Evidence that 2‐allyl‐2‐isopropylacetamide, phenobarbital and 3,5‐diethoxycarbonyl‐1,4‐dihydrocollidine induce the same cytochrome P 450 mRNA in chick embryo liver
The induction of cytochrome P 450 in chick embryo liver has been studied using three different porphyrinogenic drugs, 2‐allyl‐2‐isopropylacetamide, 3,5‐diethoxycarbonyl‐1,4‐dihydrocollidine and phenobarbital. Pulse‐labelling studies have shown that for each drug the cytochrome P 450 synthesised eith...
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Published in: | European journal of biochemistry Vol. 136; no. 2; pp. 327 - 332 |
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Main Authors: | , , , , |
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Language: | English |
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01-11-1983
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Abstract | The induction of cytochrome P
450
in chick embryo liver has been studied using three different porphyrinogenic drugs, 2‐allyl‐2‐isopropylacetamide, 3,5‐diethoxycarbonyl‐1,4‐dihydrocollidine and phenobarbital. Pulse‐labelling studies have shown that for each drug the cytochrome P
450
synthesised either
in ovo
or in a wheat germ translation system reacted immunologically with antibody raised against the purified 2‐allyl‐2‐isopropylacetamide‐induced enzyme (
M
r
= 50 000).
To investigate whether this is due to the three drugs inducing the same protein or different proteins with common immunological determinants, nucleic acid hybridization studies have been carried out using a recently characterised 2‐allyl‐2‐isopropylacetamide‐induced cytochrome P
450
cloned cDNA probe [Brooker, J. D. et al. (1982)
Eur. J. Biochem. 129
, 325–333]. It has been shown that the mRNA induced by each drug hybridizes with this probe and all are of similar size. The melting profile of the mRNA · cDNA hybrids indicates that the mRNAs induced by the three drugs have at least 98% homology with the cDNA probe.
Restriction endonuclease digestions of total chick embryo genomal DNA and a chick cytochrome P
450
genomal clone indicates that the cytochrome P
450
gene homologous with the cDNA probe is represented in the genome only once.
These results strongly suggest that the three drugs cause increased levels of the same cytochrome P
450
mRNA, possibly due to enhanced expression of the same gene.
Results are also presented which show that other cytochrome‐P
450
‐inducing drugs, 3‐methylcholanthrene, β‐naphthoflavone or pregnenolone‐16 α‐carbonitrile do not increase the level of the 2‐allyl‐2‐isopropylacetamide‐inducible mRNA but rather reduce it to a level which was lower than that of the untreated controls. |
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AbstractList | The induction of cytochrome P
450
in chick embryo liver has been studied using three different porphyrinogenic drugs, 2‐allyl‐2‐isopropylacetamide, 3,5‐diethoxycarbonyl‐1,4‐dihydrocollidine and phenobarbital. Pulse‐labelling studies have shown that for each drug the cytochrome P
450
synthesised either
in ovo
or in a wheat germ translation system reacted immunologically with antibody raised against the purified 2‐allyl‐2‐isopropylacetamide‐induced enzyme (
M
r
= 50 000).
To investigate whether this is due to the three drugs inducing the same protein or different proteins with common immunological determinants, nucleic acid hybridization studies have been carried out using a recently characterised 2‐allyl‐2‐isopropylacetamide‐induced cytochrome P
450
cloned cDNA probe [Brooker, J. D. et al. (1982)
Eur. J. Biochem. 129
, 325–333]. It has been shown that the mRNA induced by each drug hybridizes with this probe and all are of similar size. The melting profile of the mRNA · cDNA hybrids indicates that the mRNAs induced by the three drugs have at least 98% homology with the cDNA probe.
Restriction endonuclease digestions of total chick embryo genomal DNA and a chick cytochrome P
450
genomal clone indicates that the cytochrome P
450
gene homologous with the cDNA probe is represented in the genome only once.
These results strongly suggest that the three drugs cause increased levels of the same cytochrome P
450
mRNA, possibly due to enhanced expression of the same gene.
Results are also presented which show that other cytochrome‐P
450
‐inducing drugs, 3‐methylcholanthrene, β‐naphthoflavone or pregnenolone‐16 α‐carbonitrile do not increase the level of the 2‐allyl‐2‐isopropylacetamide‐inducible mRNA but rather reduce it to a level which was lower than that of the untreated controls. |
Author | MAY, Brian K. ELLIOTT, William H. BROOKER, John D. SRIVASTAVA, Gopesh BORTHWICK, Iain A. |
Author_xml | – sequence: 1 givenname: John D. surname: BROOKER fullname: BROOKER, John D. – sequence: 2 givenname: Gopesh surname: SRIVASTAVA fullname: SRIVASTAVA, Gopesh – sequence: 3 givenname: Iain A. surname: BORTHWICK fullname: BORTHWICK, Iain A. – sequence: 4 givenname: Brian K. surname: MAY fullname: MAY, Brian K. – sequence: 5 givenname: William H. surname: ELLIOTT fullname: ELLIOTT, William H. |
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CitedBy_id | crossref_primary_10_1002_bies_950040512 crossref_primary_10_1016_S0300_483X_02_00145_2 crossref_primary_10_1111_j_1432_1033_1984_tb08435_x crossref_primary_10_1016_0006_2952_88_90585_0 crossref_primary_10_1016_S0021_9258_18_67676_8 crossref_primary_10_3109_00498258909043165 crossref_primary_10_1016_0006_2952_89_90212_8 crossref_primary_10_1016_0006_2952_89_90192_5 crossref_primary_10_1016_0742_8413_90_90063_F crossref_primary_10_1016_0006_291X_84_91396_2 crossref_primary_10_1016_0003_2697_89_90129_2 crossref_primary_10_1016_0006_291X_86_90456_0 crossref_primary_10_1016_0020_711X_89_90235_8 crossref_primary_10_1016_S0742_8413_98_10031_2 crossref_primary_10_1016_S0021_9258_18_45477_4 |
Cites_doi | 10.1016/S0021-9258(18)96783-9 10.1016/S0021-9258(19)69128-3 10.1093/oxfordjournals.jbchem.a132996 10.1016/0092-8674(79)90328-3 10.1073/pnas.80.5.1169 10.1093/oxfordjournals.jbchem.a133187 10.1111/j.1432-1033.1980.tb05992.x 10.1038/227680a0 10.1073/pnas.79.9.2793 10.1042/bj1240767 10.1016/S0021-9258(17)34461-7 10.1016/S0021-9258(18)34039-0 10.1016/0014-5793(82)80771-0 10.1016/S0021-9258(17)30058-3 10.1111/j.1432-1033.1982.tb07055.x 10.1016/S0021-9258(18)33822-5 10.1111/j.1432-1033.1983.tb07093.x 10.1016/S0021-9258(19)68292-X 10.1073/pnas.77.9.5201 |
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References | Maniatis T. (e_1_2_3_18_2) 1982 e_1_2_3_19_2 Matteis F. (e_1_2_3_2_2) 1978 e_1_2_3_5_2 e_1_2_3_4_2 e_1_2_3_16_2 e_1_2_3_3_2 Baron J. (e_1_2_3_11_2) 1982; 257 e_1_2_3_17_2 e_1_2_3_9_2 e_1_2_3_22_2 Harada N. (e_1_2_3_15_2) 1981; 89 e_1_2_3_7_2 Rifkind A. B. (e_1_2_3_8_2) 1982; 257 e_1_2_3_13_2 e_1_2_3_6_2 e_1_2_3_14_2 Elshourbagy N. A. (e_1_2_3_12_2) 1981; 256 e_1_2_3_20_2 e_1_2_3_10_2 e_1_2_3_21_2 |
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Title | Evidence that 2‐allyl‐2‐isopropylacetamide, phenobarbital and 3,5‐diethoxycarbonyl‐1,4‐dihydrocollidine induce the same cytochrome P 450 mRNA in chick embryo liver |
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