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种间小鼠杂交后代胎盘的DNA甲基化

DNA methylation in placentas of interspecies mouse hybrids.

作者信息

Schütt Sabine, Florl Andrea R, Shi Wei, Hemberger Myriam, Orth Annie, Otto Sabine, Schulz Wolfgang A, Fundele Reinald H

机构信息

Max-Planck-Institute for Molecular Genetics, 14195 Berlin, Germany.

出版信息

Genetics. 2003 Sep;165(1):223-8. doi: 10.1093/genetics/165.1.223.

Abstract

Interspecific hybridization in the genus Mus results in several hybrid dysgenesis effects, such as male sterility and X-linked placental dysplasia (IHPD). The genetic or molecular basis for the placental phenotypes is at present not clear. However, an extremely complex genetic system that has been hypothesized to be caused by major epigenetic changes on the X chromosome has been shown to be active. We have investigated DNA methylation of several single genes, Atrx, Esx1, Mecp2, Pem, Psx1, Vbp1, Pou3f4, and Cdx2, and, in addition, of LINE-1 and IAP repeat sequences, in placentas and tissues of fetal day 18 mouse interspecific hybrids. Our results show some tendency toward hypomethylation in the late gestation mouse placenta. However, no differential methylation was observed in hyper- and hypoplastic hybrid placentas when compared with normal-sized littermate placentas or intraspecific Mus musculus placentas of the same developmental stage. Thus, our results strongly suggest that generalized changes in methylation patterns do not occur in trophoblast cells of such hybrids.

摘要

小家鼠属中的种间杂交会导致多种杂种发育异常效应,如雄性不育和X连锁胎盘发育异常(IHPD)。目前,胎盘表型的遗传或分子基础尚不清楚。然而,一个极其复杂的遗传系统被认为是由X染色体上的主要表观遗传变化引起的,并且已被证明是活跃的。我们研究了几种单基因(Atrx、Esx1、Mecp2、Pem、Psx1、Vbp1、Pou3f4和Cdx2)以及LINE-1和IAP重复序列在胚胎第18天小鼠种间杂交后代的胎盘和组织中的DNA甲基化情况。我们的结果显示,妊娠后期小鼠胎盘有一定程度的低甲基化倾向。然而,与正常大小的同窝胎盘或相同发育阶段的小家鼠种内胎盘相比,在增生性和发育不全的杂种胎盘中未观察到差异甲基化。因此,我们的结果强烈表明,此类杂种的滋养层细胞中不会发生甲基化模式的普遍变化。

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