## Abstract N^6^,O^2′^‐dibutyryl adenosine 3′,5′‐monophosphate kills cultured mouse lymphosarcoma cells, but not resistant mutants derived by a single‐step clonal selection. Resistant clones lack the cyclic AMP binding proteins present in wild type, cyclic AMP sensitive clones. Both endogenous cycl
Somatic genetic analysis of cyclic AMP action: Selection of unresponsive mutants
✍ Scribed by Philip Coffino; Henry R. Bourne; Gordon M. Tomkins
- Publisher
- John Wiley and Sons
- Year
- 1975
- Tongue
- English
- Weight
- 546 KB
- Volume
- 85
- Category
- Article
- ISSN
- 0021-9541
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✦ Synopsis
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 × 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.
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