Title of article
Discrimination against the Cytosine Analog tC by Escherichia coli DNA Polymerase IV DinB
Author/Authors
Jason M. Walsh، نويسنده , , Imenne Bouamaied، نويسنده , , Tom Brown، نويسنده , , L. Marcus Wilhelmsson، نويسنده , , Penny J. Beuning، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2011
Pages
12
From page
89
To page
100
Abstract
The cytosine analog 1,3-diaza-2-oxophenothiazine (tC) is a fluorescent nucleotide that forms Watson–Crick base pairs with dG. The Klenow fragment of DNA polymerase I (an A-family polymerase) can efficiently bypass tC on the template strand and incorporate deoxyribose-triphosphate-tC into the growing primer terminus. Y-family DNA polymerases are known for their ability to accommodate bulky lesions and modified bases and to replicate beyond such nonstandard DNA structures in a process known as translesion synthesis. We probed the ability of the Escherichia coli Y-family DNA polymerase DinB (Pol IV) to copy DNA containing tC and to incorporate tC into a growing DNA strand. DinB selectively adds dGTP across from tC in template DNA but cannot extend beyond the newly formed G:tC base pair. However, we find that DinB incorporates the tC deoxyribonucleotide triphosphate opposite template G and extends from tC. Therefore, DinB displays asymmetry in terms of its ability to discriminate against the modification of the DNA template compared to the incoming nucleotide. In addition, our finding that DinB (a lesion-bypass DNA polymerase) specifically discriminates against tC in the template strand may suggest that DinB discriminates against template modifications in the major groove of DNA.
Keywords
primer extension , tryptophan fluorescence binding assay , major groove , translesion synthesis
Journal title
Journal of Molecular Biology
Serial Year
2011
Journal title
Journal of Molecular Biology
Record number
1253766
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