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Vol. 61, Issue 4, 795-799, April 2002
Division of Biochemistry, Department of Pharmaceutical Biosciences,
Faculty of Pharmacy, Biomedical Centrum, University of Uppsala, Sweden
(F.R.-M., T.G., M.A.L.); and Department of Medical Biophysics,
University of Toronto, Sunnybrook and Women's College Health Science
Centre, Toronto, Ontario, Canada (Y.B.-D.).
The heterogeneous nuclear ribonucleoprotein A1 (hnRNP A1) functions in
the packaging of nascent RNA polymerase II transcripts and participates
in a variety of nuclear and cytoplasmic processes that modulate gene
expression. The RNA binding characteristics of hnRNP A1 suggest that it
can modulate the expression of specific genes, but little is known
about its possible targets in vivo. In this article, we show that hnRNP
A1 interacts with the transcript of a cytochrome P450 gene,
Cyp2a5, induced by xenobiotics and during liver damage.
Binding of the hnRNP A1 to CYP2A5 mRNA was demonstrated by
immunoprecipitation of the xenobiotic-stimulated (37/39 kDa) CYP2A5
mRNA-protein complex with a monoclonal anti-hnRNP A1 antibody, by
partial trypsin digestion of the complex, and by showing that the
RNA-protein complex is not formed with protein extracts from cells
lacking the hnRNP A1. We also show that a specific hepatotoxic inducer
of the Cyp2a5 gene, pyrazole, increases the cytoplasmic
levels of hnRNP A1 in vivo. Finally, we show that hnRNP A1 can be
overexpressed in mouse primary hepatocytes, leading to an accumulation
of the CYP2A5 mRNA. Collectively, these results indicate that the hnRNP
A1 is an important regulator of the Cyp2a5 gene.
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