Dlk1-Dio3印记区域在胚胎发育、细胞重编程和遗传疾病过程中起重要作用。Meg8-DMR是Dlk1-Dio3印记区域内第一个被发现的母本甲基化的差异甲基化区，在着床前后的胚胎发育中呈现去甲基化和重新甲基化的动态变化过程，其生物学功能尚不清楚。本课题基于CRISPR/Cas9基因编辑技术，构建Meg8-DMR缺失细胞系和敲除小鼠模型。通过细胞系和不同发育阶段胚胎高通量的表达谱分析和全基因组范围内DNA甲基化谱分析，以及ChIP实验和依赖于CTCF的绝缘子活性研究，结合细胞行为和小鼠表型分析，探索差异甲基化区Meg8-DMR参与Dlk1-Dio3印记区域内的印记形成和调控的分子机制，揭示Meg8-DMR在胚胎发育过程中的生物学功能。本课题将进一步阐明Dlk1-Dio3印记区域的转录调控机制，并为今后发育生物学研究、细胞重编程、器官发育的调控及遗传性疾病的评估诊断提供新的分子靶标。

The Dlk1-Dio3 imprinted domain plays crucial roles in embryonic development, cell reprogramming and genetic diseases. As the fist detected maternal methylated region located in Dlk1-Dio3 imprinted domain, Meg8-DMR shows the dynamic process with dymethylation and de novo methylation, but its biological functions still remain unclear. Based on the CRISPR/Cas9 genome editing technique, Meg8-DMR deletion cell line and knockout mouse model were constructed. Through the genome-wide expression profiling and DNA methylation profiling analysis of cell lines and different embryonic developmental stages by high-throughput sequencing, as well as ChIP experiments and the CTCF-dependent insulator activity studies, combined with the analysis of cell behavior and mouse phenotype, detect the formation and the regulatory mechanism of the Dlk1-Dio3 imprinted domain which the differentially methylated region Meg8-DMR participate in, and uncover the biological functions of the differentially methylated region Meg8-DMR during the embryonic development. This study will further clarify the transcriptional regulation mechanism of the Dlk1-Dio3 imprinted domain, and provide new molecular targets for the future developmental biology research, cell reprogramming, the regulation of organ development and the evaluation of genetic diseases.