Zenkova M A, Karpova G G, Levina A S
Mol Biol (Mosk). 1989 Jul-Aug;23(4):1057-66.
16S rRNA chain was cleaved by RNase H within covalent adduct with a 2',3'-0-[4-N-(2-chloroethyl)-N-methylamino]benzylidene derivative of d(pACCTTGTT)rA. It was shown that no less than 50% of cleavage occurs at the 1498-1506 site. The selectivity of alkylation and correspondingly the cleavage by RNase H, at this site practically does not increase when RNA was alkylated to a low extent, and also when a small excess of the reagent in respect to rRNA was used.
16S rRNA链在与d(pACCTTGTT)rA的2',3'-O-[4-N-(2-氯乙基)-N-甲基氨基]亚苄基衍生物形成的共价加合物内被RNase H切割。结果表明,至少50%的切割发生在1498-1506位点。当RNA烷基化程度较低时,以及相对于rRNA使用少量过量试剂时,该位点的烷基化选择性以及相应的RNase H切割实际上并没有增加。