Repair bias of large loop mismatches during recombination in mammalian cells depends on loop length and structure

被引:20
作者
Bill, CA
Taghian, DG
Duran, WA
Nickoloff, JA [1 ]
机构
[1] Univ New Mexico, Sch Med, Dept Mol Genet & Microbiol, Albuquerque, NM 87131 USA
[2] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Dept Radiat Oncol, Boston, MA 02129 USA
来源
MUTATION RESEARCH-DNA REPAIR | 2001年 / 485卷 / 03期
关键词
homologous recombination; heteroduplex DNA; palindromes; MSH2; genome stability; DNA polymerase slippage;
D O I
10.1016/S0921-8777(01)00065-9
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Repair of loop mismatches was investigated in wild-type and mismatch binding-defective Chinese hamster ovary (CHO) cells. Loop mismatches were formed in vivo during extrachromosomal recombination between heteroallelic plasmid substrates. Recombination was expected to occur primarily by single-strand annealing (SSA), yielding 12- or 26-base nonpalindromic loop mismatches, and 12-, 26-, or 40-base palindromic loop mismatches. Nonpalindromic loops were repaired efficiently and with bias toward loop loss. In contrast, the 12-base palindromic loop was repaired with bias toward loop retention, indicating that repair bias depends on loop structure. Among the palindromic loops, repair bias was dependent on loop length, with bias shifting from loop retention to loop loss with increasing loop size. For both palindromic and nonpalindromic loops, repair efficiencies and biases were independent of the general (MSH/MLH) mismatch repair pathway. These results are discussed with respect to the maintenance of large nonpalindromic insertions, and of small and large palindromes, in eukaryotic genomes. (C) 2001 Published by Elsevier Science B.V.
引用
收藏
页码:255 / 265
页数:11
相关论文
共 86 条
[21]  
Eshleman James R., 1995, Current Opinion in Oncology, V7, P83
[22]  
FANG WH, 1993, J BIOL CHEM, V268, P11838
[23]   THE HUMAN MUTATOR GENE HOMOLOG MSH2 AND ITS ASSOCIATION WITH HEREDITARY NONPOLYPOSIS COLON-CANCER [J].
FISHEL, R ;
LESCOE, MK ;
RAO, MRS ;
COPELAND, NG ;
JENKINS, NA ;
GARBER, J ;
KANE, M ;
KOLODNER, R .
CELL, 1993, 75 (05) :1027-1038
[24]   MutS homologs in mammalian cells [J].
Fishel, R ;
Wilson, T .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 1997, 7 (01) :105-113
[25]   A TRANSCRIPTIONALLY ACTIVE DNA-BINDING SITE FOR HUMAN P53 PROTEIN COMPLEXES [J].
FUNK, WD ;
PAK, DT ;
KARAS, RH ;
WRIGHT, WE ;
SHAY, JW .
MOLECULAR AND CELLULAR BIOLOGY, 1992, 12 (06) :2866-2871
[26]   Isolation of MutSβ from human cells and comparison of the mismatch repair specificities of MutSβ and MutSα [J].
Genschel, J ;
Littman, SJ ;
Drummond, JT ;
Modrich, P .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (31) :19895-19901
[27]   Discrete in vivo roles for the MutL homologs Mlh2p and Mlh3p in the removal of frameshift intermediates in budding yeast [J].
Harfe, BD ;
Minesinger, BK ;
Jinks-Robertson, S .
CURRENT BIOLOGY, 2000, 10 (03) :145-148
[28]  
Harfe BD, 1999, MOL CELL BIOL, V19, P4766
[29]  
HAUN RS, 1993, J BIOL CHEM, V268, P8793
[30]   THE STABILIZATION OF REPETITIVE TRACTS OF DNA BY VARIANT REPEATS REQUIRES A FUNCTIONAL DNA MISMATCH REPAIR SYSTEM [J].
HEALE, SM ;
PETES, TD .
CELL, 1995, 83 (04) :539-545