the three genes will be required to determine their biological relevance to type 1 diabetes. However, both TAB2 and SUMO are involved in NF-kappaB activation and may thus be involved in type 1 diabetes through apoptosis in pancreatic beta-cells.
通过全基因组搜索鉴定出的IDDM5基因位于6号染色体的6q25区域。TAB2(丝裂原活化蛋白激酶激酶激酶7相互作用蛋白2,即MAP3K7IP2)是1型糖尿病的一个潜在候选基因,因为它位于6号染色体的6q25区域,且参与核因子(NF)-κB的调控。我们利用478个家庭进行了家族关联研究,结果表明1型糖尿病易感性基因位于一个包含TAB2基因的212 kb区域内(Tsp = 1.0×10⁻²至4.0×10⁻⁴)。在TAB2中未检测到氨基酸多态性;然而,在5'非翻译区、3'非翻译区和内含子区域发现的多个单核苷酸多态性(SNP)与1型糖尿病易感性相关。在这个212 kb区域内还发现了另外两个基因,LOC340152(一个目前功能未知的预测基因)和与SUMO(小泛素相关修饰物)具有同源性的SMT3,它们也与1型糖尿病易感性相关。需要对这三个基因进行功能研究,以确定它们与1型糖尿病的生物学相关性。然而,TAB2和SUMO都参与NF-κB的激活,因此可能通过胰腺β细胞的凋亡参与1型糖尿病的发生。