胰岛素
内科学
内分泌学
医学
胰岛素受体
错义突变
糖尿病
高胰岛素血症
胰岛素原
突变
外显子
自磷酸化
胰岛素抵抗
生物
生物化学
激酶
基因
蛋白激酶A
作者
Masato Kasuga,Mitsumasa Kishimoto,Mitsuru Hashiramoto,K Yonezawa,T Kazumi,Haruhiko Hagino,Kozui Shii
出处
期刊:PubMed
[National Institutes of Health]
日期:1992-09-01
卷期号:93 (9): 968-71
被引量:3
摘要
A novel mutation Arg1131-->Gln in the catalytic loop of insulin receptor (IR) associated with insulin resistant diabetes was detected. A 56-year-old male with hyperinsulinemia (fasting IRI 92 microU/ml) showed moderate impairment in glucose tolerance (HbAlc 7.0%, fructosamine 258 mumol/l, fasting glucose 119 mg/dl, maximum value of blood glucose during 75 g OGTT 220 mg/dl). While insulin binding to erythrocytes IR was normal, the insulin-induced autophosphorylation of the patient's erythrocytes IR in vivo showed marked decrease, suggesting this patient had some defect in the kinase domain (exon 17-21) of IR. PCR-SSCP analysis of kinase domain with a genomic DNA obtained from the patient's leucocytes indicated the presence of some mutations in exon 19. Sequencing analysis in M13 revealed a heterozygous mutation at a position 1131 (CGG-->CAG) substituting Gln for Arg. Four people of patient's family analyzed are revealed to have an identical missense mutation at the same position with the patient.
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