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单亲胎儿中印迹基因亲本特异性表达的破坏。

Disruption of parental-specific expression of imprinted genes in uniparental fetuses.

作者信息

Ogawa Hidehiko, Wu Qiong, Komiyama Junichi, Obata Yayoi, Kono Tomohiro

机构信息

Department of Bioscience, Tokyo University of Agriculture, 1-1-1 Sakuragaoka, Tokyo 156-8502, Japan.

出版信息

FEBS Lett. 2006 Oct 2;580(22):5377-84. doi: 10.1016/j.febslet.2006.08.087. Epub 2006 Sep 12.

Abstract

In mammals, imprinted genes show parental origin-dependent expression based on epigenetic modifications called genomic imprinting (GI), which are established independently during spermatogenesis or oogenesis. Due to GI, uniparental fetuses never develop to term. To determine whether such expression of imprinted genes is maintained in uniparental mouse fetuses, we analyzed the expression of 20 paternally and 11 maternally expressed genes in androgenetic and parthenogenetic fetuses. Four genes of each type were expressed in both groups of fetuses. Furthermore, quantitative analysis showed that expression levels deviated from the presumed levels for some imprinted genes. These results suggest that mechanisms acting in trans between paternal and maternal alleles are involved in the appropriate expression of some imprinted genes.

摘要

在哺乳动物中,印记基因基于称为基因组印记(GI)的表观遗传修饰呈现亲本来源依赖性表达,这些修饰在精子发生或卵子发生过程中独立建立。由于基因组印记,单亲胎儿无法发育至足月。为了确定印记基因的这种表达在单亲小鼠胎儿中是否得以维持,我们分析了孤雄和孤雌胎儿中20个父源表达基因和11个母源表达基因的表达情况。每组胎儿中各有4个基因表达。此外,定量分析表明,一些印记基因的表达水平偏离了预期水平。这些结果表明,父本和母本等位基因之间的反式作用机制参与了一些印记基因的正常表达。

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