Home LiteratureArticle Details
PMID: 15254543 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Replication by human DNA polymerase-iota occurs by Hoogsteen base-pairing.

Nature ·Vol. 430 ·No. 6997 ·2004-07-15 ·Pages 377-80

Nair DT, Johnson RE, Prakash S, Prakash L, Aggarwal AK

Abstract

Almost all DNA polymerases show a strong preference for incorporating the nucleotide that forms the correct Watson-Crick base pair with the template base. In addition, the catalytic efficiencies with which any given polymerase forms the four possible correct base pairs are roughly the same. Human DNA polymerase-iota (hPoliota), a member of the Y family of DNA polymerases, is an exception to these rules. hPoliota incorporates the correct nucleotide opposite a template adenine with a several hundred to several thousand fold greater efficiency than it incorporates the correct nucleotide opposite a template thymine, whereas its efficiency for correct nucleotide incorporation opposite a template guanine or cytosine is intermediate between these two extremes. Here we present the crystal structure of hPoliota bound to a template primer and an incoming nucleotide. The structure reveals a polymerase that is 'specialized' for Hoogsteen base-pairing, whereby the templating base is driven to the syn conformation. Hoogsteen base-pairing offers a basis for the varied efficiencies and fidelities of hPoliota opposite different template bases, and it provides an elegant mechanism for promoting replication through minor-groove purine adducts that interfere with replication.

MeSH Terms
Base Pairing Binding Sites Crystallization Crystallography, X-Ray DNA/biosynthesis,chemistry,genetics DNA Replication DNA-Directed DNA Polymerase/chemistry,metabolism Humans Models, Molecular Protein Binding Protein Conformation Structure-Activity Relationship Templates, Genetic
Chemicals
DNA DNA polymerase iota DNA-Directed DNA Polymerase
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Nair Deepak T
Structural Biology Program, Department of Physiology and Biophysics, Mount Sinai School of Medicine, Box 1677, 1425 Madison Avenue, New York, New York 10029, USA.
Johnson Robert E
Prakash Satya
Prakash Louise
Aggarwal Aneel K
Article Info
Journal
Nature
Abbr.
Nature
ISSN
1476-4687
Published
2004-07-15
Pages
377-80
Language
English
Region
England
NLM ID
0410462
Subset
IM
Databases
PDB
Corrections
CommentIn
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