The effect of a G:T mispair on the dynamics of DNA.

Distortions in the DNA sequence such as damages or mispairs are specifically recognized and processed by DNA repair enzymes. A particular challenge for the enzymatic specificity is the recognition of a wrongly-placed native nucleotide such as thymine in T:G mispairs. An important step of substrate b...

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Main Authors: Petra Imhof, Mai Zahran
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3546078?pdf=render
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spelling doaj-fcd3cd5f9e494cb09568c1cae331a57b2020-11-25T02:09:18ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0181e5330510.1371/journal.pone.0053305The effect of a G:T mispair on the dynamics of DNA.Petra ImhofMai ZahranDistortions in the DNA sequence such as damages or mispairs are specifically recognized and processed by DNA repair enzymes. A particular challenge for the enzymatic specificity is the recognition of a wrongly-placed native nucleotide such as thymine in T:G mispairs. An important step of substrate binding which is observed in many repair proteins is the flipping of the target base out of the DNA helix into the enzyme's active site. In this work we investigate how much the intrinsic dynamics of mispaired DNA is changed compared to canonical DNA. Our molecular dynamics simulations of DNA with and without T:G mispairs show significant differences in the conformation of paired and mispaired DNA. The wobble pair T:G shows local distortions such as twist, shear and stretch which deviate from canonical B form values. Moreover, the T:G mispair is found to be kinetically less stable, exhibiting two states with respect to base opening: a closed state comparable to the canonical base pairs, and a more open state, indicating a proneness for base flip. In addition, we observe that the thymine base in a T:G mispair is significantly more probable to be flipped than thymine in a T:A pair or cytosine in a C:G pair. Such local deformations and in particular the existence of a second, more-open state can be speculated to help the target-site recognition by repair enzymes.http://europepmc.org/articles/PMC3546078?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Petra Imhof
Mai Zahran
spellingShingle Petra Imhof
Mai Zahran
The effect of a G:T mispair on the dynamics of DNA.
PLoS ONE
author_facet Petra Imhof
Mai Zahran
author_sort Petra Imhof
title The effect of a G:T mispair on the dynamics of DNA.
title_short The effect of a G:T mispair on the dynamics of DNA.
title_full The effect of a G:T mispair on the dynamics of DNA.
title_fullStr The effect of a G:T mispair on the dynamics of DNA.
title_full_unstemmed The effect of a G:T mispair on the dynamics of DNA.
title_sort effect of a g:t mispair on the dynamics of dna.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2013-01-01
description Distortions in the DNA sequence such as damages or mispairs are specifically recognized and processed by DNA repair enzymes. A particular challenge for the enzymatic specificity is the recognition of a wrongly-placed native nucleotide such as thymine in T:G mispairs. An important step of substrate binding which is observed in many repair proteins is the flipping of the target base out of the DNA helix into the enzyme's active site. In this work we investigate how much the intrinsic dynamics of mispaired DNA is changed compared to canonical DNA. Our molecular dynamics simulations of DNA with and without T:G mispairs show significant differences in the conformation of paired and mispaired DNA. The wobble pair T:G shows local distortions such as twist, shear and stretch which deviate from canonical B form values. Moreover, the T:G mispair is found to be kinetically less stable, exhibiting two states with respect to base opening: a closed state comparable to the canonical base pairs, and a more open state, indicating a proneness for base flip. In addition, we observe that the thymine base in a T:G mispair is significantly more probable to be flipped than thymine in a T:A pair or cytosine in a C:G pair. Such local deformations and in particular the existence of a second, more-open state can be speculated to help the target-site recognition by repair enzymes.
url http://europepmc.org/articles/PMC3546078?pdf=render
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