Gruskin E A, Rich A
Department of Biology, Massachusetts Institute of Technology, Cambridge 02139.
Biochemistry. 1993 Mar 9;32(9):2167-76. doi: 10.1021/bi00060a007.
During replication and transcription, the SV40 control region is subjected to significant levels of DNA unwinding. There are three, alternating purine-pyrimidine tracts within this region that can adopt the Z-DNA conformation in response to negative superhelix density: a single copy of ACACACAT and two copies of ATGCATGC. Since the control region is essential for both efficient transcription and replication, B-DNA to Z-DNA transitions in these vital sequence tracts may have significant biological consequences. We have synthesized DNA minicircles to detect B-DNA to Z-DNA transitions in the SV40 enhancer, and to determine the negative superhelix density required to stabilize the Z-DNA. A variety of DNA sequences, including the entire SV40 enhancer and the two segments of the enhancer with alternating purine-pyrimidine tracts, were incorporated into topologically relaxed minicircles. Negative supercoils were generated, and the resulting topoisomers were resolved by electrophoresis. Using an anti-Z-DNA Fab and an electrophoretic mobility shift assay, Z-DNA was detected in the enhancer-containing minicircles at a superhelix density of -0.05. Fab saturation binding experiments demonstrated that three, independent Z-DNA tracts were stabilized in the supercoiled minicircles. Two other minicircles, each with one of the two alternating purine-pyrimidine tracts, also contained single Z-DNA sites. These results confirm the identities of the Z-DNA-forming sequences within the control region. Moreover, the B-DNA to Z-DNA transitions were detected at superhelix densities observed during normal replication and transcription processes in the SV40 life cycle.
在复制和转录过程中,SV40控制区域会经历显著程度的DNA解旋。该区域内有三个交替的嘌呤-嘧啶序列,可响应负超螺旋密度而采用Z-DNA构象:一个ACACACAT拷贝和两个ATGCATGC拷贝。由于控制区域对于高效转录和复制都至关重要,这些重要序列中的B-DNA向Z-DNA转变可能会产生重大生物学后果。我们合成了DNA微环,以检测SV40增强子中B-DNA向Z-DNA的转变,并确定稳定Z-DNA所需的负超螺旋密度。包括整个SV40增强子以及具有交替嘌呤-嘧啶序列的增强子的两个片段在内的各种DNA序列被整合到拓扑松弛的微环中。产生负超螺旋,所得拓扑异构体通过电泳分离。使用抗Z-DNA Fab和电泳迁移率变动分析,在超螺旋密度为-0.05时,在含增强子的微环中检测到Z-DNA。Fab饱和结合实验表明,在超螺旋微环中有三个独立的Z-DNA序列被稳定。另外两个微环,每个都含有两个交替嘌呤-嘧啶序列中的一个,也含有单个Z-DNA位点。这些结果证实了控制区域内形成Z-DNA的序列的身份。此外,在SV40生命周期的正常复制和转录过程中观察到的超螺旋密度下检测到了B-DNA向Z-DNA的转变。