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Effect of 5-bromodeoxyuridine on heterogeneous nuclear RNA in rat hepatoma cells
Author(s) -
Heather W. Weber,
Robert H. Stellwagen
Publication year - 1979
Publication title -
nucleic acids research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 9.008
H-Index - 537
eISSN - 1362-4954
pISSN - 0305-1048
DOI - 10.1093/nar/6.4.1731
Subject(s) - biology , precursor mrna , microbiology and biotechnology , rna , uridine , bromodeoxyuridine , population , cell nucleus , gel electrophoresis , biochemistry , ficoll , centrifugation , differential centrifugation , cell growth , gene , peripheral blood mononuclear cell , demography , sociology , rna splicing , in vitro
Heterogeneous nuclear RNA HnRNA) was isolated from untreated and 5-bromodeoxyuridine (BrdUrd) treated hepatoma tissue culture (HTC) cells. analysis of this RNA by either electrophoresis on polyacrylamide-agarose gels or centrifugation in sucrose gradients demonstrated that BrdUrd caused a shift in the labeled HnRNA population toward a smaller size distribution. This effect was produced by concentrations of BrdUrd which specifically lower the level of the differentiated enzyme tyrosine aminotransferase, but do not greatly affect cell growth. Differential binding to oligo(dT) cellulose was used to fractionate HnRNA further into classes containing poly(A) (alpha), oligo(A) (beta) or neither category of A-rich sequences (gamma). BrdUrd did not alter the relative rates of uridine incorporation into the three classes. The shift in the labeled HnRNA population due to BrdUrd was observed in all three subclasses of HnRNA.

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