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微基因聚合反应中重复传播的动力学

Kinetics of repeat propagation in the microgene polymerization reaction.

作者信息

Itsko Mark, Rabinovitch Avinoam, Zaritsky Arieh

机构信息

Department of Life Sciences, Ben-Gurion University of the Negev, Be'er-Sheva 84105, Israel.

出版信息

Biophys J. 2009 Mar 4;96(5):1866-74. doi: 10.1016/j.bpj.2008.10.061.

DOI:10.1016/j.bpj.2008.10.061
PMID:19254545
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2717307/
Abstract

Repetitive DNA is a periodic copolymer with the intrinsic property of exponential propagation to longer repeats. Microgene polymerization reaction (MPR) is a model system in which a short nonrepetitive homo-duplex DNA evolves to multiple repetitive products during heat-cool cycles. The mechanism underlying this process involves staggered annealing of complementary DNA strands of variable lengths and polymerase-mediated filling-in of the generated overhangs. MPR is considered here as a process sharing common features with two polymerization types, chain-growth and step-growth, and significant distinctions from both types were highlighted. The involved reaction stages were formulated and a kinetic model was derived and tested experimentally. The model can quantitatively explain MPR propagation and be used as a good approximation for this phenomenon.

摘要

重复DNA是一种具有指数级传播至更长重复序列内在特性的周期性共聚物。微基因聚合反应(MPR)是一种模型系统,在该系统中,短的非重复同源双链DNA在热循环冷却过程中演变成多个重复产物。这一过程的潜在机制涉及不同长度互补DNA链的交错退火以及聚合酶介导的对产生的突出端的填补。本文将MPR视为一个与链增长和逐步增长这两种聚合类型具有共同特征的过程,并突出了与这两种类型的显著区别。阐述了所涉及的反应阶段,推导了动力学模型并进行了实验测试。该模型可以定量解释MPR的传播,并可作为对这一现象的良好近似。

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引用本文的文献

1
Kinetics and thermodynamics of the microgene polymerization reaction.微基因聚合反应的动力学与热力学
Biophys J. 2009 Mar 4;96(5):1673-4. doi: 10.1016/j.bpj.2008.11.010.

本文引用的文献

1
Thermodynamics of unstable DNA structures from the kinetics of the microgene PCR.基于微基因聚合酶链反应动力学的不稳定DNA结构的热力学
J Phys Chem B. 2008 Oct 16;112(41):13149-56. doi: 10.1021/jp8045142. Epub 2008 Sep 17.
2
Initiation of the microgene polymerization reaction with non-repetitive homo-duplexes.使用非重复同源双链体引发微基因聚合反应。
Biochem Biophys Res Commun. 2008 Apr 11;368(3):606-13. doi: 10.1016/j.bbrc.2008.01.108. Epub 2008 Feb 1.
3
A synthesis approach to understanding repeated peptides conserved in mineralization proteins.一种理解矿化蛋白中保守重复肽段的综合方法。
Biomacromolecules. 2007 Sep;8(9):2659-64. doi: 10.1021/bm700652b. Epub 2007 Aug 1.
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Expandable DNA repeats and human disease.可扩展的DNA重复序列与人类疾病
Nature. 2007 Jun 21;447(7147):932-40. doi: 10.1038/nature05977.
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Exposing cryptic antibacterial activity in Cyt1Ca from Bacillus thuringiensis israelensis by genetic manipulations.通过基因操作揭示苏云金芽孢杆菌以色列亚种Cyt1Ca中的隐秘抗菌活性。
FEBS Lett. 2007 May 1;581(9):1775-82. doi: 10.1016/j.febslet.2007.03.064. Epub 2007 Apr 2.
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Motif programming: a microgene-based method for creating synthetic proteins containing multiple functional motifs.基序编程:一种基于微基因的方法,用于创建包含多个功能基序的合成蛋白质。
Nucleic Acids Res. 2007;35(6):e38. doi: 10.1093/nar/gkm017. Epub 2007 Feb 7.
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Very efficient template/primer-independent DNA synthesis by thermophilic DNA polymerase in the presence of a thermophilic restriction endonuclease.嗜热DNA聚合酶在嗜热限制性内切核酸酶存在下进行的高效模板/引物非依赖性DNA合成。
Biochemistry. 2004 Oct 26;43(42):13459-66. doi: 10.1021/bi0489614.
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Molecular structure of nucleic acids; a structure for deoxyribose nucleic acid.核酸的分子结构;脱氧核糖核酸的一种结构。
Nature. 1953 Apr 25;171(4356):737-8. doi: 10.1038/171737a0.
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On the role of periodism in the origin of proteins.论周期性在蛋白质起源中的作用。
J Mol Biol. 2002 Jul 19;320(4):833-40. doi: 10.1016/s0022-2836(02)00567-3.
10
Mechanism of in vitro expansion of long DNA repeats: effect of temperature, repeat length, repeat sequence, and DNA polymerases.长DNA重复序列的体外扩增机制:温度、重复长度、重复序列及DNA聚合酶的影响
Biochemistry. 2002 Jan 22;41(3):854-60. doi: 10.1021/bi0110950.