Painter R B, Young B R, Kapp L N
Laboratory of Radiobiology and Environmental Health, University of California, San Francisco 94143.
Cancer Res. 1987 Nov 1;47(21):5595-9.
Previous reports have suggested that transient inhibition of DNA synthesis by chemicals or ultraviolet light causes some of the DNA to replicate more than once in one cell cycle, i.e., that it induces overreplication of DNA. The data that led to this suggestion were obtained from cesium chloride equilibrium density gradient analyses, in which cells were incubated with bromodeoxyuridine so that the DNA synthesized after incubation with the inhibitor could be densitometrically separated from the DNA that had been radioactively labeled before incubation with the inhibitor. An unresolved problem with these analyses was that the data also suggested that overreplication must have occurred in control cells, i.e., those not incubated with an inhibitor of DNA synthesis. We show here that the latter result is probably due to an artifact of cesium chloride equilibrium density gradient analysis, probably because of nonspecific trapping of DNA in regions of the gradients where there are large amounts of DNA. We also used another protocol that avoids this artifact; with this protocol any overreplicated DNA would be found where heavy-heavy DNA bands and nonspecific trapping cannot occur. When this protocol was used there was no evidence that transient inhibition of DNA synthesis induces overreplication of DNA.
先前的报告表明,化学物质或紫外线对DNA合成的短暂抑制会导致部分DNA在一个细胞周期内复制不止一次,即诱导DNA的过度复制。得出这一结论的数据来自氯化铯平衡密度梯度分析,在该分析中,细胞用溴脱氧尿苷进行孵育,这样在与抑制剂孵育后合成的DNA就可以通过密度测定法与在与抑制剂孵育前已进行放射性标记的DNA区分开来。这些分析中一个尚未解决的问题是,数据还表明过度复制肯定也发生在对照细胞中,即那些未与DNA合成抑制剂孵育的细胞。我们在此表明,后一结果可能是由于氯化铯平衡密度梯度分析的假象,可能是因为DNA在梯度中DNA含量高的区域发生了非特异性滞留。我们还采用了另一种避免这种假象的方法;使用这种方法时,任何过度复制的DNA都会出现在不可能出现重-重DNA条带和非特异性滞留的地方。当采用这种方法时,没有证据表明DNA合成的短暂抑制会诱导DNA的过度复制。