REPAIR OF DNA DOUBLE-STRAND BREAKS INDUCED IN SACCHAROMYCES-CEREVISIAE USING DIFFERENT GAMMA-RAY DOSE-RATES - A PULSED-FIELD GEL-ELECTROPHORESIS ANALYSIS

被引:13
作者
DARDALHON, M [1 ]
NOHTURFFT, A [1 ]
MENIEL, V [1 ]
AVERBECK, D [1 ]
机构
[1] INST CURIE,CNRS,URA 1292,F-75231 PARIS 05,FRANCE
关键词
D O I
10.1080/09553009414550361
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
We investigated the effects of gamma-ray exposures at high dose-rate (HDR, 23.2 Gy/min) and low dose-rate (LDR, 0.4.7 Gy/min) on survival and the induction of DNA double-strand breaks (dsb) in a diploid wild-type (D7) and the repair-deficient mutant strain rad52/rad52 of Saccharomyces cerevisiae. Analysis by pulsed-field gel electrophoresis (PFGE) using a contour homogeneous electric field apparatus revealed that, at HDR, in the range 0-400 Gy, dsb are induced as a linear function of gamma-ray dose. Liquid holding recovery in non-nutrient medium (LHR) for 48 h of wild-type cells treated at HDR, significantly increased survival and reduced the yield of dsb. Such changes did not occur in rad52/rad52 cells defective in the repair of dsb. Thus, in gamma-irradiated wild-type cells, an efficient repair of dsb is taking place during LHR. Treatments of wildtype cells at LDR resulted in higher survival and an approximately two-fold lower yield of dsb than at HDR. Such a dose-rate effect was absent in rad52/rad52 cells suggesting that, in wild-type cells during LDR exposures, significant amounts of dsb can be repaired. This repair could be very much accentuated by 48-h LHR of wild-type cells treated at LDR. The relationship observed between gamma-ray survival and dsb repair clearly indicates that increases in survival of wild-type cells, during LDR as compared with HDR exposures and after LHR, are strongly related to the repair of dsb.
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页码:307 / 314
页数:8
相关论文
共 46 条
[1]   CALIBRATION OF PULSED FIELD GEL-ELECTROPHORESIS FOR MEASUREMENT OF DNA DOUBLE-STRAND BREAKS [J].
AGER, DD ;
DEWEY, WC .
INTERNATIONAL JOURNAL OF RADIATION BIOLOGY, 1990, 58 (02) :249-259
[2]   MEASUREMENT OF RADIATION-INDUCED DNA DOUBLE-STRAND BREAKS BY PULSED-FIELD GEL-ELECTROPHORESIS [J].
AGER, DD ;
DEWEY, WC ;
GARDINER, K ;
HARVEY, W ;
JOHNSON, RT ;
WALDREN, CA .
RADIATION RESEARCH, 1990, 122 (02) :181-187
[3]  
AHN SY, 1991, INT J RADIAT BIOL, V59, P651
[4]   THE SEQUENCE OF THE DNAS CODING FOR THE MATING-TYPE LOCI OF SACCHAROMYCES-CEREVISIAE [J].
ASTELL, CR ;
AHLSTROMJONASSON, L ;
SMITH, M ;
TATCHELL, K ;
NASMYTH, KA ;
HALL, BD .
CELL, 1981, 27 (01) :15-23
[5]  
BERTSCHE U, 1978, RADIAT RES, V76, P349, DOI 10.2307/3574785
[6]   CHEF ELECTROPHORESIS, A SENSITIVE TECHNIQUE FOR THE DETERMINATION OF DNA DOUBLE-STRAND BREAKS [J].
BLOCHER, D ;
EINSPENNER, M ;
ZAJACKOWSKI, J .
INTERNATIONAL JOURNAL OF RADIATION BIOLOGY, 1989, 56 (04) :437-448
[7]   SEPARATION OF CHROMOSOMAL DNA-MOLECULES FROM YEAST BY ORTHOGONAL-FIELD-ALTERNATION GEL-ELECTROPHORESIS [J].
CARLE, GF ;
OLSON, MV .
NUCLEIC ACIDS RESEARCH, 1984, 12 (14) :5647-5664
[8]   SEPARATION OF LARGE DNA-MOLECULES BY CONTOUR-CLAMPED HOMOGENEOUS ELECTRIC-FIELDS [J].
CHU, G ;
VOLLRATH, D ;
DAVIS, RW .
SCIENCE, 1986, 234 (4783) :1582-1585
[9]   MODULATION OF RESTRICTION ENZYME-INDUCED DAMAGE BY CHEMICALS THAT INTERFERE WITH CELLULAR-RESPONSES TO DNA DAMAGE - A CYTOGENETIC AND PULSED-FIELD GEL ANALYSIS [J].
CHUNG, HW ;
PHILLIPS, JW ;
WINEGAR, RA ;
PRESTON, RJ ;
MORGAN, WF .
RADIATION RESEARCH, 1991, 125 (01) :107-113
[10]   ANALYSIS OF DNA DOUBLE STRAND BREAKAGE AND REPAIR USING ORTHOGONAL FIELD ALTERNATION GEL-ELECTROPHORESIS [J].
CONTOPOULOU, CR ;
COOK, VE ;
MORTIMER, RK .
YEAST, 1987, 3 (02) :71-76