Kladde M P, Simpson R T
Laboratory of Cellular and Developmental Biology, National Institutes of Health, Bethesda, MD 20892.
Proc Natl Acad Sci U S A. 1994 Feb 15;91(4):1361-5. doi: 10.1073/pnas.91.4.1361.
Escherichia coli Dam DNA methyltransferase can methylate genomic GATC sites when expressed in Saccharomyces cerevisiae. Others have observed changes in the level of methylation at specific sites and suggested that these changes are related to transcriptional state or chromosomal context. To test directly the influence of nucleosome location on the ability of Dam methyltransferase to modify GATC sites in chromatin, we analyzed minichromosomes containing precisely positioned nucleosomes in dam-expressing yeast strains. Levels of methylation at individual GATC sites were rigorously quantified by an oligonucleotide-probing procedure. Within the linker and adjacent 21 bp of nucleosome-associated DNA, GATC sites were highly methylated, whereas methylation was severely inhibited by histone-DNA contacts nearer to the nucleosomal pseudodyad. Other DNA-protein complexes also interfere with Dam methylation. These data are consistent with a model in which nucleosomes exert a repressive influence on the biological functions of DNA by restricting access of trans-acting factors to DNA.
大肠杆菌Dam DNA甲基转移酶在酿酒酵母中表达时可使基因组GATC位点发生甲基化。其他人观察到特定位点甲基化水平的变化,并认为这些变化与转录状态或染色体背景有关。为了直接测试核小体位置对Dam甲基转移酶修饰染色质中GATC位点能力的影响,我们分析了在表达dam的酵母菌株中含有精确定位核小体的微型染色体。通过寡核苷酸探测程序严格定量了各个GATC位点的甲基化水平。在连接区和与核小体相关的DNA相邻的21 bp内,GATC位点高度甲基化,而靠近核小体假二元体的组蛋白-DNA接触则严重抑制甲基化。其他DNA-蛋白质复合物也会干扰Dam甲基化。这些数据与一种模型一致,即核小体通过限制反式作用因子与DNA的接触对DNA的生物学功能产生抑制作用。