Cell surface cAMP receptors (cARs) have been implicated in multiple aspects of development in Dictyostelium. Antisense mutagenesis has recently provided strong evidence that cARs are necessary for aggregation (Klein et al., 1988. Science (Wash. DC). 241:1467-1472). We show here that the expression of cAR1 antisense mRNA which prevents the appearance of cAR1 antigen also prevents the expression of cAMP-binding activity and blocks multiple cAMP-mediated responses. Chemotactic sensitivity to cAMP was lost as were stimulus-induced cAMP and cGMP production. Furthermore, the expression of developmentally regulated marker genes, dependent on repeated cAMP stimulation, was altered. As a result, the developmental program was severely impaired; most of the cells failed to aggregate and undergo further differentiation.
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1 May 1990
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May 01 1990
Surface cAMP receptors mediate multiple responses during development in Dictyostelium: evidenced by antisense mutagenesis.
T J Sun,
T J Sun
Department of Biological Chemistry, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205.
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P J Van Haastert,
P J Van Haastert
Department of Biological Chemistry, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205.
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P N Devreotes
P N Devreotes
Department of Biological Chemistry, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205.
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T J Sun
Department of Biological Chemistry, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205.
P J Van Haastert
Department of Biological Chemistry, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205.
P N Devreotes
Department of Biological Chemistry, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205.
Online ISSN: 1540-8140
Print ISSN: 0021-9525
J Cell Biol (1990) 110 (5): 1549–1554.
Citation
T J Sun, P J Van Haastert, P N Devreotes; Surface cAMP receptors mediate multiple responses during development in Dictyostelium: evidenced by antisense mutagenesis.. J Cell Biol 1 May 1990; 110 (5): 1549–1554. doi: https://doi.org/10.1083/jcb.110.5.1549
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