Nightingale K, Wolffe A P
Laboratory of Molecular Embryology, NICHHD, National Institutes of Health, Bethesda, Maryland 20892.
J Biol Chem. 1995 Mar 3;270(9):4197-200. doi: 10.1074/jbc.270.9.4197.
We demonstrate that methylation of the 12 dinucleotide CpGs within a GC-rich DNA fragment containing a Xenopus borealis 5 S rRNA gene does not influence histone H1 binding to naked or nucleosomal 5 S DNA. Thus a simple mechanism in which histone H1 selectively associates with nucleosomes containing methylated CpG cannot explain the repressive effects of methylation on gene activity.
我们证明,在含有北方爪蟾5S rRNA基因的富含GC的DNA片段内,12个二核苷酸CpG的甲基化并不影响组蛋白H1与裸露或核小体形式的5S DNA的结合。因此,组蛋白H1选择性地与含有甲基化CpG的核小体结合这一简单机制,无法解释甲基化对基因活性的抑制作用。