首页> 外文期刊>Developmental dynamics: an official publication of the American Association of Anatomists >Different molecular mechanisms underlie placental overgrowth phenotypes caused by interspecies hybridization, cloning, and Esx1 mutation.
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Different molecular mechanisms underlie placental overgrowth phenotypes caused by interspecies hybridization, cloning, and Esx1 mutation.

机译:种间杂交,克隆和Esx1突变引起胎盘过度生长表型的分子机制不同。

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摘要

To obtain a deeper insight into the genes and gene networks involved in the development of placentopathies, we have assessed global gene expression in three different models of placental hyperplasia caused by interspecies hybridization (IHPD), cloning by nuclear transfer, and mutation of the Esx1 gene, respectively. Comparison of gene expression profiles of approximately 13,000 expressed sequence tags (ESTs) identified specific subsets of genes with changed expression levels in IHPD, cloned, and Esx1 mutant placentas. Of interest, only one gene of known function and one EST of unknown function were found common to all three placentopathies; however, a significant number of ESTs were common to IHPD and cloned placentas. In contrast, only one gene was shared between IHPD and Esx1 mutant, and cloned and Esx1 mutant placentas, respectively. These genes common to different abnormal placental growth genotypes are likely to be important in the occurrence of placentopathy.
机译:为了更深入地了解胎盘病发展过程中涉及的基因和基因网络,我们评估了三种不同模式下由种间杂交(IHPD),核转移克隆和Esx1基因突变引起的胎盘增生的整体基因表达, 分别。比较大约13,000个表达的序列标签(EST)的基因表达谱,确定了在IHPD,克隆的和Esx1突变型胎盘中表达水平发生变化的特定基因子集。有趣的是,只有一种已知功能的基因和一种未知功能的EST被发现为所有三种胎盘疾病共有。但是,IHPD和克隆胎盘中有大量EST是共有的。相反,IHPD和Esx1突变体,克隆的Esx1突变体和胎盘分别只有一个基因。这些不同胎盘生长异常基因型共有的基因在胎盘病的发生中可能很重要。

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