Costlow N A, Simon J A, Lis J T
Nature. 1985;313(5998):147-9. doi: 10.1038/313147a0.
Nuclease-hypersensitive sites in chromatin exist at the 5' side of many eukaryotic genes. To gain some understanding of the molecular basis of these hypersensitive sites, we have now examined the pair of sites upstream of the Drosophila hsp70 gene in a series of plasmids that contain deletions in the hypersensitive region and have been transformed into yeast cells. Hypersensitive sites 5' to a Drosophila hsp70 gene are preserved when this gene is introduced into yeast by transformation. We find that a yeast strain containing a plasmid in which the deletion extends through the first hypersensitive site still displays the normal pair of hypersensitive sites, so DNA sequences over which the first hypersensitive site is centred are not required for hypersensitivity at this position and the site can form over a foreign DNA sequence juxtaposed against this deletion end point. Deletions progressing further into the region bracketed by the pair of 5' hypersensitive sites eliminate the first hypersensitive site and alter the downstream site. We propose that the hypersensitive sites are generated through the binding of a protein that renders flanking sequences more accessible to nucleases, perhaps by preventing normal chromatin packaging.
染色质中的核酸酶超敏位点存在于许多真核基因的5'端。为了对这些超敏位点的分子基础有一些了解,我们现在研究了果蝇hsp70基因上游的一对位点,这些位点位于一系列质粒中,这些质粒在超敏区域存在缺失并且已被转化到酵母细胞中。当通过转化将果蝇hsp70基因导入酵母时,该基因5'端的超敏位点得以保留。我们发现,含有一个质粒的酵母菌株,其中缺失延伸至第一个超敏位点,仍然显示出正常的一对超敏位点,因此第一个超敏位点所围绕的DNA序列对于该位置的超敏性并非必需,并且该位点可以在与该缺失端点并列的外源DNA序列上形成。进一步进入由一对5'超敏位点所包围区域的缺失会消除第一个超敏位点并改变下游位点。我们提出,超敏位点是通过一种蛋白质的结合而产生的,这种蛋白质使侧翼序列更容易被核酸酶接近,也许是通过阻止正常的染色质包装来实现的。