[3'-->5'-exonucleases of the rat liver and the correction of replication errors].

N V Beliakova, N E Kleĭner, T P Kravetskaia, O K Legina, S N Naryzhnyĭ, F V Perrino, I V Shevelev, V M Krutiakov
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引用次数: 0

Abstract

Mammalian nuclear DNA polymerases alpha and beta are lack of the proofreading 3'-->5' exonucleolytic activity. 40 and 50 kDa 3'-->5' exonucleases were isolated from rat liver. The exonucleases were shown to excise mismatched nucleotides from poly[d(A--T)] template 10 and 2 fold faster than matched ones. The addition of either exonuclease to DNA polymerase alpha from rat liver or calf thymus 5-10 times increased the accuracy of reproduction of primed DNA from bacteriophage phi X174 amber 3, values of exonuclease and DNA polymerase activities being approximately equal. The exonuclease activity surpasses the DNA polymerase one by an order of magnitude in chromatin and nuclear membrane. These data, taken together, are indicative of potent proofreading into hepatocytes.

[3'- >5'-大鼠肝脏外切酶和复制错误的纠正]。
哺乳动物核DNA聚合酶α和β缺乏校对3'- >5'的核外溶活性。从大鼠肝脏中分离到40和50 kDa 3'- >5'外切酶。结果表明,外切酶从poly[d(A—T)]模板中去除不匹配的核苷酸的速度比匹配的快10倍和2倍。在大鼠肝脏或小牛胸腺DNA聚合酶α中加入5-10倍的外切酶,可提高噬菌体phi X174琥珀3引物DNA的复制精度,外切酶和DNA聚合酶的活性值大致相等。外切酶在染色质和核膜上的活性比DNA聚合酶高一个数量级。这些数据加在一起,表明对肝细胞的有效校对。
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