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Differential gene expression of murine blastocyst stage embryos and murine embryonic stem cells.

机译:小鼠胚泡期胚胎和小鼠胚胎干细胞的差异基因表达。

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摘要

Scope and method of study. Embryonic stem cells (ESC), derived from cultured blastocyst embryos, have the potential to provide insight into developmental and medical issues. The cellular transition, however, from blastocyst to ESC has not been well characterized. The purpose of this study was to identify transcriptional differences between blastocysts and ESC through use of suppression subtraction hybridization (SSH) in murine CD1 blastocyst and 129SvEv ESC. Comparisons between the following groups: blastocyst - blastocyst, trophectoderm - blastocyst, blastocyst - ESC, and ESC - fibroblast feeder cell, resulted in the cloning, sequencing, and identification of uniquely expressed sequences. The second objective was to compare expression levels of three selected transcripts through real time PCR in blastocysts, 129SvEv ESC, C57BL/6 ESC, and fibroblast feeder cells.; Findings and conclusions. Using SSH, 33 unique clones were identified and 10 had strong ribosomal homologies while 23 had either gene specific homologies or else were unknown. Prdx1, Ywahz, and Vdacs3 were analyzed through real time PCR. For Prdx1, fibroblast feeder cells had the lowest expression level, blastocysts had a 4.81 fold increase, 129SvEv ESC had a 7.51 fold increase, and the C57BL/6 ESC showed a 27.28 fold increase. Expression levels were significantly different between the blastocyst and C57BL/6 samples as well as the fibroblast feeder cells and both ESC samples based on DeltaCT statistical analysis. For Ywhaz, the fibroblast feeder sample showed the lowest expression level, blastocysts had a 7.65 fold increase, 129SvEv ESC showed a 6.49 fold increase, and C57BL/6 ESC showed a 16.56 fold difference. The two ESC values were significantly different as was the fibroblast feeder cell value from all other samples. For Vdacs3, the blastocyst sample had the lowest level of expression, fibroblast feeder cells had a 2.16 fold difference, 129SvEv ESC had a 68.07 fold difference, and C57BL/6 ESC had a 161.04 fold difference. Statistically, the blastocyst sample was different from both of the ESC samples and the fibroblast sample from either ESC sample. Prdx1 and Vdacs3 both demonstrated significant upregulation in comparison between blastocyst stage embryos and ESC and function to enhance cell survival and continued cell reproduction.
机译:研究范围和方法。胚胎干细胞(ESC)来源于培养的胚泡胚胎,具有提供有关发育和医学问题的见识的潜力。然而,从囊胚到ESC的细胞过渡尚未被很好地表征。这项研究的目的是通过在小鼠CD1囊胚和129SvEv ESC中使用抑制扣除杂交(SSH)来鉴定囊胚和ESC之间的转录差异。比较以下两组:胚泡-胚泡,滋养外胚层-胚泡,胚泡-ESC和ESC-成纤维细胞饲养细胞,可以克隆,测序和鉴定独特表达的序列。第二个目的是通过实时PCR比较三种选择的转录本在胚泡,129SvEv ESC,C57BL / 6 ESC和成纤维细胞饲养细胞中的表达水平。结论和结论。使用SSH,鉴定出33个独特的克隆,其中10个具有强核糖体同源性,而23个具有基因特异性同源性或未知。通过实时PCR分析Prdx1,Ywahz和Vdacs3。对于Prdx1,成纤维细胞饲养细胞的表达水平最低,胚泡增加4.81倍,129SvEv ESC增加7.51倍,C57BL / 6 ESC增加27.28倍。基于DeltaCT统计分析,胚泡和C57BL / 6样本以及成纤维细胞饲养细胞和两个ESC样本之间的表达水平显着不同。对于Ywhaz,成纤维细胞饲养者样品显示最低的表达水平,胚泡增加7.65倍,129SvEv ESC显示增加6.49倍,C57BL / 6 ESC显示增加16.56倍。这两个ESC值与所有其他样品的成纤维细胞饲养细胞值明显不同。对于Vdacs3,胚泡样品的表达水平最低,成纤维细胞饲养细胞的差异为2.16倍,129SvEv ESC的差异为68.07倍,C57BL / 6 ESC的差异为161.04倍。从统计学上讲,胚泡样品不同于两种ESC样品以及两种ESC样品中的成纤维细胞样品。 Prdx1和Vdacs3都显示出胚泡期胚胎和ESC之间的显着上调,并且具有增强细胞存活和持续细胞繁殖的功能。

著录项

  • 作者

    Myer, Sarah E.;

  • 作者单位

    Oklahoma State University.$bBiochemistry & Molecular Biology.;

  • 授予单位 Oklahoma State University.$bBiochemistry & Molecular Biology.;
  • 学科 Biology Molecular.; Biology Genetics.
  • 学位 Ph.D.
  • 年度 2007
  • 页码 168 p.
  • 总页数 168
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 分子遗传学;遗传学;
  • 关键词

  • 入库时间 2022-08-17 11:39:52

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