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甲基化CpG 结合域蛋白 4 基因单核苷酸多态性与中国人群免疫性血小板减少性紫癜的易感性。

Single nucleotide polymorphism in the methyl-CpG binding domain 4 gene and the risk for immune thrombocytopenic purpura in Chinese population.

机构信息

State Key Laboratory of Experimental Hematology, Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Tianjin 300020, PR China.

出版信息

Platelets. 2010;21(2):132-6. doi: 10.3109/09537100903474365.

Abstract

Epigenetics might contribute to autoimmune diseases including immune thrombocytopenic purpura (ITP). Methyl-CpG binding domain protein 4 (MBD4) plays an important role in DNA methylation and transcriptional regulation of gene expression. The polymorphism of the MBD4 gene may influence MBD4 activity on gene expression profiles, thereby influencing individual susceptibility to ITP. To verify this hypothesis, we investigated the association between the MBD4 polymorphism and the risk for ITP in the Chinese population. The polymorphism of MBD4 rs140693 was genotyped by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP). In this study, there was no significant difference in genotype and alleles distribution between the ITP patients and the controls. Similar results were observed between the two groups when stratified by age and disease course including acute childhood, chronic childhood, acute adult and chronic adult. In the conclusion, MBD4 polymorphism may not be a stratification marker to predict the susceptibility to ITP, at least in Chinese population.

摘要

表观遗传学可能导致自身免疫性疾病,包括免疫性血小板减少性紫癜(ITP)。甲基化CpG 结合域蛋白 4(MBD4)在 DNA 甲基化和基因表达的转录调控中发挥重要作用。MBD4 基因的多态性可能会影响 MBD4 对基因表达谱的活性,从而影响个体对 ITP 的易感性。为了验证这一假设,我们研究了 MBD4 多态性与中国人群 ITP 风险之间的关系。通过聚合酶链反应-限制性片段长度多态性(PCR-RFLP)对 MBD4 rs140693 多态性进行了基因分型。在这项研究中,ITP 患者与对照组之间在基因型和等位基因分布上没有显著差异。在按年龄和疾病病程(包括儿童急性、儿童慢性、成人急性和成人慢性)分层时,两组之间也观察到了类似的结果。综上所述,MBD4 多态性可能不是预测 ITP 易感性的分层标志物,至少在中国人群中不是。

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