ACHILLES HEEL CLEAVAGE - CREATION OF RARE RESTRICTION SITES IN LAMBDA-PHAGE GENOMES AND EVALUATION OF ADDITIONAL OPERATORS, REPRESSORS AND RESTRICTION MODIFICATION SYSTEMS

被引:14
作者
GRIMES, E [1 ]
KOOB, M [1 ]
SZYBALSKI, W [1 ]
机构
[1] UNIV WISCONSIN,MCARDLE LAB CANC RES,MADISON,WI 53706
关键词
bacteriophages; λ; and; 434; DNA-binding proteins; lacI gene mutants; methyltransferase; plasmids; Recombinant DNA; restriction/modification system; synthetic operator;
D O I
10.1016/0378-1119(90)90432-Q
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
A novel technique for the creation of rare restriction sites was described by Koob et al. [Science 241 (1988) 1084-1086]. This technique, Achilles' heel cleavage (AC), relies on the use of a bound repressor molecule to protect only one of many identical restriction sites from a modification methyltransferase that inactivates all other restriction sites. The technique was applied to a small plasmid and shown to work efficiently with two repressor/operator systems: lac repressor/lacO operator and λ repressor/λoL 1 operator. Here, we have extended these results to a lac operator carried by a much larger vector, namely a 44-kb phage λ construct. In addition, we have evaluated the effect of altering the stability of the lac repressor/lac operator complex by varying both the operator and the repressor. We have also evaluated several more restriction/modification systems (MboI, Dam, MspI and AluI) in addition to HhaII and HaeII used earlier. Finally, we extended the AC technique to a third system, that of the phage 434 repressor and a synthetic 434 operator. From our results we conclude that the AC method should be applicable to the mapping of large genomes and to measuring the strength of operator-repressor interactions. AC could also be applied to identifying and evaluating many different DNA-binding proteins and their sites of action. © 1990.
引用
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页码:1 / 7
页数:7
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