TY - JOUR
T1 - Achilles' heel cleavage
T2 - creation of rare restriction sites in λ phage genomes and evaluation of additional operators, repressors and restriction/modification systems
AU - Grimes, Eric
AU - Koob, Michael
AU - Szybalski, Waclaw
PY - 1990/5/31
Y1 - 1990/5/31
N2 - 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.
AB - 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.
KW - DNA-binding proteins
KW - Recombinant DNA
KW - bacteriophages λ and 434
KW - lacI gene mutants
KW - methyltransferase
KW - plasmids
KW - restriction/modification system
KW - synthetic operator
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U2 - 10.1016/0378-1119(90)90432-Q
DO - 10.1016/0378-1119(90)90432-Q
M3 - Article
C2 - 2165969
AN - SCOPUS:0025333642
SN - 0378-1119
VL - 90
SP - 1
EP - 7
JO - Gene
JF - Gene
IS - 1
ER -