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PD-1 gene haplotype is associated with the development of type 1 diabetes mellitus in Japanese children

机译:PD-1基因单倍型与日本儿童1型糖尿病的发生有关

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摘要

Interaction between Programmed cell death-1 (PD-1), a member of costimulatory molecules, and its receptors Programmed cell Death-1 Ligand 1 (PD-L1) and Programmed cell Death-1 Ligand 2 (PD-L2), play an important role in the negative regulation of immune reactions. It was shown that a polymorphism in a regulatory site of the PD-1 gene was associated with susceptibility to several autoimmune diseases in various ethnic groups, whereas the contribution of the PD-1 gene or its ligand genes to the onset of type 1 diabetes (T1D) mellitus in the Japanese population remains unknown. We first screened PD-1, PD-L1, and PD-L2 genes for polymorphisms in the Japanese population, and then investigated the frequencies of polymorphisms in patients with T1D mellitus in comparison with healthy controls. In total, we identified 26 polymorphic sites within these genes, and then 23 polymorphisms with minor allele frequencies greater than 5% were intensively analyzed for genotyping in the patients and the controls. As a result, allele and genotype frequencies of the polymorphism numbers 2, 3, 4, 5, 6, and 8 in the PD-1 gene were different to some extent between the patients and the controls with P < 0.05, which did not reach statistical significance after the correction of multiple comparisons. Allele or genotype frequencies of any SNPs in the PD-L1 or PD-L2 gene did not show differences between the patients and the controls. The frequencies of the estimated haplotypes, those of which consisted of polymorphism numbers 2, 3, 4, 5, 6, and 8 in the PD-1, were significantly different between the patients and the controls (P = 0.00095). The in vitro assessment for a transcription activity of each haplotype of the PD-1 gene by luciferase assay did not demonstrate a functional difference between the haplotypes. In conclusion, the genetic evaluation by association study demonstrated that the PD-1 gene was a predisposing gene to the development of T1D mellitus in the Japanese population.
机译:共刺激分子成员程序化细胞死亡1(PD-1)和其受体程序化细胞死亡1配体1(PD-L1)和程序性细胞死亡1配体2(PD-L2)之间的相互作用在免疫反应的负调节中起重要作用。结果表明,PD-1基因调控位点的多态性与不同种族对几种自身免疫性疾病的易感性有关,而PD-1基因或其配体基因对1型糖尿病的发作有一定的影响(日本人口中的T1D)癌症仍然未知。我们首先筛选了PD-1,PD-L1和PD-L2基因在日本人群中的多态性,然后与健康对照组相比,研究了T1D患者的多态性频率。总的来说,我们在这些基因中鉴定出26个多态性位点,然后对23个具有等位基因频率大于5%的多态性进行了深入分析,以分析患者和对照组的基因型。结果,PD-1基因中多态性数2、3、4、5、6和8的等位基因和基因型频率在患者和对照组之间有一定程度的差异,P <0.05,未达到校正多个比较后具有统计学意义。 PD-L1或PD-L2基因中任何SNP的等位基因或基因型频率在患者和对照组之间均未显示差异。估计的单体型的频率在PD-1中由2、3、4、5、6和8的多态性组成,在患者和对照组之间存在显着差异(P = 0.00095)。通过荧光素酶测定法对PD-1基因的每个单倍型的转录活性进行的体外评估未显示出单倍型之间的功能差异。总之,通过关联研究进行的遗传评估表明,PD-1基因是日本人群T1D发病的易感基因。

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  • 来源
    《Human Genetics》 |2007年第2期|223-232|共10页
  • 作者单位

    Department of Pediatrics Graduate School of Medical Sciences Kyushu University Maidashi 3-1-1 Higashiku Fukuoka 812-8582 Japan;

    Department of Pediatrics Graduate School of Medical Sciences Kyushu University Maidashi 3-1-1 Higashiku Fukuoka 812-8582 Japan;

    Department of Pediatrics Graduate School of Medical Sciences Kyushu University Maidashi 3-1-1 Higashiku Fukuoka 812-8582 Japan;

    Department of Pediatrics Graduate School of Medical Sciences Kyushu University Maidashi 3-1-1 Higashiku Fukuoka 812-8582 Japan;

    Department of Pediatrics Graduate School of Medical Sciences Kyushu University Maidashi 3-1-1 Higashiku Fukuoka 812-8582 Japan;

    Department of Endocrinology and Metabolism Fukuoka Children’s Hospital Fukuoka Japan;

    Department of Pediatrics Graduate School of Medical Sciences Kyushu University Maidashi 3-1-1 Higashiku Fukuoka 812-8582 Japan;

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