Capture of extranuclear DNA at fission yeast double-strand breaks

被引:23
作者
Decottignies, A [1 ]
机构
[1] Catholic Univ Louvain, Christian de Duve Inst Cellular Pathol, B-1200 Brussels, Belgium
关键词
D O I
10.1534/genetics.105.046144
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Proper repair of DNA double-strand breaks (DSBs) is necessary for the maintenance of genomic integrity. Here, a new simple assay was used to Study extrachromosomal DSB repair in Schizosaccharomyces pombe. Strikingly, DSB repair was associated with the capture of fission yeast mitochondrial DNA (mtDNA) at high frequency. Capture of mtDNA fragments required the Lig4p/Pku70p nonhomologous endjoining (NHEJ) machinery and its frequency was highly increased in fission yeast cells grown to stationary phase. The fission yeast Well complex Rad32p/Rad50p/Nbs1p was also required for efficient capture of mtDNA at DSBs, supporting a role for the complex in promoting intermolecular ligation. Competition assays further revealed that microsatellite DNA from higher eukaryotes was preferentially captured at yeast DSBs. Finally, cotransformation experiments indicated that, in NHEJ-deficient cells, capture of extranuclear DNA at DSBs was observed if hortiologies-as short as 8 bp-were present between DNA substrate and DSB ends. Hence, whether driven by NHEJ, microhomology-mediated endjoining, or homologous recombination, DNA capture associated with DSB repair is a mutagenic process threatening genomic stability.
引用
收藏
页码:1535 / 1548
页数:14
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共 70 条
[11]   Promotion of Dnl4-catalyzed DNA end-joining by the Rad50/Mre11/Xrs2 and Hdfl/Hdf2 complexes [J].
Chen, L ;
Trujillo, K ;
Ramos, W ;
Sung, P ;
Tomkinson, AE .
MOLECULAR CELL, 2001, 8 (05) :1105-1115
[12]   The Mre11 complex: At the crossroads of DNA repair and checkpoint signalling [J].
D'Amours, D ;
Jackson, SP .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2002, 3 (05) :317-327
[13]   Large-scale screening of intracellular protein localization in living fission yeast cells by the use of a GFP-fusion genomic DNA library [J].
Ding, DQ ;
Tomita, Y ;
Yamamoto, A ;
Chikashige, Y ;
Haraguchi, T ;
Hiraoka, Y .
GENES TO CELLS, 2000, 5 (03) :169-190
[14]   DNA double-strand break repair in cell-free extracts from Ku80-deficient cells: implications for Ku serving as an alignment factor in non-homologous DNA end joining [J].
Feldmann, E ;
Schmiemann, V ;
Goedecke, W ;
Reichenberger, S ;
Pfeiffer, P .
NUCLEIC ACIDS RESEARCH, 2000, 28 (13) :2585-2596
[15]   Transfer of a mitochondrial DNA fragment to MCOLN1 causes an inherited case of mucoliplidosis IV [J].
Goldin, E ;
Stahl, S ;
Cooney, AM ;
Kaneski, CR ;
Gupta, S ;
Brady, RO ;
Ellis, JR ;
Schiffmann, R .
HUMAN MUTATION, 2004, 24 (06) :460-465
[16]   Non-homologous DNA end joining in plant cells is associated with deletions and filler DNA insertions [J].
Gorbunova, V ;
Levy, AA .
NUCLEIC ACIDS RESEARCH, 1997, 25 (22) :4650-4657
[17]   OBSERVATIONS ON INTEGRATIVE TRANSFORMATION IN SCHIZOSACCHAROMYCES-POMBE [J].
GRIMM, C ;
KOHLI, J .
MOLECULAR & GENERAL GENETICS, 1988, 215 (01) :87-93
[18]   Ku70-deficient embryonic stem cells have increased ionizing radiosensitivity, defective DNA end-binding activity, and inability to support V(D)J recombination [J].
Gu, YS ;
Jin, SF ;
Gao, YJ ;
Weaver, DT ;
Alt, FW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (15) :8076-8081
[19]   Impact of the KU80 pathway on NHEJ-induced genome rearrangements in mammalian cells [J].
Guirouilh-Barbat, J ;
Huck, S ;
Bertrand, P ;
Pirzio, L ;
Desmaze, C ;
Sabatier, L ;
Lopez, BS .
MOLECULAR CELL, 2004, 14 (05) :611-623
[20]   Molecular analysis of telomere fusions in Arabidopsis:: multiple pathways for chromosome end-joining [J].
Heacock, M ;
Spangler, E ;
Riha, K ;
Puizina, J ;
Shippen, DE .
EMBO JOURNAL, 2004, 23 (11) :2304-2313