Nucleic Acids Research, 1987, Vol. 15, No. 10 4179-4191
© 1987
Articles |
Characterization of xenobiotic responsive elements upstream from the drug-metabolizing cytochrome P-450c gene: a similarity to glucocorticoid regulatory elements
Department of Biochemistry, Cancer Institute, Japanese Foundation for Cancer Research 1-37-1, Kamiikebukuro, Toshima-ku, Tokyo 170, Japan
Received March 10, 1987. Revised April 23, 1987. Accepted April 23, 1987.
The DNA element governing the inducible expression of drug-metabolizing P-450c gene by xenobiotic treatments was investigated by gene transfer methods. A variety of dissected fragments from -844 to -1140bp region which was essential for the inducibility of P-450c gene were placed on the hetero-logous SV40 promoter for testing the inducibility. Mapping studies in combination with gel retardation assay defined the presence of the two xenobiotic responsive elements(XRE, XRE1, -1007 - -1021bp; XRE2, -1088 - -1092bp) composed of about 15 nucleotides which expressed the enhancer activity in response to xenobiotic inducers. The two XREs share 10 nucleotides in common out of 15 as expressed in the sequence CG/CTG/CC/TTG/CTCACGCT/AA and are arranged in the inverse orientation. They are different from DREs(drug responsive element) proposed previously(Sogawa, K. et al. Proc. Natl. Acad. Sci. 83, 8044–8048(1986)) and expressed a strong enhancer activity in response to 3-methylcholanthrene. The XRE shows a significant homology with glucocort.icoid regulatory elements and apparently needs normal functions of a putative xenobiotic receptor for the inducible enhancer activity.
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