首页> 美国卫生研究院文献>Nucleic Acids Research >Selection of template initiation sites and the lengths of RNA primers synthesized by DNA primase are strongly affected by its organization in a multiprotein DNA polymerase alpha complex.
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Selection of template initiation sites and the lengths of RNA primers synthesized by DNA primase are strongly affected by its organization in a multiprotein DNA polymerase alpha complex.

机译:模板起始位点的选择和DNA引发酶合成的RNA引物的长度受其在多蛋白DNA聚合酶α复合物中的组织的强烈影响。

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摘要

Synthesis of (p)ppRNA-DNA chains by purified HeLa cell DNA primase-DNA polymerase alpha (pol alpha-primase) was compared with those synthesized by a multiprotein form of DNA polymerase alpha (pol alpha 2) using unique single-stranded DNA templates containing the origin of replication for simian virus 40 (SV40) DNA. The nucleotide locations of 33 initiation sites were identified by mapping G*pppN-RNA-DNA chains and identifying their 5'-terminal ribonucleotide. Pol alpha 2 strongly preferred initiation sites that began with ATP rather than GTP, thus frequently preferring different initiation sites than pol alpha-primase, depending on the template examined. The initiation sites selected in vitro, however, did not correspond to the sites used during SV40 DNA replication in vivo. Pol alpha 2 had the greatest effect on RNA primer size, typically synthesizing primers 1-5 nucleotides long, while pol alpha-primase synthesized primers 6-8 nucleotides long. These differences were observed even at individual initiation sites. Thus, the multiprotein form of DNA primase-DNA polymerase alpha affects selection of initiation sites, the frequency at which the sites are chosen, and length of RNA primers.
机译:使用独特的单链DNA模板,将通过纯化的HeLa细胞DNA primase-DNA聚合酶α(pol alpha-primase)合成的(p)ppRNA-DNA链与通过DNA聚合酶alpha(pol alpha 2)的多蛋白形式合成的链进行比较。包含猿猴病毒40(SV40)DNA的复制起点。通过定位G * pppN-RNA-DNA链并鉴定其5'-末端核糖核苷酸来鉴定33个起始位点的核苷酸位置。 Polα2强烈优选以ATP而不是GTP开头的起始位点,因此,取决于所检查的模板,与pol alpha引物酶相比,它们通常更喜欢不同的起始位点。然而,体外选择的起始位点与体内SV40 DNA复制过程中使用的位点不对应。 Pol alpha 2对RNA引物大小的影响最大,通常合成长度为1-5个核苷酸的引物,而pol alpha-primase合成的长度为6-8个核苷酸的引物。即使在各个起始位点也观察到这些差异。因此,DNA primase-DNA polymerase alpha的多蛋白形式会影响起始位点的选择,位点的选择频率以及RNA引物的长度。

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