首页> 外文OA文献 >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
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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

机译:β-细胞转录因子和糖尿病:在日本患者中编码基因的基因中没有糖尿病相关突变的证据表明日本患者的肌肤分化4(Neurod4)。

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摘要

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.
机译:基本螺旋环 - 螺旋(BHLH)转录因子家族在内分泌胰腺的正常发育和功能中起重要作用。编码该家庭的一个成员的基因中的杂合子突变Neurod1 /β2与单一的糖尿病的单一形式有关,其在许多方面类似于年轻(堪称)的成熟型糖尿病。该结果促使我们筛选编码相关的BHLH转录因子的基因,该因子也表达糖尿病相关突变。我们筛选了57个无关的日本受试者,临床诊断为神经元4 / Math-3 / Ath-3基因(Neurod4)中的突变突变。该分析揭示了七种常见的多态性,其与模型无关,包括在5' - 未转换区域(UTR)中的五(-477g / a,-436dela,-324delt,-107instttt,和-104t / c [cDNA序列])和3'-UTR(1027c / t和1076c / a)中的两个。在一个模拟的受试者和两个非糖尿病对象中,在杂合状态下发现畸形突变K68T(203A / c)。我们的研究结果表明Neurod4的遗传变异不是日语常见的常见原因。

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