Repair of genomic double-strand breaks in somatic plant cells by one-sided invasion of homologous sequences

被引:97
作者
Puchta, H [1 ]
机构
[1] Inst Pflanzengenet & Kultur Pflanzenforsch, D-06466 Gatersleben, Germany
关键词
D O I
10.1046/j.1365-313X.1998.00035.x
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Double-strand breaks (DSB) strongly enhance homologous recombination in the genome of somatic plant cells. To characterize the mechanism of homologous DSB repair in detail, Agrobacterium-mediated targeting experiments were performed in tobacco, with repair constructs being homologous to either one or both ends of a transiently induced DSB. The recombination frequencies obtained were at least two orders of magnitude higher than without DSB induction and differed between the two T-DNA by only one-third. Thus, occurrence of homologies at both ends of the break is no prerequisite for recombination. The results demonstrate that most, if not all, reactions are initiated by one-sided invasion of a homologous sequence. This indicates that the classical double-strand break repair (DSBR) model originally proposed for meiotic recombination might be less appropriate for the description of homologous DSB repair in somatic plant cells than an integrative model based on a combination of the synthesis-dependent strand annealing (SDSA) model and of a modified version of the one-sided invasion (OSI) model of recombination. Direct consequences of this finding for the performance of gene targeting experiments, as well as possible implications for the stability of highly repetitive plant genomes, are discussed.
引用
收藏
页码:331 / 339
页数:9
相关论文
共 47 条
[1]  
ATHMA P, 1991, GENETICS, V128, P163
[2]   ONE-SIDED INVASION EVENTS IN HOMOLOGOUS RECOMBINATION AT DOUBLE-STRAND BREAKS [J].
BELMAAZA, A ;
CHARTRAND, P .
MUTATION RESEARCH, 1994, 314 (03) :199-208
[3]   BINARY AGROBACTERIUM VECTORS FOR PLANT TRANSFORMATION [J].
BEVAN, M .
NUCLEIC ACIDS RESEARCH, 1984, 12 (22) :8711-8721
[4]   SINGLE-STRANDED-DNA AS A RECOMBINATION SUBSTRATE IN PLANTS AS ASSESSED BY STABLE AND TRANSIENT RECOMBINATION ASSAYS [J].
BILANG, R ;
PETERHANS, A ;
BOGUCKI, A ;
PASZKOWSKI, J .
MOLECULAR AND CELLULAR BIOLOGY, 1992, 12 (01) :329-336
[5]   TRANSKINGDOM T-DNA TRANSFER FROM AGROBACTERIUM-TUMEFACIENS TO SACCHAROMYCES-CEREVISIAE [J].
BUNDOCK, P ;
DENDULKRAS, A ;
BEIJERSBERGEN, A ;
HOOYKAAS, PJJ .
EMBO JOURNAL, 1995, 14 (13) :3206-3214
[6]   Enhancement of somatic intrachromosomal homologous recombination in Arabidopsis by the HO endonuclease [J].
Chiurazzi, M ;
Ray, A ;
Viret, JF ;
Perera, R ;
Wang, XH ;
Lloyd, AM ;
Signer, ER .
PLANT CELL, 1996, 8 (11) :2057-2066
[7]  
CHOULIKA A, 1995, MOL CELL BIOL, V15, P1968
[8]  
DeNeve M, 1997, PLANT J, V11, P15, DOI 10.1046/j.1365-313X.1997.11010015.x
[9]   Recombinational repair of gaps in DNA is asymmetric in Ustilago maydis and can be explained by a migrating D-loop model [J].
Ferguson, DO ;
Holloman, WK .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (11) :5419-5424
[10]   REMOVAL OF NONHOMOLOGOUS DNA ENDS IN DOUBLE-STRAND BREAK RECOMBINATION - THE ROLE OF THE YEAST ULTRAVIOLET REPAIR GENE RAD1 [J].
FISHMANLOBELL, J ;
HABER, JE .
SCIENCE, 1992, 258 (5081) :480-484