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PMID: 167036 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Somatic genetic analysis of cyclic AMP action: selection of unresponsive mutants.

Journal of cellular physiology ·Vol. 85 ·No. 3 ·1975-06-00 ·Pages 603-10

Coffino P, Bourne HR, Tomkins GM

Abstract

Dibutyryl cyclic AMP and theophylline kill S49.1 mouse lymphoma tissue culture cells. When cells are grown in soft agar with these drugs, the few clones that survive are resistant to cytolysis. The rate of mutation to resistance is 1-3 times 10-7/cell/generation in both diploid and tetraploid cells. The incidence of mutants is increased by treatment with a chemical mutagen, ICR 191. The mutation is consistently associated with greatly reduced or absent cytoplasmic cyclic AMP binding protein. These results suggest that a somatic mutation leads to a defect of the protein kinase regulatory subunit and that activity of this kinase is required for induction of cell death by cyclic AMP.

MeSH Terms
Animals Bucladesine/pharmacology Cell Line Chromosomes/analysis Clone Cells Cyclic AMP/metabolism,physiology Diploidy Drug Resistance Lymphoma/metabolism,pathology Mice Molecular Biology Mutation Polyploidy Theophylline/pharmacology
Chemicals
Bucladesine Theophylline Cyclic AMP
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Coffino P
Bourne H R
Tomkins G M
Article Info
Journal
Journal of cellular physiology
Abbr.
J Cell Physiol
ISSN
0021-9541
Published
1975-06-00
Pages
603-10
Language
English
Region
United States
NLM ID
0050222
Subset
IM
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