Human DINB1-encoded DNA polymerase κ is a promiscuous extender of mispaired primer termini

被引:139
作者
Washington, MT [1 ]
Johnson, RE [1 ]
Prakash, L [1 ]
Prakash, S [1 ]
机构
[1] Univ Texas, Med Branch, Sealy Ctr Mol Sci, Galveston, TX 77555 USA
关键词
D O I
10.1073/pnas.032594399
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
Both in yeast and humans, DNA polymerase (Pol) eta functions in the error-free replication of UV-damaged DNA, and Poleta has the unique ability to efficiently replicate through a cis-syn thymine-thymine (T-T) dimer by inserting two As opposite the two Ts of the dimer. Although human DINB1-encoded Polkappa belongs to the same protein family as Poleta, Polkappa shows no ability to bypass this DNA lesion and its biological function has remained unclear. Here, we examine Polkappa for its ability to extend from primer-terminal mispairs opposite nondamaged and damaged DNA templates. We find that Polkappa is a promiscuous extender of primer-terminal mispairs opposite nondamaged DNA templates, and interestingly, it is also very efficient at extending from a G opposite the 3'T of a T-T dimer. These observations provide biochemical evidence for a role Of Polkappa in the extension of mismatched base pairs during normal DNA replication, and in addition, they implicate Polkappa in the mutagenic bypass of T-T dimers. In its proficient mismatch extension ability, Polkappa is more similar to the unrelated DNA polymerase than it is to the phylogenetically related Poleta or Poliota. Thus, in humans, Polkappa would compete with Polzeta for the extension of mismatched base pairs on damaged and undamaged DNAs.
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页码:1910 / 1914
页数:5
相关论文
共 29 条
[21]  
Tissier A, 2000, GENE DEV, V14, P1642
[22]   Structure of the catalytic core of S-cerevisiae DNA polymerase η:: Implications for translesion DNA synthesis [J].
Trincao, J ;
Johnson, RE ;
Escalante, CR ;
Prakash, S ;
Prakash, L ;
Aggarwal, AK .
MOLECULAR CELL, 2001, 8 (02) :417-426
[23]   Mismatch extension ability of yeast and human DNA polymerase η [J].
Washington, MT ;
Johnson, RE ;
Prakash, S ;
Prakashs, L .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (03) :2263-2266
[24]   Accuracy of thymine-thymine dimer bypass by Saccharomyces cerevisiae DNA polymerase η [J].
Washington, MT ;
Johnson, RE ;
Prakash, S ;
Prakash, L .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (07) :3094-3099
[25]   Accuracy of lesion bypass by yeast and human DNA polymerase η [J].
Washington, MT ;
Johnson, RE ;
Prakash, L ;
Prakash, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (15) :8355-8360
[26]   Fidelity and processivity of Saccharomyces cerevisiae DNA polymerase η [J].
Washington, MT ;
Johnson, RE ;
Prakash, S ;
Prakash, L .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (52) :36835-36838
[27]   AN INDUCED-FIT KINETIC MECHANISM FOR DNA-REPLICATION FIDELITY - DIRECT MEASUREMENT BY SINGLE-TURNOVER KINETICS [J].
WONG, I ;
PATEL, SS ;
JOHNSON, KA .
BIOCHEMISTRY, 1991, 30 (02) :526-537
[28]   Requirement of DNA polymerase η for error-free bypass of UV-induced CC and TC photoproducts [J].
Yu, SL ;
Johnson, RE ;
Prakash, S ;
Prakash, L .
MOLECULAR AND CELLULAR BIOLOGY, 2001, 21 (01) :185-188
[29]   Crystal structure of a DinB lesion bypass DNA polymerase catalytic fragment reveals a classic polymerase catalytic domain [J].
Zhou, BL ;
Pata, JD ;
Steitz, TA .
MOLECULAR CELL, 2001, 8 (02) :427-437