Replication by human DNA polymerase-ι occurs by Hoogsteen base-pairing

被引:265
作者
Nair, DT
Johnson, RE
Prakash, S
Prakash, L
Aggarwal, AK
机构
[1] Mt Sinai Sch Med, Dept Physiol & Biophys, Struct Biol Program, New York, NY 10029 USA
[2] Univ Texas, Med Branch, Sealy Ctr Mol Sci, Galveston, TX 77755 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1038/nature02692
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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. hPoli 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(1-5). 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.
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页码:377 / 380
页数:4
相关论文
共 28 条
[1]  
Brunger AT, 1998, ACTA CRYSTALLOGR D, V54, P905, DOI 10.1107/s0907444998003254
[2]   An error-prone family Y DNA polymerase (DinB homolog from Sulfolobus solfataricus) uses a 'steric gate' residue for discrimination against ribonucleotides [J].
DeLucia, AM ;
Grindley, NDF ;
Joyce, CM .
NUCLEIC ACIDS RESEARCH, 2003, 31 (14) :4129-4137
[3]   Crystal structure of a bacteriophage T7 DNA replication complex at 2.2 Å resolution [J].
Doublié, S ;
Tabor, S ;
Long, AM ;
Richardson, CC ;
Ellenberger, T .
NATURE, 1998, 391 (6664) :251-258
[4]   Induction of somatic hypermutation in immunoglobulin genes is dependent on DNA polymerase iota [J].
Faili, A ;
Aoufouchi, S ;
Flatter, E ;
Guéranger, Q ;
Reynaud, CA ;
Weill, JC .
NATURE, 2002, 419 (6910) :944-947
[5]   Targeting of human DNA polymerase ι to the replication machinery via interaction with PCNA [J].
Haracska, L ;
Johnson, RE ;
Unk, I ;
Phillips, BB ;
Hurwitz, J ;
Prakash, L ;
Prakash, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (25) :14256-14261
[6]   Eukaryotic polymerases ι and ζ act sequentially to bypass DNA lesions [J].
Johnson, RE ;
Washington, MT ;
Haracska, L ;
Prakash, S ;
Prakash, L .
NATURE, 2000, 406 (6799) :1015-1019
[7]   Efficient bypass of a thymine-thymine dimer by yeast DNA polymerase, Polη [J].
Johnson, RE ;
Prakash, S ;
Prakash, L .
SCIENCE, 1999, 283 (5404) :1001-1004
[8]   hRAD30 mutations in the variant form of xeroderma pigmentosum [J].
Johnson, RE ;
Kondratick, CM ;
Prakash, S ;
Prakash, L .
SCIENCE, 1999, 285 (5425) :263-265
[9]   Fidelity of human DNA polymerase η [J].
Johnson, RE ;
Washington, MT ;
Prakash, S ;
Prakash, L .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (11) :7447-7450
[10]   Deoxynucleotide triphosphate binding mode conserved in Y family DNA polymerases [J].
Johnson, RE ;
Trincao, J ;
Aggarwal, AK ;
Prakash, S ;
Prakash, L .
MOLECULAR AND CELLULAR BIOLOGY, 2003, 23 (08) :3008-3012