Human DNA polymerase ι incorporates dCTP opposite template G via a G.C plus hoogsteen base pair

被引:112
作者
Nair, DT
Johnson, RE
Prakash, L
Prakash, S
Aggarwal, AK
机构
[1] CUNY Mt Sinai Sch Med, Struct Biol Program, Dept Physiol & Biophys, New York, NY 10029 USA
[2] Univ Texas, Sealy Ctr Mol Sci, Med Branch 6014, Galveston, TX 77755 USA
关键词
D O I
10.1016/j.str.2005.08.010
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Human DNA polymerase iota (hPol iota), a member of the Y family of DNA polymerases, differs in remarkable ways from other DNA polymerases, incorporating correct nucleotides opposite template purines with a much higher efficiency and fidelity than opposite template pyrimidines. We present here the crystal structure of hPol iota bound to template G and incoming dCTP which reveals a G.C+ Hoogsteen base pair in a DNA polymerase active site. We show that the hPol iota, active site has evolved to favor Hoogsteen base pairing, wherein the template sugar is fixed in a cavity that reduces the C1'-C1' distance across the nascent base pair from similar to 10.5 angstrom in other DNA polymerases to 8.6 angstrom in hPol iota. The rotation of G from anti to syn is then largely in response to this curtailed C1'-C1' distance. A G.C+ Hoogsteen base pair suggests a specific mechanism for hPoli's ability to bypass N2-adducted guanines that obstruct replication.
引用
收藏
页码:1569 / 1577
页数:9
相关论文
共 44 条
[1]   The contribution of cytosine protonation to the stability of parallel DNA triple helices [J].
Asensio, JL ;
Lane, AN ;
Dhesi, J ;
Bergqvist, S ;
Brown, T .
JOURNAL OF MOLECULAR BIOLOGY, 1998, 275 (05) :811-822
[2]   A NUCLEIC-ACID TRIPLE-HELIX FORMED BY A PEPTIDE NUCLEIC-ACID DNA COMPLEX [J].
BETTS, L ;
JOSEY, JA ;
VEAL, JM ;
JORDAN, SR .
SCIENCE, 1995, 270 (5243) :1838-1841
[3]   Structural basis for the dual coding potential of 8-oxoguanosine by a high-fidelity DNA polymerase [J].
Brieba, LG ;
Eichman, BF ;
Kokoska, RJ ;
Doublié, S ;
Kunkel, TA ;
Ellenberger, T .
EMBO JOURNAL, 2004, 23 (17) :3452-3461
[4]  
Brunger AT, 1998, ACTA CRYSTALLOGR D, V54, P905, DOI 10.1107/s0907444998003254
[5]  
DeLano W., PYMOL MOL GRAPHICS S
[6]   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
[7]   Knowledge-based protein secondary structure assignment [J].
Frishman, D ;
Argos, P .
PROTEINS-STRUCTURE FUNCTION AND GENETICS, 1995, 23 (04) :566-579
[8]   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
[9]   Error-prone replication of oxidatively damaged DNA by a high-fidelity DNA polymerase [J].
Hsu, GW ;
Ober, M ;
Carell, T ;
Beese, LS .
NATURE, 2004, 431 (7005) :217-221
[10]   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