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Imprinting regulation of the murine Meg1/Grb10 and human GRB10 genes; roles of brain-specific promoters and mouse-specific CTCF-binding sites

机译:小鼠Meg1 / Grb10和人类GRB10基因的印迹调控;特异性启动子和小鼠特异性CTCF结合位点的作用

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The imprinted mouse gene Meg1/Grb10 is expressed from maternal alleles in almost all tissues and organs, except in the brain, where it is expressed biallelically, and the paternal allele is expressed preferentially in adulthood. In contrast, the human GRB10 gene shows equal biallelic expression in almost all tissues and organs, while it is almost always expressed paternally in the fetal brain. To elucidate the molecular mechanisms of the complex imprinting patterns among the different tissues and organs of humans and mice, we analyzed in detail both the genomic structures and tissue-specific expression profiles of these species. Experiments using 5'-RACE and RT-PCR demonstrated the existence in both humans and mice of novel brain-specific promoters, in which only the paternal allele was active. The promoters were located in the primary differentially methylated regions. Interestingly, CTCF-binding sites were found only in the mouse promoter region where CTCF showed DNA methylation-sensitive binding activity. Thus, the insulator function of CTCF might cause reciprocal maternal expression of the Meg1/Grb10 gene from another upstream promoter in the mouse, whereas the human upstream promoter is active in both parental alleles due to the lack of the corresponding insulator sequence in this region.
机译:印记的小鼠基因Meg1 / Grb10在几乎所有组织和器官中都由母体等位基因表达,除了大脑中以双等位基因表达的基因外,父本等位基因优先在成年期表达。相比之下,人类GRB10基因在几乎所有组织和器官中均显示相同的双等位基因表达,而它几乎总是在胎脑中父系表达。为了阐明人类和小鼠不同组织器官之间复杂印迹模式的分子机制,我们详细分析了这些物种的基因组结构和组织特异性表达谱。使用5'-RACE和RT-PCR进行的实验证明,在人类和小鼠中都存在新的大脑特异性启动子,其中只有父亲等位基因是活跃的。启动子位于主要的差异甲基化区域。有趣的是,仅在小鼠启动子区域发现了CTCF结合位点,其中CTCF显示了DNA甲基化敏感的结合活性。因此,CTCF的绝缘子功能可能会导致小鼠中另一个上游启动子的Meg1 / Grb10基因在母体中相互表达,而人上游启​​动子在两个亲本等位基因中都具有活性,因为该区域缺少相应的绝缘子序列。

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