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Capn10,一种在OLETF大鼠中导致2型糖尿病的候选基因。

Capn10, a candidate gene responsible for type 2 diabetes mellitus in the OLETF rat.

作者信息

Muramatsu Youji, Taniguchi Yukio, Kose Hiroyuki, Matsumoto Kozo, Yamada Takahisa, Sasaki Yoshiyuki

机构信息

Department of Food Sciences, Shizuoka Eiwa Gakuin University Junior College, Ikeda, Shizuoka, Shizuoka 422-8005, Japan.

出版信息

IUBMB Life. 2003 Sep;55(9):533-7. doi: 10.1080/15216540310001620977.

Abstract

The rat strain Otsuka Long-Evans Tokushima Fatty (OLETF) is an animal model for type 2 diabetes mellitus. Nidd8/of has been identified as one of 14 quantitative trait loci (QTLs) involved in the diabetes by a whole genome search in 160 F2 progenies obtained by mating the OLETF and F344 rats. Comparative mapping between human and rat indicated that the Nidd8/of genomic region, near D9rat21 on rat chromosome 9, contains the calpain10 (Capn10) gene, which is putative type 2 diabetes-susceptibility gene in humans. In this study, we found no difference in Capn10 mRNA expression in the heart, liver, skeletal muscle and pancreas between OLETF and F344 rats at 5 and 10 weeks of age. However, we found a single nucleotide polymorphism (SNP) (A/A genotype in OLETF and G/G genotype in F344 and LETO rats) at the base 583 downstream from the translation start site in the rat Capn10 cDNA sequence. This SNP was deduced to substitute serine (OLETF) for glycine (F344 and LETO) at the 195 amino acid residue within the protease domain of rat Capn10. Because serine is generally not interchangeable with glycine in respect of the protein structure and function, it was deduced that the A/A genotype in OLETF is not a 'safe' mutation. This non-conservative amino acid substitution might be associated with susceptibility to type 2 diabetes in OLETF rats.

摘要

大冢长-伊文斯德岛肥胖大鼠(OLETF)品系是2型糖尿病的动物模型。通过对OLETF大鼠与F344大鼠杂交获得的160只F2后代进行全基因组搜索,已确定Nidd8/of是与糖尿病相关的14个数量性状基因座(QTL)之一。人与大鼠之间的比较定位表明,大鼠9号染色体上靠近D9rat21的Nidd8/of基因组区域包含钙蛋白酶10(Capn10)基因,该基因被认为是人类2型糖尿病的易感基因。在本研究中,我们发现5周龄和10周龄时,OLETF大鼠与F344大鼠在心脏、肝脏、骨骼肌和胰腺中的Capn10 mRNA表达没有差异。然而,我们在大鼠Capn10 cDNA序列翻译起始位点下游583个碱基处发现了一个单核苷酸多态性(SNP)(OLETF大鼠为A/A基因型,F344大鼠和LETO大鼠为G/G基因型)。该SNP推断在大鼠Capn10蛋白酶结构域内的第195个氨基酸残基处,将丝氨酸(OLETF大鼠)替换为甘氨酸(F344大鼠和LETO大鼠)。由于就蛋白质结构和功能而言,丝氨酸通常不能与甘氨酸互换,因此推断OLETF大鼠中的A/A基因型不是一个“安全”的突变。这种非保守氨基酸取代可能与OLETF大鼠对2型糖尿病的易感性有关。

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