1S911-mediated intramolecular transposition is naturally temperature sensitive

被引:25
作者
Haren, L [1 ]
Betermier, M [1 ]
Polard, P [1 ]
Chandler, M [1 ]
机构
[1] CNRS, UPR9007, LAB MICROBIOL & GENET MOL, F-31062 TOULOUSE, FRANCE
关键词
D O I
10.1046/j.1365-2958.1997.4951854.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
It is shown here that the bacterial insertion sequence IS911 exhibits a temperature-sensitive transposition phenotype. Previous results have demonstrated that elevated levels of the IS911 transposase OrfAB generate significant quantities of a figure-eight form, created by cleavage and circularization of one of the transposon strands, and of an excised circular form, in which both transposon strands have been circularized. We show here that the level of both types of molecule observed in vivo was greatly reduced at 42 degrees C compared with 37 degrees C. On the other hand, reducing the temperature to 30 degrees C resulted in a significant increase in production. Transposition activity at this temperature was sufficiently high to permit detection in vivo of an excised circular form of a defective single IS911 chromosomal copy when OrfAB is supplied in trans. A similar temperature-activity profile is observed for a cell-free reaction that uses partially purified OrfAB and generates the figure-eight form uniquely. Moreover, two point mutants of OrfAB were obtained, which render the reactions partially temperature resistant both in vivo and in vitro. These results suggest that some property of transposase itself is sensitive to elevated temperatures.
引用
收藏
页码:531 / 540
页数:10
相关论文
共 31 条
[1]   Retroviral integrase, putting the pieces together [J].
Andrake, MD ;
Skalka, AM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (33) :19633-19636
[2]   Assembly of a strong promoter following IS911 circularization and the role of circles in transposition [J].
Bao, TH ;
Betermier, M ;
Polard, P ;
Chandler, M .
EMBO JOURNAL, 1997, 16 (11) :3357-3371
[3]   IDENTIFICATION AND SEQUENCE OF GENE DICB - TRANSLATION OF THE DIVISION INHIBITOR FROM AN IN-PHASE INTERNAL START [J].
CAM, K ;
BEJAR, S ;
GIL, D ;
BOUCHE, JP .
NUCLEIC ACIDS RESEARCH, 1988, 16 (14) :6327-6338
[4]  
Campbell Julie H., 1994, Current Opinion in Lipidology, V5, P323, DOI 10.1097/00041433-199410000-00003
[5]   TRANSLATIONAL FRAMESHIFTING IN THE CONTROL OF TRANSPOSITION IN BACTERIA [J].
CHANDLER, M ;
FAYET, O .
MOLECULAR MICROBIOLOGY, 1993, 7 (04) :497-503
[6]  
CORNELIS G, 1980, J GEN MICROBIOL, V117, P243
[7]   NOVEL REARRANGEMENTS OF IS30 CARRYING PLASMIDS LEADING TO THE REACTIVATION OF GENE-EXPRESSION [J].
DALRYMPLE, B .
MOLECULAR & GENERAL GENETICS, 1987, 207 (2-3) :413-420
[8]   DETECTION OF CHEMICALS THAT STIMULATE TN9 TRANSPOSITION IN ESCHERICHIA-COLI-K12 [J].
DATTA, AR ;
RANDOLPH, BW ;
ROSNER, JL .
MOLECULAR & GENERAL GENETICS, 1983, 189 (02) :245-250
[9]  
DIAZ JJ, 1991, BIOTECHNIQUES, V11, P204
[10]  
GALAS DJ, 1989, MOBILE DNA, P109