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纸质出版:2012
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李武县,徐勇,李紫微,乔王敏,曾君,戴勇,涂植光.唐氏综合征胎儿脐带血单个核细胞microRNA差异表达研究[J].陆军军医大学学报(原第三军医大学学报),2012,34(19):1944-1948.
Li Wuxian,Xu Yong,Li Ziwei,Qiao Wangmin,Zeng Jun,Dai Yong,Tu Zhiguang.microRNA expression profiles of mononuclear cells from Down syndrome fetal cord blood[J].J Amry Med Univ (J Third Mil Med Univ),2012,34(19):1944-1948.
李武县,徐勇,李紫微,乔王敏,曾君,戴勇,涂植光.唐氏综合征胎儿脐带血单个核细胞microRNA差异表达研究[J].陆军军医大学学报(原第三军医大学学报),2012,34(19):1944-1948. DOI:
Li Wuxian,Xu Yong,Li Ziwei,Qiao Wangmin,Zeng Jun,Dai Yong,Tu Zhiguang.microRNA expression profiles of mononuclear cells from Down syndrome fetal cord blood[J].J Amry Med Univ (J Third Mil Med Univ),2012,34(19):1944-1948. DOI:
目的 检测唐氏综合征(Down syndrome,DS)胎儿和正常胎儿脐带血单个核细胞全基因组microRNA(miRNA)的差异表达。 方法 运用Solexa高通量测序技术对6 例DS胎儿(DS组)和6 例正常胎儿(对照组)脐带血单个核细胞miRNA表达水平进行检测,比较分析2组miRNA表达的差异,并用Stem-loop qRT-PCR对Solexa测序结果进行验证。 结果 2组样本显著性差异表达miRNA有167 种,8 种miRNA在DS组样本中表达上调,159 种miRNA表达下调;还有38 种和139 种miRNA分别特异性表达于DS组和对照组样本中;21号染色体上5个miRNA,除miR-802在DS组中高表达外,miR-99a、let-7c、miR-125b和miR-155均低表达。 结论 DS胎儿和健康胎儿脐带血单个核细胞miRNA的表达差异显著,可能与DS胎儿免疫系统的发育缺陷及DS胎儿循环T、B淋巴细胞数目的减少有关;差异显著和特异性表达的miRNA可作为DS胎儿潜在的产前筛查诊断指标。
Objective To detect the differentially expressed miRNAs in mononuclear cells from Down syndrome (DS) fetal cord blood. Methods Solexa high-throughput sequencing technology was conducted to evaluate the miRNA expression in 6 pairs of fetal cord blood mononuclear cells samples from DS fetuses (DS group) and normal fetuses (control group). Stem-loop qRT-PCR was performed to verify the results of Solexa sequencing. Results A total of 167 miRNAs were found significantly dysregulated expression in the DS fetal cord blood mononuclear cells compared to the controls. And there were 8 up-regulated miRNAs and 159 down-regulated miRNAs in DS group. Moreover
38 miRNAs and 139 miRNAs were specifically expressed in the DS group and control group
respectively. For the 5 miRNAs encoded by 21 chromosome
with the exception of miR-802
which was up-regulated in DS group
the other 4 Hsa21-derived miRNAs (i.e.
hsa-miR-99a
let-7c
miR-125b
and miR-155) displayed reduced expression. Conclusion These results suggested that there is a significant difference between the expression patterns of miRNAs in the DS group and control group
which may be related to the immune deficiency of DS fetus
and the decrease of T/B lymphocytes in DS fetal circulation. The significantly dysregulated and specifically expressed miRNAs are potential prenatal diagnosis biomarkers for DS fetus.
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