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来自人淋巴细胞的DNA引发酶活性。引发DNA合成的寡核糖核苷酸的合成。

DNA primase activity from human lymphocytes. Synthesis of oligoribonucleotides that prime DNA synthesis.

作者信息

Tseng B Y, Ahlem C N

出版信息

J Biol Chem. 1982 Jul 10;257(13):7280-3.

PMID:7085624
Abstract

A fraction has been prepared from extracts of a human lymphoblastoid cell line that has properties of a mammalian DNA primase and also contains a DNA polymerase activity with unusual properties. With a variety of synthetic single-stranded DNA templates using rNTPs alone, the products consist of oligoribonucleotides of a restricted size range, primarily 7 to 9 nucleotides in length. Poly(dIT) is the most active template found thus far. The activity appears to have "relaxed" substrate/template complementarity requirements similar to those described previously for mammalian primase; poly(dIT) template with rATP alone results in synthesis of oligo(rA) of the same size as oligo(rAC) made when both rATP and rCTP are present. When dNTPs are added to the reaction, DNA is synthesized by extension of the oligoribonucleotide, which acts as primer. The DNA product appears in relatively discrete sizes that differ by approximately 8 nucleotides, with a large proportion of the product around 24 and 32 nucleotides. In addition to the relatively discrete size of its product, the DNA polymerase activity that utilizes the endogenously synthesized oligoribonucleotide primer on poly(dIT) template differs from polymerase alpha in its resistance to aphidicolin and low Km for dNTP.

摘要

已从人淋巴母细胞系提取物中制备出一种组分,该组分具有哺乳动物DNA引发酶的特性,并且还含有具有异常特性的DNA聚合酶活性。使用仅含rNTPs的多种合成单链DNA模板时,产物由大小受限的寡核糖核苷酸组成,主要长度为7至9个核苷酸。聚(dIT)是迄今为止发现的最具活性的模板。该活性似乎具有“宽松”的底物/模板互补性要求,类似于先前描述的哺乳动物引发酶的要求;仅含rATP的聚(dIT)模板会导致合成与同时存在rATP和rCTP时合成的寡聚(rAC)大小相同的寡聚(rA)。当向反应中添加dNTPs时,DNA通过作为引物的寡核糖核苷酸的延伸而合成。DNA产物呈现出相对离散的大小,相差约8个核苷酸,大部分产物在24和32个核苷酸左右。除了产物大小相对离散外,在聚(dIT)模板上利用内源性合成的寡核糖核苷酸引物的DNA聚合酶活性在对阿非科林的抗性和对dNTP的低Km方面与聚合酶α不同。

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