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Effects of anthramycin and actinomycin on RNA synthesis patterns in L1210 cells
Author(s) -
Kann Herbert E.,
Kohn Kurt W.
Publication year - 1972
Publication title -
journal of cellular physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.529
H-Index - 174
eISSN - 1097-4652
pISSN - 0021-9541
DOI - 10.1002/jcp.1040790303
Subject(s) - rna , uridine , transcription (linguistics) , nucleoplasm , dactinomycin , chemistry , dna , biochemistry , biology , microbiology and biotechnology , gene , nucleolus , cytoplasm , linguistics , philosophy
Abstract Anthramycin and actinomycin D, two different types of DNA‐binding antibiotics, were compared for their effects on RNA synthesis in suspension cultures of mouse leukemia L1210 cells. RNA was labeled with radioactive uridine and selective effects on the synthesis of different classes of RNA were studied by sucrose gradient sedimentation of RNA purified from whole cells or from nucleolar and nucleoplasmic fractions. Two major differences were noted. (1) Whereas actinomycin produced two phases in the inhibition of uridine incorporation, the rapid phase being complete within a few minutes, anthramycin produced only a slow progressive inhibition. (2) Whereas actinomycin selectively inhibits nucleolar 45s RNA synthesis, anthramycin inhibits this RNA equally to the inhibition of the same size RNA in the nucleoplasm. Both antibiotics caused a shift towards lower molecular weight (slower sedimentation) in the distribution of nucleoplasmic RNA molecules synthesized in the presence of drug. When the two antibiotics were compared at concentrations producing equal extents of inhibition of nucleoplasmic RNA synthesis, anthryamycin produced the greater shift. The shift in sedimentation anthramycin produced the greater shift. The shift in sedimentation was not due to a slowing of RNA chain growth rate, since the change in sedimentation persisted when uridine incorporation time was increased so as to compensate for the reduction in RNA synthesis rate. The selective inhibition of nucleolar RNA synthesis by actinomycin could be due to possible differences in the properties of the different RNA polymerases, or to differences in the initiation rates for transcription. The absence of selectivity in the case of anthramycin might be related to the near irreversibility of its binding to DNA. The shift towards lower molecular weight of the RNA synthesized is compatible with (but does not constitute strong evidence for) premature termination of RNA chains.