Bisulfite genomic sequencing-derived methylation profile of the Xist gene throughout early mouse development

被引:52
作者
McDonald, LE
Paterson, CA
Kay, GF
机构
[1] Queensland Inst Med Res, Joint Expt Oncol Program, QCF Transgen Lab, Brisbane, Qld 4029, Australia
[2] Univ Queensland, Brisbane, Qld 4029, Australia
基金
澳大利亚研究理事会;
关键词
D O I
10.1006/geno.1998.5570
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Differential epigenetic modification by methylation of CpG; dinucleotides is a candidate mechanism that may identify the alleles of imprinted genes and result in monoallelic expression of either the maternal or the paternal allele. Determination of the allelic methylation status of imprinted genes in the gametes and during early development is constrained by the limiting quantities of genomic DNA available from these early developmental stages. To circumvent this problem we have used bisulfite genomic sequencing to determine the allelic methylation status of the minimal promoter and a l-kb region within the Xist gene during preimplantation development. We find that the parental Xist alleles are not differentially methylated in these regions. Our findings are discussed in the context of previous conflicting data obtained using methylation-sensitive restriction enzyme digestion followed by PCR amplification to assay for methylation. (C) 1998 Academic Press.
引用
收藏
页码:379 / 386
页数:8
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