S1 nuclease sensitivity to cis- and trans-diamminedichloroplatinum(II) modified DNAS: influence of (G+C) content and nucleotide sequence.
S1 nuclease sensitivity to cis- and trans-diamminedichloroplatinum(II) modified DNAS: influence of (G+C) content and nucleotide sequence.
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S1 核酸酶对顺式和反式二氯二氨铂 (II) 修饰的 DNAS 的敏感性:(GC) 含量和核苷酸序列的影响。
DOI:
10.1016/0006-291x(84)91562-6
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发表时间:
1984
影响因子:
3.1
通讯作者:
Vincent J. Capponi
中科院分区:
文献类型:
--
作者:
W. Scovell;Vincent J. Capponi
The sensitivity of S1 nuclease to cis- and trans-(NH3)2PtCl2modified DNAs is examined as a function of (1) the level of cis- and trans-(NH3)2PtCl2bound, (2) the % (G+C) content in DNA from different sources and (3) the sequence dependence in poly(dG).poly(dC) and poly(dG-dC).poly(dG-dC). The extent of DNA digested increases with increasing levels of either isomer and is inversely influenced by the % (G+C) content of the DNA. However, the difference in the extent of digestion between the cis-and trans-(NH3)2PtCl2modified DNAs at equivalent levels of bound isomer follows the order, calf-thymus > M. lysodeikticus > poly(dG-dC).poly(dG-dC). While there is virtually no difference in the digestion profiles for poly(dG-dC).poly(dG-dC) modified with the two isomers, there is a striking difference in the extent of digestion between cis- and trans-(NH3)2PtCl2modified poly(dG).poly(dC). These results are discussed in light of (1) the possible modes of binding for cis-(NH3)2PtCl2, (2) previously reported findings on modified DNA and (3) possible implications for modifications in cellular chromatin.
影响因子:
14.9
作者:
Royer-Pokora,B;Gordon,LK;Haseltine,WA
通讯作者:
Haseltine,WA