TY - JOUR
T1 - Ability of various alkylating agents to induce adaptive and SOS responses
T2 - A study with lacZ fusion
AU - Otsuka, Masanori
AU - Nakabeppu, usaku
AU - Sekiguchi, Mutsuo
PY - 1985/9
Y1 - 1985/9
N2 - We used alkA′-lacZ′ and umuC′-lacZ′ fused genes and determined the ability of various alkylating agents to induce adaptive and SOS responses. The degree of induction of expression of these genes was quantitatively measured by a simple colorimetric assay of ß-galactosidase activity. SN1 type methylating agents, such as N-methyl-N′-nitro-N-nitrosoguanidine and B-methyl-N-nitrosourea, were more effective inducers for the alkA than for the umuC system, while SN1 type ethylating agents, such as N-ethyl-N′-nitro-N-nitrosoguanidine and N-ethyl-N-nitrosourea, were more potent inducers for the umuC than for the alkA system. Similar but less striking effects on the two systems were obtained with SN2 type alkylating agents.
AB - We used alkA′-lacZ′ and umuC′-lacZ′ fused genes and determined the ability of various alkylating agents to induce adaptive and SOS responses. The degree of induction of expression of these genes was quantitatively measured by a simple colorimetric assay of ß-galactosidase activity. SN1 type methylating agents, such as N-methyl-N′-nitro-N-nitrosoguanidine and B-methyl-N-nitrosourea, were more effective inducers for the alkA than for the umuC system, while SN1 type ethylating agents, such as N-ethyl-N′-nitro-N-nitrosoguanidine and N-ethyl-N-nitrosourea, were more potent inducers for the umuC than for the alkA system. Similar but less striking effects on the two systems were obtained with SN2 type alkylating agents.
UR - http://www.scopus.com/inward/record.url?scp=0021933142&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0021933142&partnerID=8YFLogxK
U2 - 10.1016/0167-8817(85)90005-7
DO - 10.1016/0167-8817(85)90005-7
M3 - Article
C2 - 2993877
AN - SCOPUS:0021933142
SN - 0167-8817
VL - 146
SP - 149
EP - 154
JO - Mutation Research DNA Repair Reports
JF - Mutation Research DNA Repair Reports
IS - 2
ER -