Drew H R, Weeks J R, Travers A A
EMBO J. 1985 Apr;4(4):1025-32. doi: 10.1002/j.1460-2075.1985.tb03734.x.
We have examined the influence of negative supercoiling on the DNA structure of a bacterial promoter (tyrT from Escherichia coli), the transcriptional activity of which is strongly enhanced by torsional stress in vitro. Certain regions of this promoter become sensitive to digestion by single-strand-specific S1 nuclease as a consequence of negative superhelicity. These regions occur with high frequency (1 per 30-50 bp) and are normally centered on a TpA doublet. The major positions of cleavage are located in and around the -10 sequence TATGATG, the unwinding of which is a prerequisite for gene expression. An apparently trivial change in the -10 sequence from TATGATG to TATGAAG reduces both transcriptional activity and S1 nuclease sensitivity at least 10-fold. Thus the nuclease sensitivity of the promoter correlates strongly with its biological function; and both of these phenomena correlate with certain sequence-dependent structural properties of the DNA.
我们研究了负超螺旋对细菌启动子(来自大肠杆菌的tyrT)DNA结构的影响,该启动子的转录活性在体外会因扭转应力而显著增强。由于负超螺旋,该启动子的某些区域对单链特异性S1核酸酶的消化变得敏感。这些区域出现的频率很高(每30 - 50个碱基对中有1个),且通常以TpA双峰为中心。切割的主要位置位于-10序列TATGATG及其周围,该序列的解旋是基因表达的前提条件。-10序列从TATGATG到TATGAAG的一个明显微小变化,使转录活性和S1核酸酶敏感性至少降低了10倍。因此,启动子的核酸酶敏感性与其生物学功能密切相关;并且这两种现象都与DNA的某些序列依赖性结构特性相关。