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. 1995 Jun 1;129(5):1251–1262. doi: 10.1083/jcb.129.5.1251

A density-sensing factor regulates signal transduction in Dictyostelium

PMCID: PMC2120463  PMID: 7775572

Abstract

Dictyostelium discoideum initiates development when cells overgrow their bacterial food source and starve. To coordinate development, the cells monitor the extracellular level of a protein, conditioned medium factor (CMF), secreted by starved cells. When a majority of the cells in a given area have starved, as signaled by CMF secretion, the extracellular level of CMF rises above a threshold value and permits aggregation of the starved cells. The cells aggregate using relayed pulses of cAMP as the chemoattractant. Cells in which CMF accumulation has been blocked by antisense do not aggregate except in the presence of exogenous CMF. We find that these cells are viable but do not chemotax towards cAMP. Videomicroscopy indicates that the inability of CMF antisense cells to chemotax is not due to a gross defect in motility, although both video and scanning electron microscopy indicate that CMF increases the frequency of pseudopod formation. The activations of Ca2+ influx, adenylyl cyclase, and guanylyl cyclase in response to a pulse of cAMP are strongly inhibited in cells lacking CMF, but are rescued by as little as 10 s exposure of cells to CMF. The activation of phospholipase C by cAMP is not affected by CMF. Northern blots indicate normal levels of the cAMP receptor mRNA in CMF antisense cells during development, while cAMP binding assays and Scatchard plots indicate that CMF antisense cells contain normal levels of the cAMP receptor. In Dictyostelium, both adenylyl and guanylyl cyclases are activated via G proteins. We find that the interaction of the cAMP receptor with G proteins in vitro is not measurably affected by CMF, whereas the activation of adenylyl cyclase by G proteins requires cells to have been exposed to CMF. CMF thus appears to regulate aggregation by regulating an early step of cAMP signal transduction.

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Selected References

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  1. Abe F., Maeda Y. Precise expression of the cAMP receptor gene, CAR1, during transition from growth to differentiation in Dictyostelium discoideum. FEBS Lett. 1994 Apr 11;342(3):239–241. doi: 10.1016/0014-5793(94)80509-1. [DOI] [PubMed] [Google Scholar]
  2. Bominaar A. A., Van Haastert P. J. Phospholipase C in Dictyostelium discoideum. Identification of stimulatory and inhibitory surface receptors and G-proteins. Biochem J. 1994 Jan 1;297(Pt 1):189–193. doi: 10.1042/bj2970189. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Bumann J., Wurster B., Malchow D. Attractant-induced changes and oscillations of the extracellular Ca++ concentration in suspensions of differentiating Dictyostelium cells. J Cell Biol. 1984 Jan;98(1):173–178. doi: 10.1083/jcb.98.1.173. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Clarke M., Dominguez N., Yuen I. S., Gomer R. H. Growing and starving Dictyostelium cells produce distinct density-sensing factors. Dev Biol. 1992 Aug;152(2):403–406. doi: 10.1016/0012-1606(92)90147-9. [DOI] [PubMed] [Google Scholar]
  5. Cubitt A. B., Carrel F., Dharmawardhane S., Gaskins C., Hadwiger J., Howard P., Mann S. K., Okaichi K., Zhou K., Firtel R. A. Molecular genetic analysis of signal transduction pathways controlling multicellular development in Dictyostelium. Cold Spring Harb Symp Quant Biol. 1992;57:177–192. doi: 10.1101/sqb.1992.057.01.023. [DOI] [PubMed] [Google Scholar]
  6. Devreotes P. N. G protein-linked signaling pathways control the developmental program of Dictyostelium. Neuron. 1994 Feb;12(2):235–241. doi: 10.1016/0896-6273(94)90267-4. [DOI] [PubMed] [Google Scholar]
  7. Dottin R. P., Bodduluri S. R., Doody J. F., Haribabu B. Signal transduction and gene expression in Dictyostelium discoideum. Dev Genet. 1991;12(1-2):2–5. doi: 10.1002/dvg.1020120103. [DOI] [PubMed] [Google Scholar]
  8. Drayer A. L., Van der Kaay J., Mayr G. W., Van Haastert P. J. Role of phospholipase C in Dictyostelium: formation of inositol 1,4,5-trisphosphate and normal development in cells lacking phospholipase C activity. EMBO J. 1994 Apr 1;13(7):1601–1609. doi: 10.1002/j.1460-2075.1994.tb06423.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Europe-Finner G. N., Newell P. C. Cyclic AMP stimulates accumulation of inositol trisphosphate in Dictyostelium. J Cell Sci. 1987 Mar;87(Pt 2):221–229. doi: 10.1242/jcs.87.2.221. [DOI] [PubMed] [Google Scholar]
  10. Europe-Finner G. N., Newell P. C. GTP analogues stimulate inositol trisphosphate formation transiently in Dictyostelium. J Cell Sci. 1987 May;87(Pt 4):513–518. doi: 10.1242/jcs.87.4.513. [DOI] [PubMed] [Google Scholar]
  11. Firtel R. A., van Haastert P. J., Kimmel A. R., Devreotes P. N. G protein linked signal transduction pathways in development: dictyostelium as an experimental system. Cell. 1989 Jul 28;58(2):235–239. doi: 10.1016/0092-8674(89)90837-4. [DOI] [PubMed] [Google Scholar]
  12. Gilman A. G. G proteins: transducers of receptor-generated signals. Annu Rev Biochem. 1987;56:615–649. doi: 10.1146/annurev.bi.56.070187.003151. [DOI] [PubMed] [Google Scholar]
  13. Gilman A. G. Transmembrane signaling, G proteins, and adenylyl cyclase. Harvey Lect. 1989;85:153–172. [PubMed] [Google Scholar]
  14. Gomer R. H., Firtel R. A. Cell-autonomous determination of cell-type choice in Dictyostelium development by cell-cycle phase. Science. 1987 Aug 14;237(4816):758–762. doi: 10.1126/science.3039657. [DOI] [PubMed] [Google Scholar]
  15. Gomer R. H., Yuen I. S., Firtel R. A. A secreted 80 x 10(3) Mr protein mediates sensing of cell density and the onset of development in Dictyostelium. Development. 1991 May;112(1):269–278. doi: 10.1242/dev.112.1.269. [DOI] [PubMed] [Google Scholar]
  16. Grabel L., Loomis W. F. Effector controlling accumulation of N-acetylglucosaminidase during development of Dictyostelium discoideum. Dev Biol. 1978 Jun;64(2):203–209. doi: 10.1016/0012-1606(78)90072-6. [DOI] [PubMed] [Google Scholar]
  17. Insall R., Kuspa A., Lilly P. J., Shaulsky G., Levin L. R., Loomis W. F., Devreotes P. CRAC, a cytosolic protein containing a pleckstrin homology domain, is required for receptor and G protein-mediated activation of adenylyl cyclase in Dictyostelium. J Cell Biol. 1994 Sep;126(6):1537–1545. doi: 10.1083/jcb.126.6.1537. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Jain R., Gomer R. H. A developmentally regulated cell surface receptor for a density-sensing factor in Dictyostelium. J Biol Chem. 1994 Mar 25;269(12):9128–9136. [PubMed] [Google Scholar]
  19. Jain R., Yuen I. S., Taphouse C. R., Gomer R. H. A density-sensing factor controls development in Dictyostelium. Genes Dev. 1992 Mar;6(3):390–400. doi: 10.1101/gad.6.3.390. [DOI] [PubMed] [Google Scholar]
  20. Janssens P. M., Van Haastert P. J. Molecular basis of transmembrane signal transduction in Dictyostelium discoideum. Microbiol Rev. 1987 Dec;51(4):396–418. doi: 10.1128/mr.51.4.396-418.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Kay R. R. cAMP and spore differentiation in Dictyostelium discoideum. Proc Natl Acad Sci U S A. 1982 May;79(10):3228–3231. doi: 10.1073/pnas.79.10.3228. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Kesbeke F., Snaar-Jagalska B. E., Van Haastert P. J. Signal transduction in Dictyostelium fgd A mutants with a defective interaction between surface cAMP receptors and a GTP-binding regulatory protein. J Cell Biol. 1988 Aug;107(2):521–528. doi: 10.1083/jcb.107.2.521. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Klein P. S., Sun T. J., Saxe C. L., 3rd, Kimmel A. R., Johnson R. L., Devreotes P. N. A chemoattractant receptor controls development in Dictyostelium discoideum. Science. 1988 Sep 16;241(4872):1467–1472. doi: 10.1126/science.3047871. [DOI] [PubMed] [Google Scholar]
  24. Konijn T. M. Microbiological assay of cyclic 3',5'-AMP. Experientia. 1970 Apr 15;26(4):367–369. doi: 10.1007/BF01896891. [DOI] [PubMed] [Google Scholar]
  25. Kumagai A., Hadwiger J. A., Pupillo M., Firtel R. A. Molecular genetic analysis of two G alpha protein subunits in Dictyostelium. J Biol Chem. 1991 Jan 15;266(2):1220–1228. [PubMed] [Google Scholar]
  26. Kumagai A., Pupillo M., Gundersen R., Miake-Lye R., Devreotes P. N., Firtel R. A. Regulation and function of G alpha protein subunits in Dictyostelium. Cell. 1989 Apr 21;57(2):265–275. doi: 10.1016/0092-8674(89)90964-1. [DOI] [PubMed] [Google Scholar]
  27. Kuwayama H., Ishida S., Van Haastert P. J. Non-chemotactic Dictyostelium discoideum mutants with altered cGMP signal transduction. J Cell Biol. 1993 Dec;123(6 Pt 1):1453–1462. doi: 10.1083/jcb.123.6.1453. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Mann S. K., Firtel R. A. Two-phase regulatory pathway controls cAMP receptor-mediated expression of early genes in Dictyostelium. Proc Natl Acad Sci U S A. 1989 Mar;86(6):1924–1928. doi: 10.1073/pnas.86.6.1924. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Mehdy M. C., Firtel R. A. A secreted factor and cyclic AMP jointly regulate cell-type-specific gene expression in Dictyostelium discoideum. Mol Cell Biol. 1985 Apr;5(4):705–713. doi: 10.1128/mcb.5.4.705. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Milne J. L., Coukell M. B. A Ca2+ transport system associated with the plasma membrane of Dictyostelium discoideum is activated by different chemoattractant receptors. J Cell Biol. 1991 Jan;112(1):103–110. doi: 10.1083/jcb.112.1.103. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. Milne J. L., Devreotes P. N. The surface cyclic AMP receptors, cAR1, cAR2, and cAR3, promote Ca2+ influx in Dictyostelium discoideum by a G alpha 2-independent mechanism. Mol Biol Cell. 1993 Mar;4(3):283–292. doi: 10.1091/mbc.4.3.283. [DOI] [PMC free article] [PubMed] [Google Scholar]
  32. Milne J. L., Wu L., Caterina M. J., Devreotes P. N. Seven helix cAMP receptors stimulate Ca2+ entry in the absence of functional G proteins in Dictyostelium. J Biol Chem. 1995 Mar 17;270(11):5926–5931. doi: 10.1074/jbc.270.11.5926. [DOI] [PubMed] [Google Scholar]
  33. Newell P. C., Europe-Finner G. N., Small N. V., Liu G. Inositol phosphates, G-proteins and ras genes involved in chemotactic signal transduction of Dictyostelium. J Cell Sci. 1988 Feb;89(Pt 2):123–127. doi: 10.1242/jcs.89.2.123. [DOI] [PubMed] [Google Scholar]
  34. Okaichi K., Cubitt A. B., Pitt G. S., Firtel R. A. Amino acid substitutions in the Dictyostelium G alpha subunit G alpha 2 produce dominant negative phenotypes and inhibit the activation of adenylyl cyclase, guanylyl cyclase, and phospholipase C. Mol Biol Cell. 1992 Jul;3(7):735–747. doi: 10.1091/mbc.3.7.735. [DOI] [PMC free article] [PubMed] [Google Scholar]
  35. Peters D. J., Cammans M., Smit S., Spek W., van Lookeren Campagne M. M., Schaap P. Control of cAMP-induced gene expression by divergent signal transduction pathways. Dev Genet. 1991;12(1-2):25–34. doi: 10.1002/dvg.1020120107. [DOI] [PubMed] [Google Scholar]
  36. Saxe C. L., 3rd, Johnson R., Devreotes P. N., Kimmel A. R. Multiple genes for cell surface cAMP receptors in Dictyostelium discoideum. Dev Genet. 1991;12(1-2):6–13. doi: 10.1002/dvg.1020120104. [DOI] [PubMed] [Google Scholar]
  37. Saxe C. L., 3rd, Klein P., Sun T. J., Kimmel A. R., Devreotes P. N. Structure and expression of the cAMP cell-surface receptor. Dev Genet. 1988;9(4-5):227–235. doi: 10.1002/dvg.1020090405. [DOI] [PubMed] [Google Scholar]
  38. Schaap P., Van Lookeren Campagne M. M., Van Driel R., Spek W., Van Haastert P. J., Pinas J. Postaggregative differentiation induction by cyclic AMP in Dictyostelium: intracellular transduction pathway and requirement for additional stimuli. Dev Biol. 1986 Nov;118(1):52–63. doi: 10.1016/0012-1606(86)90072-2. [DOI] [PubMed] [Google Scholar]
  39. Segall J. E. Behavioral responses of streamer F mutants of Dictyostelium discoideum: effects of cyclic GMP on cell motility. J Cell Sci. 1992 Mar;101(Pt 3):589–597. doi: 10.1242/jcs.101.3.589. [DOI] [PubMed] [Google Scholar]
  40. Snaar-Jagalska B. E., Kesbeke F., Van Haastert P. J. G-proteins in the signal-transduction pathways of Dictyostelium discoideum. Dev Genet. 1988;9(4-5):215–226. doi: 10.1002/dvg.1020090404. [DOI] [PubMed] [Google Scholar]
  41. Snaar-Jagalska B. E., Van Haastert P. J. Dictyostelium discoideum mutant synag 7 with altered G-protein-adenylate cyclase interaction. J Cell Sci. 1988 Oct;91(Pt 2):287–294. doi: 10.1242/jcs.91.2.287. [DOI] [PubMed] [Google Scholar]
  42. Sun T. J., Van Haastert P. J., Devreotes P. N. Surface cAMP receptors mediate multiple responses during development in Dictyostelium: evidenced by antisense mutagenesis. J Cell Biol. 1990 May;110(5):1549–1554. doi: 10.1083/jcb.110.5.1549. [DOI] [PMC free article] [PubMed] [Google Scholar]
  43. Theibert A., Devreotes P. N. Surface receptor-mediated activation of adenylate cyclase in Dictyostelium. Regulation by guanine nucleotides in wild-type cells and aggregation deficient mutants. J Biol Chem. 1986 Nov 15;261(32):15121–15125. [PubMed] [Google Scholar]
  44. Van Haastert P. J., De Vries M. J., Penning L. C., Roovers E., Van der Kaay J., Erneux C., Van Lookeren Campagne M. M. Chemoattractant and guanosine 5'-[gamma-thio]triphosphate induce the accumulation of inositol 1,4,5-trisphosphate in Dictyostelium cells that are labelled with [3H]inositol by electroporation. Biochem J. 1989 Mar 1;258(2):577–586. doi: 10.1042/bj2580577. [DOI] [PMC free article] [PubMed] [Google Scholar]
  45. Van Haastert P. J. Determination of inositol 1,4,5-trisphosphate levels in Dictyostelium by isotope dilution assay. Anal Biochem. 1989 Feb 15;177(1):115–119. doi: 10.1016/0003-2697(89)90024-9. [DOI] [PubMed] [Google Scholar]
  46. Van Haastert P. J. Guanine nucleotides modulate cell surface cAMP-binding sites in membranes from Dictyostelium discoideum. Biochem Biophys Res Commun. 1984 Oct 30;124(2):597–604. doi: 10.1016/0006-291x(84)91596-1. [DOI] [PubMed] [Google Scholar]
  47. Van Haastert P. J., Janssens P. M., Erneux C. Sensory transduction in eukaryotes. A comparison between Dictyostelium and vertebrate cells. Eur J Biochem. 1991 Jan 30;195(2):289–303. doi: 10.1111/j.1432-1033.1991.tb15706.x. [DOI] [PubMed] [Google Scholar]
  48. Van Haastert P. J., Kien E. Binding of cAMP derivatives to Dictyostelium discoideum cells. Activation mechanism of the cell surface cAMP receptor. J Biol Chem. 1983 Aug 25;258(16):9636–9642. [PubMed] [Google Scholar]
  49. Van Haastert P. J., Snaar-Jagalska B. E., Janssens P. M. The regulation of adenylate cyclase by guanine nucleotides in Dictyostelium discoideum membranes. Eur J Biochem. 1987 Jan 15;162(2):251–258. doi: 10.1111/j.1432-1033.1987.tb10592.x. [DOI] [PubMed] [Google Scholar]
  50. Van Haastert P. J. The modulation of cell surface cAMP receptors from Dictyostelium discoideum by ammonium sulfate. Biochim Biophys Acta. 1985 May 30;845(2):254–260. doi: 10.1016/0167-4889(85)90184-3. [DOI] [PubMed] [Google Scholar]
  51. Wessels D., Schroeder N. A., Voss E., Hall A. L., Condeelis J., Soll D. R. cAMP-mediated inhibition of intracellular particle movement and actin reorganization in Dictyostelium. J Cell Biol. 1989 Dec;109(6 Pt 1):2841–2851. doi: 10.1083/jcb.109.6.2841. [DOI] [PMC free article] [PubMed] [Google Scholar]
  52. Wu L. J., Devreotes P. N. Dictyostelium transiently expresses eight distinct G-protein alpha-subunits during its developmental program. Biochem Biophys Res Commun. 1991 Sep 30;179(3):1141–1147. doi: 10.1016/0006-291x(91)91690-e. [DOI] [PubMed] [Google Scholar]
  53. Yuen I. S., Gomer R. H. Cell density-sensing in Dictyostelium by means of the accumulation rate, diffusion coefficient and activity threshold of a protein secreted by starved cells. J Theor Biol. 1994 Apr 7;167(3):273–282. doi: 10.1006/jtbi.1994.1069. [DOI] [PubMed] [Google Scholar]
  54. Yuen I. S., Taphouse C., Halfant K. A., Gomer R. H. Regulation and processing of a secreted protein that mediates sensing of cell density in Dictyostelium. Development. 1991 Dec;113(4):1375–1385. doi: 10.1242/dev.113.4.1375. [DOI] [PubMed] [Google Scholar]

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