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β细胞转录因子与糖尿病:在日本成年发病型糖尿病(MODY)患者中,未发现编码碱性螺旋-环-螺旋转录因子神经源性分化因子4(NEUROD4)的基因存在与糖尿病相关的突变。

beta-cell transcription factors and diabetes: no evidence for diabetes-associated mutations in the gene encoding the basic helix-loop-helix transcription factor neurogenic differentiation 4 (NEUROD4) in Japanese patients with MODY.

作者信息

Horikawa Y, Horikawa Y, Cox N J, Iwasaki N, Ogata M, Iwamoto Y, Schwitzgebel V, German M S, Bell G I

机构信息

Department of Biochemistry and Molecular Biology, The University of Chicago, Illinois, USA.

出版信息

Diabetes. 2000 Nov;49(11):1955-7. doi: 10.2337/diabetes.49.11.1955.

Abstract

The basic helix-loop-helix (bHLH) family of transcription factors plays an important role in the normal development and function of the endocrine pancreas. Heterozygous mutations in the gene encoding one member of this family, NeuroD1/BETA2, are associated with a monogenic form of diabetes that resembles maturity-onset diabetes of the young (MODY) in many respects. This result prompted us to screen the genes encoding related bHLH transcription factors that are also expressed in pancreatic islets for diabetes-associated mutations. We have screened 57 unrelated Japanese subjects with a clinical diagnosis of MODY for mutations in the NeuroD4/Math-3/ATH-3 gene (NEUROD4). This analysis revealed seven frequent polymorphisms that were not associated with MODY, including five in the 5'-untranslated region (UTR) (-477G/A, -436delA, -324delT, -107insTTTT, and -104T/C [cDNA sequences]) and two in the 3'-UTR (1027C/T and 1076C/A). A missense mutation, K68T (203A/C), was found in a heterozygous state in one MODY subject and two nondiabetic subjects. The results of our study suggest that genetic variation in NEUROD4 is not a common cause of MODY in Japanese.

摘要

转录因子的基本螺旋-环-螺旋(bHLH)家族在内分泌胰腺的正常发育和功能中起着重要作用。该家族的一个成员NeuroD1/BETA2编码基因的杂合突变与一种单基因形式的糖尿病相关,这种糖尿病在许多方面类似于青年发病的成年型糖尿病(MODY)。这一结果促使我们筛选在胰岛中也表达的相关bHLH转录因子编码基因,以寻找与糖尿病相关的突变。我们对57名临床诊断为MODY的不相关日本受试者进行了NeuroD4/Math-3/ATH-3基因(NEUROD4)突变筛查。该分析揭示了7种与MODY无关的常见多态性,包括5种位于5'-非翻译区(UTR)(-477G/A、-436delA、-324delT、-107insTTTT和-104T/C [cDNA序列])以及2种位于3'-UTR(1027C/T和1076C/A)。在一名MODY受试者和两名非糖尿病受试者中发现了杂合状态的错义突变K68T(203A/C)。我们的研究结果表明,NEUROD4的基因变异不是日本人群中MODY的常见病因。

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