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DNA Methylation Changes at Promoters of Endothelial Cell-Enriched Genes during in vitro Differentiation.

机译:体外分化过程中内皮细胞富集基因启动子的DNA甲基化变化。

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摘要

This study examined DNA methylation patterns at promoters of endothelial cell (EC)-enriched genes during differentiation of mouse ES cells towards the EC. We have previously shown that eNOS, CD31, VE-cadherin and vWF, which have an EC-enriched pattern of gene expression are differentially methylated between EC and vascular smooth muscle cells. Given that differential promoter DNA methylation is functionally important we asked when these distinct patterns are established. Using the hanging drop method to differentiate ES cells, followed by FACS, we isolated early (EB-day4 VEGFR2-positive) and late (EB-day7 CD31-positive) endothelial progenitor cells. Though current paradigms suggest that lineage-restricted genes are methylated in ES cells, we show heterogeneous promoter DNA methylation. We show DNA demethylation at the CD31 promoter in EB-day 7 CD31-positive cells. In contrast, the eNOS promoter is still heavily methylated in EB-day 7 CD31 positive cells compared with murine EC where there is no DNA methylation.
机译:这项研究检查了小鼠ES细胞向EC分化过程中富含内皮细胞(EC)的基因启动子的DNA甲基化模式。先前我们已经表明,具有EC富集的基因表达模式的eNOS,CD31,VE-cadherin和vWF在EC和血管平滑肌细胞之间差异甲基化。鉴于差异启动子DNA甲基化在功能上很重要,因此我们询问何时建立这些不同的模式。使用悬滴法区分ES细胞,然后进行FACS,我们分离了早期(EB-day4 VEGFR2阳性)和晚期(EB-day7 CD31阳性)内皮祖细胞。尽管目前的范例表明,沿袭限制基因在ES细胞中被甲基化,但我们显示了异源启动子DNA甲基化。我们在EB天7 CD31阳性细胞中的CD31启动子处显示DNA脱甲基。相比之下,与没有DNA甲基化的鼠EC相比,在EB天7 CD31阳性细胞中eNOS启动子仍被高度甲基化。

著录项

  • 作者

    Kop, Anna.;

  • 作者单位

    University of Toronto (Canada).;

  • 授予单位 University of Toronto (Canada).;
  • 学科 Biology Molecular.
  • 学位 M.Sc.
  • 年度 2011
  • 页码 103 p.
  • 总页数 103
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

  • 入库时间 2022-08-17 11:45:24

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