Wang Y H, Griffith J D
Lineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill 27599-7295, USA.
Proc Natl Acad Sci U S A. 1996 Aug 20;93(17):8863-7. doi: 10.1073/pnas.93.17.8863.
Nucleosomes, the basic structural elements of chromosomes, consist of 146 bp of DNA coiled around an octamer of histone proteins, and their presence can strongly influence gene expression. Considerations of the anisotropic flexibility of nucleotide triplets containing 3 cytosines or guanines suggested that a [5'(G/C)3 NN3']n motif might resist wrapping around a histone octamer. To test this, DNAs were constructed containing a 5'-CCGNN-3' pentanucleotide repeat with the Ns varied. Using in vitro nucleosome reconstitution and electron microscopy, a plasmid with 48 contiguous CCGNN repeats strongly excluded nucleosomes in the repeat region. Competitive reconstitution gel retardation experiments using DNA fragments containing 12, 24, or 48 CCGNN repeats showed that the propensity to exclude nucleosomes increased with the length of the repeat. Analysis showed that a 268-bp DNA containing a (CCGNN)48 block is 4.9 +/- 0.6-fold less efficient in nucleosome assembly than a similar length pUC19 fragment and approximately 78-fold less efficient than a similar length (CTG)n sequence, based on results from previous studies. Computer searches against the GenBank database for matches with a [(G/C)3NN]48 sequence revealed numerous examples that frequently were present in the control regions of "TATA-less" genes, including the human ETS-2 and human dihydrofolate reductase genes. In both cases the (G/C)3NN repeat, present in the promoter region, co-maps with loci previously shown to be nuclease hypersensitive sites.
核小体是染色体的基本结构元件,由146个碱基对的DNA缠绕在组蛋白八聚体上组成,其存在会强烈影响基因表达。对含有3个胞嘧啶或鸟嘌呤的核苷酸三联体的各向异性柔韧性的考虑表明,[5'(G/C)3 NN3']n基序可能会抵抗围绕组蛋白八聚体的缠绕。为了验证这一点,构建了含有5'-CCGNN-3'五核苷酸重复序列且N可变的DNA。通过体外核小体重组和电子显微镜观察,一个具有48个连续CCGNN重复序列的质粒在重复区域强烈排斥核小体。使用含有12、24或48个CCGNN重复序列的DNA片段进行的竞争性重组凝胶阻滞实验表明,排斥核小体的倾向随重复序列长度的增加而增加。分析表明,根据先前研究的结果,一个含有(CCGNN)48片段的268碱基对DNA在核小体组装中的效率比类似长度的pUC19片段低4.9 +/- 0.6倍,比类似长度的(CTG)n序列低约78倍。在GenBank数据库中对与[(G/C)3NN]48序列匹配的计算机搜索揭示了许多实例,这些实例经常出现在“无TATA”基因的调控区域,包括人类ETS-2基因和人类二氢叶酸还原酶基因。在这两种情况下,启动子区域中存在的(G/C)3NN重复序列与先前显示为核酸酶超敏位点的基因座共定位。