DNA methylation and differentiation: silencing, upregulation and modulation of gene expression

被引:165
作者
Ehrlich, Melanie [1 ,2 ]
Lacey, Michelle [3 ,4 ,5 ]
机构
[1] Tulane Canc Ctr, Hayward Human Genet Program, New Orleans, LA 70112 USA
[2] Tulane Hlth Sci Ctr, Ctr Bioinformat & Genom, New Orleans, LA 70112 USA
[3] Tulane Canc Ctr, New Orleans, LA 70112 USA
[4] Tulane Hlth Sci Ctr, Dept Math, New Orleans, LA 70112 USA
[5] Tulane Univ, New Orleans, LA 70112 USA
关键词
alternative splicing; CTCF; DNA methylation; enhancer; epigenetic; HOX gene; LSP1; skeletal muscle; TBX1; transcription termination; CPG METHYLATION; MYOGENIC DIFFERENTIATION; CONSERVED ROLE; BINDING-SITES; MESSENGER-RNA; MUSCLE CELLS; STEM-CELLS; HOX GENES; DEMETHYLATION; CHROMATIN;
D O I
10.2217/epi.13.43
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Differentiation-related DNA methylation is receiving increasing attention, partly owing to new, whole-genome analyses. These revealed that cell type-specific differential methylation in gene bodies is more frequent than in promoters. We review new insights into the functionality of DNA methylation during differentiation, with emphasis on the methylomes of myoblasts, myotubes and skeletal muscle versus non-muscle samples. Biostatistical analyses of data from reduced representation bisulfite sequencing are discussed. Lastly, a model is presented for how promoter and intragenic DNA hypermethylation affect gene expression, including increasing the efficiency of polycomb silencing at some promoters, downmodulating other promoters rather than silencing them, counteracting enhancers with heterologous specificity, altering chromatin conformation by inhibiting the binding of CTCF, modulating mRNA transcript levels by inhibiting overlapping promoters of noncoding RNA genes or by regulating the use of alternative mRNA promoters, modulating transcription termination, regulating alternative splicing and acting as barriers to the spread of activating chromatin.
引用
收藏
页码:553 / 568
页数:16
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