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Polymerization behavior of Klenow fragment and Taq DNA polymerase in short primer extension reactions.

Guojie Zhao, +1 more
- 01 Oct 2010 - 
- Vol. 42, Iss: 10, pp 722-728
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TLDR
It was found that the longer the primer, the more efficient is the primer extension, and these polymerization behavior of short primers lay foundation about DNA polymerization mechanism and development of novel nucleic acid detection assays.
Abstract
DNA polymerases amplify DNA fragments through primer extension reactions. However, polymerization behavior of short primers in the primer extension process has not been systematically explored. In this study, we examined the minimal primer length required for primer extension, and the effect of primer length, mismatches and other conditions on DNA polymerization using a non-radioactive method. Under the condition we conducted, the shortest primers polymerized by Klenow fragment (KF) and Taq DNA polymerase in our experiments were respectively heptamer and octamer. The extension efficiency was also affected by the up-stream overhanging structure of the primer-template complex. We hypothesized a simple model to interpret these observations based on the polymerase structures. Furthermore, it was found that the longer the primer, the more efficient is the primer extension. These polymerization behavior of short primers lay foundation about DNA polymerization mechanism and development of novel nucleic acid detection assays.

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References
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Journal Article

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Effects of primer-template mismatches on the polymerase chain reaction: Human immunodeficiency virus type 1 model studies

TL;DR: The effects of various primer-template mismatches on DNA amplification of an HIV-1 gag region by the polymerase chain reaction (PCR) were investigated, although the G:G mismatches appeared to be more sensitive to sequence context and dNTP concentrations than other mismatches.
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DNA Polymerases: Structural Diversity and Common Mechanisms

TL;DR: Of particular interest are the role of editing in the fidelity of copying, the common enzymatic mechanism of polymerases, and the manners in which different domain structures function in the polymerase reaction in analogous ways.
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Structures of ternary complexes of rat DNA polymerase beta, a DNA template-primer, and ddCTP.

TL;DR: Two ternary complexes of rat DNA polymerase beta, a DNA template-primer, and dideoxycytidine triphosphate have been determined at 2.9 A and 3.6 A resolution, suggesting that the polymerase-DNA-ddCTP interactions are not affected by crystal packing forces.
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