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足月儿与早产儿脐血有核红细胞基因组DNA甲基化差异分析

Analysis of Genome-Wide DNA Methylation Differences in Umbilical Cord Blood Nucleated Red Blood Cells Between Term and Preterm Infants
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摘要 目的:采用甲基化基因芯片技术从全基因组水平分析足月儿与早产儿脐血有核红细胞DAN甲基化差异,筛选出可能与γ珠蛋白基因(HBG)表达相关的差异甲基化基因及生物信号通路。方法:收集足月产儿及早产儿各8例,取其脐血标本,分离脐血有核红细胞并提取基因组DNA,并对其进行亚硫酸氢盐转化。利用Illumina 850K甲基化芯片检测2组样本的DNA甲基化位点。筛选差异甲基化位点,并通过GO和KEGG富集分析得到差异甲基化基因的功能。结果:相较于早产组,足月组共筛选到4749个差异甲基化位点,其中低甲基化位点4359个,高甲基化位点390个。GO和KEGG分析结果显示,差异甲基化基因的功能主要涉及造血系统、生长发育过程、Wnt和Notch信号通路等。结论:本研究获得了足月组和早产组脐血有核红细胞在全基因组水平的差异甲基化位点,筛选出可能与γ→β珠蛋白基因表达转换相关的通路和基因。这为后续进一步研究HBG基因的表达调控机制提供了新的研究靶点。 Objective:To analyze the genome-wide DNA methylation differences in umbilical cord blood nucleated red blood cells(NRBCs)between term and preterm infants by using the methylation gene chip technology,and to screen the genes of differential methylation and biological signaling pathways which may be related to the expression ofγ-globin gene(HBG).Methods:Umbilical cord bloods of eight term infants and eight preterm infants were collected,and NRBCs of each sample was isolated,then genome DNA was extracted and bisulfite conversion was performed.The DNA methylation sites were detected by using the Illumina 850K BeadChip.Differential DNA methylation sites were screened,and the function of genes with differential methylation was analyzed by using GO and KEGG enrichment analysis.Results:Compared with the preterm group,4749 differential DNA methylation sites of term group were screened out,including 4359 hypomethylation sites and 390 hypermethylation sites.GO and KEGG analysis indicated that the function of genes with differential methylation mainly involved in the hemopoietic system,growth and development process,Wnt and Notch signal pathways.Conclusion:The differentical methylation sites at genome-wide level in umbilicar cord blood NRBC of term and preterm infants have been obtained,and the signal pathway and genes which possibily related with swiching the expression ofγ-globin gene toβ-globin gene have been screened-out.This study provide the new targets for studing the mechamism regulating expression of HBG gene.
作者 杨楠楠 罗振元 周曼 林虹 王薇 黄盛文 YANG Nan-Nan;LUO Zhen-Yuan;ZHOU Man;LIN Hong;WANG Wei;HUANG Sheng-Wen(Department of Laboratorial Medicine,Guizhou Provincial People′s Hospital,Guiyang 550002,Guizhou Province,China;Department of Obstetrics,Guizhou Provincial People′s Hospital,Guiyang 550002,Guizhou Province,China;Department of Obstetrics,Guiyang Maternal and Child Health Hospital,Guiyang 550003,Guizhou Province,China;Department of Obstetrics,The Second People′s Hospital of Guiyang,Guiyang 550023,Guizhou Province,China)
出处 《中国实验血液学杂志》 CAS CSCD 北大核心 2020年第3期942-947,共6页 Journal of Experimental Hematology
基金 国家自然科学基金(81660023) 贵州省科技合作计划项目(黔科合LH字[2015]7134号) 贵州省留学人员科技创新项目([2016]15号) 贵阳市科技创新平台计划(筑科合同[20161001]35号)。
关键词 甲基化芯片 γ珠蛋白基因 甲基化位点 脐血 有核红细胞 methylation gene chip γ-globin methylation sites umbilical cord blood nucleated red blood cells
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  • 1黄为民,钱新华,赵丹华,阳勇.黄芪多糖对K562细胞胎儿血红蛋白合成和细胞增殖的影响[J].实用儿科临床杂志,2009,24(9):687-688. 被引量:8
  • 2王文杰,白金叶,朱秀媛.血浆甘磷酰芥及代谢物的测定方法和大鼠口服药代动力学[J].药学学报,1993,28(10):738-743. 被引量:5
  • 3廖灿,徐湘民,黄以宁,李坚,钟燕芳,邱洛琳.反向点杂交法用于产前诊断β-地中海贫血60例分析[J].中华妇产科杂志,1996,31(6):348-350. 被引量:11
  • 4Suthat F,Premee W,Raewadee WJ,et al. Prental and post- nastal diagnoses of thalassemias and hemoglobinoipathies by HPLC [J]. Clinical chemistry,1998,4 (44) :740.
  • 5Tongsong T, Wanapirak C, Sirivatanapa P, et al. Prenatal control of severe thalassaemia: Chiang Mai Strategy [ J ]. P renat Diagn,2000,20(3 ) :229.
  • 6Keren DF,Hedstrom D, Gulbranson R, et al. Comparison of Sebia Capillarys capillary eleetrophoresis with the Pfimus high - pressure liquid chromatography in the evaluation of hemoglobinop- athies[J]. Am J Clin Pathol,2008,130(5) :824.
  • 7Cai SP, Wall J,Kan YW, et al. Reverse dot blot probes for screening of β- thalassemia Mutationsin Asians and American blacks[J]. Hum Mut,1994,3( 1 ) :59.
  • 8Walters MC. Gene therapy and bone marrow transplantation for thalassemia:changing of the guard[J].{H}Molecular Therapy,2010,(9):1577.
  • 9Thein SL,Menzel S,Lathrop M. Control of fetal hemoglobin:new insights emerging from genomics and clinical implications (R2):R216-R223.Hum Mol Genet[J].Hum Mol Genet,2009,(R2):R216-R223.
  • 10Pace BS,Zein S. Understanding mechanisms of garma-globin gene regulation to develop strategies for pharmacological fetal hemoglobin induction[J].{H}Development Dynamics,2006,(7):1727-1737.

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