Povirk L F, Han Y H, Steighner R J
Department of Pharmacology and Toxicology, Medical College of Virginia, Virginia Commonwealth University, Richmond 23298.
Biochemistry. 1989 Jul 11;28(14):5808-14. doi: 10.1021/bi00440a016.
In order to examine the structure of bleomycin-induced DNA double-strand breaks, defined-sequence DNA was labeled in each strand at a single restriction site and treated with bleomycin. Various double-stranded fragments resulting from bleomycin-induced double-strand breaks were isolated, denatured, and run on sequencing gels to determine the sites of cleavage in each strand. For virtually every double-strand break, the cleavage site in one strand was a pyrimidine in a G-Py sequence, reflecting a specificity similar to that of bleomycin-induced single-strand cleavage. However, the cleavage site in the complementary strand was seldom a G-Py sequence, and was usually a site where single-strand cleavage was infrequent. When the sequence at the double-strand break was G-Py-Py', the break at Py was usually accompanied by a break at the base directly opposite Py, resulting in blunt ends. When the sequence was G-Py-Pu, the break at Py was usually accompanied by a break at the base opposite Pu, resulting in single-base 5' extensions. Double-strand breaks with 3' extensions, such as would result from cleavage of two C residues in a self-complementary G-C sequence, were conspicuously absent. These data provide further evidence that bleomycin-induced double-strand breaks do not result from coincidence of independent site-specific single-strand breaks.(ABSTRACT TRUNCATED AT 250 WORDS)
为了研究博来霉素诱导的DNA双链断裂的结构,在单一切割位点对定义序列的DNA每条链进行标记,并用博来霉素处理。分离出由博来霉素诱导的双链断裂产生的各种双链片段,使其变性,并在测序凝胶上进行电泳,以确定每条链上的切割位点。对于几乎每一个双链断裂,一条链上的切割位点是G-Py序列中的嘧啶,这反映出与博来霉素诱导的单链切割相似的特异性。然而,互补链上的切割位点很少是G-Py序列,通常是单链切割不常见的位点。当双链断裂处的序列为G-Py-Py'时,Py处的断裂通常伴随着与Py直接相对的碱基处的断裂,从而产生平端。当序列为G-Py-Pu时,Py处的断裂通常伴随着与Pu相对的碱基处的断裂,从而产生单碱基5'延伸。明显不存在由自互补G-C序列中的两个C残基切割产生的具有3'延伸的双链断裂。这些数据进一步证明,博来霉素诱导的双链断裂并非由独立的位点特异性单链断裂的巧合所致。(摘要截短至250字)