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古菌引物酶充当纳米卡尺以定义引物长度。

An archaeal primase functions as a nanoscale caliper to define primer length.

机构信息

Molecular and Cellular Biochemistry Department, Indiana University, Bloomington, IN 47405.

Department of Biochemistry, University of Cambridge, Cambridge CB2 1QW, United Kingdom.

出版信息

Proc Natl Acad Sci U S A. 2018 Jun 26;115(26):6697-6702. doi: 10.1073/pnas.1806351115. Epub 2018 Jun 11.

Abstract

The cellular replicative DNA polymerases cannot initiate DNA synthesis without a priming 3' OH. During DNA replication, this is supplied in the context of a short RNA primer molecule synthesized by DNA primase. The primase of archaea and eukaryotes, despite having varying subunit compositions, share sequence and structural homology. Intriguingly, archaeal primase has been demonstrated to possess the ability to synthesize DNA de novo, a property shared with the eukaryotic PrimPol enzymes. The dual RNA and DNA synthetic capabilities of the archaeal DNA primase have led to the proposal that there may be a sequential hand-off between these synthetic modes of primase. In the current work, we dissect the functional interplay between DNA and RNA synthetic modes of primase. In addition, we determine the key determinants that govern primer length definition by the archaeal primase. Our results indicate a primer measuring system that functions akin to a caliper.

摘要

细胞复制 DNA 聚合酶在没有引发 3'OH 的情况下无法启动 DNA 合成。在 DNA 复制过程中,这是由 DNA 引发酶合成的短 RNA 引物分子提供的。古菌和真核生物的引发酶尽管亚基组成不同,但具有序列和结构同源性。有趣的是,已经证明古菌的引发酶具有从头合成 DNA 的能力,这一特性与真核 PrimPol 酶共享。古菌 DNA 引发酶的双重 RNA 和 DNA 合成能力导致人们提出,在这些引发酶的合成模式之间可能存在顺序交接。在目前的工作中,我们剖析了引发酶的 DNA 和 RNA 合成模式之间的功能相互作用。此外,我们确定了控制古菌引发酶定义引物长度的关键决定因素。我们的结果表明,引物测量系统的功能类似于卡尺。

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