D'iachenko L B, Chenchik A A, Khaspekov G L, Tatarenko A O, Bibilashvili R Sh
Mol Biol (Mosk). 1994 Sep-Oct;28(5):1014-27.
We have studied the efficiency of DNA synthesis catalyzed by M-MLV reverse transcriptase or Thermus aquaticus DNA polymerase for primers (4-17 nucleotides long) either completely matched or possessing a single mismatched base pair at all possible positions in the primer. It has been shown that DNA synthesis efficiency depends not only on the position of mismatched base pair but on the length and primary structure of the primer. The enzyme, template, and primer concentrations determine the relative level of mismatched DNA synthesis.
我们研究了莫洛尼氏鼠白血病病毒(M-MLV)逆转录酶或嗜热栖热菌DNA聚合酶催化的DNA合成效率,所用引物长度为4至17个核苷酸,这些引物要么与模板完全匹配,要么在引物的所有可能位置都有一个错配碱基对。结果表明,DNA合成效率不仅取决于错配碱基对的位置,还取决于引物的长度和一级结构。酶、模板和引物的浓度决定了错配DNA合成的相对水平。