Expression and subcellular distribution of mouse cytochrome P1-450 mRNA as determined by molecular hybridization with cloned P1-450 DNA |
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Authors: | Y T Chen M Negishi |
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Affiliation: | Developmental Pharmacology Branch National Institute of Child Health and Human Development National Institutes of Health, Bethesda, Maryland 20205 USA |
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Abstract: | Cytochrome P1-450 (P1-450) is defined as that cytochrome most closely associated with 3-methylcholanthrene (MC)-induced aryl hydrocarbon hydroxylase (AHH) activity. Recently a cloned DNA sequence (clone 46) was shown to represent a portion of the P1-450 structural gene [Negishi : 800–804 (1981)]. Poly(A+)-enriched RNA was isolated from total liver homogenate, membrane-bound polysomes and from free polysomes at various times after MC treatment of -responsive (B6) and -nonresponsive (D2) inbred mice. The poly(A+)-enriched RNA was separated by methylmercury-agarose gel electrophoresis and hybridized to nick-translated [32P]DNA from clone 46. By means of this RNA-DNA hybridization, only 6% of total polysomal P1-450 mRNA exists in free polysomes after 24 h of MC treatment. The data indicate that the endoplasmic reticulum is the principal site of synthesis for this integral microsomal protein.Studies of induction kinetics following MC treatment provided the evidence of the rapid increase of total liver and membrane bound P1-450 mRNA preceding the synthesis of apo-P1-450 and the increase of AHH activity. |
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Keywords: | MC 3-methylcholanthrene B6 D2 AHH aryl hydrocarbon hydroxylase |
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