Analysis of a four generation family reveals the widespread sequence-dependent maintenance of allelic DNA methylation in somatic and germ cells.
Analysis of a four generation family reveals the widespread sequence-dependent maintenance of allelic DNA methylation in somatic and germ cells.
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对四代家族的分析揭示了体细胞和生殖细胞中等位基因 DNA 甲基化的广泛序列依赖性维持。
DOI:
10.1038/srep19260
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发表时间:
2016
期刊:
影响因子:
--
通讯作者:
Cai Zhiming
中科院分区:
文献类型:
--
作者:
Tang Aifa;Huang Yi;Li Zesong;Wan Shengqing;Mou Lisha;Yin Guangliang;Li Ning;Xie Jun;Xia Yudong;Li Xianxin;Luo Liya;Zhang Junwen;Chen Shen;Wu Song;Sun Jihua;Sun Xiaojuan;Jiang Zhimao;Chen Jing;Li Yingrui;Wang Jian;Wang Jun;Cai Zhiming
Differential methylation of the homologous chromosomes, a well-known mechanism leading to genomic imprinting and X-chromosome inactivation, is widely reported at the non-imprinted regions on autosomes. To evaluate the transgenerational DNA methylation patterns in human, we analyzed the DNA methylomes of somatic and germ cells in a four-generation family. We found that allelic asymmetry of DNA methylation was pervasive at the non-imprinted loci and was likely regulated bycis-acting genetic variants. We also observed that the allelic methylation patterns for the vast majority of thecis-regulated loci were shared between the somatic and germ cells from the same individual. These results demonstrated the interaction between genetic and epigenetic variations and suggested the possibility of widespread sequence-dependent transmission of DNA methylation during spermatogenesis.