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首页> 外文期刊>The Journal of Reproduction and Development >Deletion of conserved sequences in IG-DMR at Dlk1-Gtl2 locus suggests their involvement in expression of paternally expressed genes in mice
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Deletion of conserved sequences in IG-DMR at Dlk1-Gtl2 locus suggests their involvement in expression of paternally expressed genes in mice

机译:在Dlk1-Gtl2基因座处删除IG-DMR中的保守序列,表明它们参与了小鼠中父本表达基因的表达

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摘要

Expression regulation of the Dlk1 - Dio3 imprinted domain by the intergenic differentially methylated region (IG-DMR) is essential for normal embryonic development in mammals. In this study, we investigated conserved IG-DMR genomic sequences in eutherians to elucidate their role in genomic imprinting of the Dlk1 - Dio3 domain. Using a comparative genomics approach, we identified three highly conserved sequences in IG-DMR. To elucidate the functions of these sequences in vivo , we generated mutant mice lacking each of the identified highly conserved sequences using the CRISPR/Cas9 system. Although mutant mice did not exhibit the gross phenotype, deletions of the conserved sequences altered the expression levels of paternally expressed imprinted genes in the mutant embryos without skewing imprinting status. These results suggest that the conserved sequences in IG-DMR are involved in the expression regulation of some of the imprinted genes in the Dlk1 - Dio3 domain.
机译:基因间差异甲基化区域(IG-DMR)对Dlk1-Dio3印迹域的表达调控对于哺乳动物的正常胚胎发育至关重要。在这项研究中,我们调查了欧洲人中保守的IG-DMR基因组序列,以阐明它们在Dlk1-Dio3域的基因组印迹中的作用。使用比较基因组学方法,我们在IG-DMR中鉴定了三个高度保守的序列。为了阐明这些序列在体内的功能,我们使用CRISPR / Cas9系统生成了缺少每种已鉴定的高度保守序列的突变小鼠。尽管突变小鼠没有表现出总体表型,但保守序列的缺失改变了突变体胚胎中父本表达的印迹基因的表达水平,而没有歪曲印迹状态。这些结果表明,IG-DMR中的保守序列参与了Dlk1-Dio3结构域中某些印迹基因的表达调控。

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