Abstract
Adhesion between Chlamydomonas reinhardtii gametes generates a rapid rise in cAMP levels which stimulates mating responses and zygotic cell fusion (Pasquale and Goodenough, 1987). We show here that sexual adhesion in vivo results in a twofold stimulation of flagellar adenylyl cyclase activity when the enzyme is subsequently assayed in vitro, a stimulation that is specifically blocked by Cd2+. A twofold stimulation is also elicited by the in vitro presentation of soluble cross-linking reagents (antisera and concanavalin A). In contrast, the 10-30-fold stimulation of the flagellar cyclase by in vitro exposure to 40 degrees C, first described by Zhang et al. (1991), is insensitive to Cd2+ but sensitive to such drugs as trifluoperizine and dibucaine. The capacity for twofold stimulation is displayed by the vegetative and gametic enzymes but is lost when gametes fuse to form zygotes; in contrast, the 10-fold stimulation is displayed by the gametic and zygotic enzymes but not the vegetative enzyme. The signal-defective mutant imp-3 fails to generate the normal mating-triggered cAMP production and can be rescued by exogenous dibutyryl cAMP. It displays normal basal rates of flagellar cyclase activity and a normal twofold stimulation by sexual adhesion and by soluble cross-linkers, but it is defective in 40 degrees C activation. The gametic cell-body adenylyl cyclase is stimulated when wild-type flagella, but not imp-3 flagella, undergo adhesive interactions in vivo, and it can be directly stimulated in vitro by cAMP presentation. We propose that the two levels of flagellar cyclase stimulation reflect either sequential steps in the activation of a single cyclase enzyme, with imp-3 blocked in the second step, or else the sequential activation of two different flagellar enzymes, with imp-3 defective in the second enzyme. We further propose that the cell- body enzyme is activated by the cAMP that is generated when flagellar cyclase activity is fully stimulated.
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Selected References
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- Adair W. S., Hwang C., Goodenough U. W. Identification and visualization of the sexual agglutinin from the mating-type plus flagellar membrane of Chlamydomonas. Cell. 1983 May;33(1):183–193. doi: 10.1016/0092-8674(83)90347-1. [DOI] [PubMed] [Google Scholar]
- Adair W. S., Jurivich D., Goodenough U. W. Localization of cellular antigens in sodium dodecyl sulfate-polyacrylamide gels. J Cell Biol. 1978 Oct;79(1):281–285. doi: 10.1083/jcb.79.1.281. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Adair W. S., Monk B. C., Cohen R., Hwang C., Goodenough U. W. Sexual agglutinins from the Chlamydomonas flagellar membrane. Partial purification and characterization. J Biol Chem. 1982 Apr 25;257(8):4593–4602. [PubMed] [Google Scholar]
- Bloodgood R. A. Calcium-regulated phosphorylation of proteins in the membrane-matrix compartment of the Chlamydomonas flagellum. Exp Cell Res. 1992 Feb;198(2):228–236. doi: 10.1016/0014-4827(92)90375-i. [DOI] [PubMed] [Google Scholar]
- Bloodgood R. A., Salomonsky N. L. Calcium influx regulates antibody-induced glycoprotein movements within the Chlamydomonas flagellar membrane. J Cell Sci. 1990 May;96(Pt 1):27–33. doi: 10.1242/jcs.96.1.27. [DOI] [PubMed] [Google Scholar]
- Bloodgood R. A., Salomonsky N. L. Regulation of flagellar glycoprotein movements by protein phosphorylation. Eur J Cell Biol. 1991 Feb;54(1):85–89. [PubMed] [Google Scholar]
- Collin-Osdoby P., Adair W. S. Characterization of the purified Chlamydomonas minus agglutinin. J Cell Biol. 1985 Sep;101(3):1144–1152. doi: 10.1083/jcb.101.3.1144. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Detmers P. A., Condeelis J. Trifluoperazine and W-7 inhibit mating in Chlamydomonas at an early stage of gametic interaction. Exp Cell Res. 1986 Apr;163(2):317–326. doi: 10.1016/0014-4827(86)90063-7. [DOI] [PubMed] [Google Scholar]
- Forest C. L., Goodenough D. A., Goodenough U. W. Flagellar membrane agglutination and sexual signaling in the conditional GAM-1 mutant of Chlamydomonas. J Cell Biol. 1978 Oct;79(1):74–84. doi: 10.1083/jcb.79.1.74. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Forest C. L., Togasaki R. K. Selection for conditional gametogenesis in Chlamydomonas reinhardi. Proc Natl Acad Sci U S A. 1975 Sep;72(9):3652–3655. doi: 10.1073/pnas.72.9.3652. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gilman A. G. G proteins and dual control of adenylate cyclase. Cell. 1984 Mar;36(3):577–579. doi: 10.1016/0092-8674(84)90336-2. [DOI] [PubMed] [Google Scholar]
- Gitelman S. E., Witman G. B. Purification of calmodulin from Chlamydomonas: calmodulin occurs in cell bodies and flagella. J Cell Biol. 1980 Dec;87(3 Pt 1):764–770. doi: 10.1083/jcb.87.3.764. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Goodenough U. W. Cyclic AMP enhances the sexual agglutinability of Chlamydomonas flagella. J Cell Biol. 1989 Jul;109(1):247–252. doi: 10.1083/jcb.109.1.247. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Goodenough U. W., Detmers P. A., Hwang C. Activation for cell fusion in Chlamydomonas: analysis of wild-type gametes and nonfusing mutants. J Cell Biol. 1982 Feb;92(2):378–386. doi: 10.1083/jcb.92.2.378. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Goodenough U. W. Experimental analysis of the adhesion reaction between isolated Chlamydomonas flagella. Exp Cell Res. 1986 Sep;166(1):237–246. doi: 10.1016/0014-4827(86)90523-9. [DOI] [PubMed] [Google Scholar]
- Goodenough U. W., Hwang C., Martin H. Isolation and genetic analysis of mutant strains of Chlamydomonas reinhardi defective in gametic differentiation. Genetics. 1976 Feb;82(2):169–186. doi: 10.1093/genetics/82.2.169. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Goodenough U. W., Jurivich D. Tipping and mating-structure activation induced in Chlamydomonas gametes by flagellar membrane antisera. J Cell Biol. 1978 Dec;79(3):680–693. doi: 10.1083/jcb.79.3.680. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Goodenough U. W., Shames B., Small L., Saito T., Crain R. C., Sanders M. A., Salisbury J. L. The role of calcium in the Chlamydomonas reinhardtii mating reaction. J Cell Biol. 1993 Apr;121(2):365–374. doi: 10.1083/jcb.121.2.365. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Goodenough U. W., StClair H. S. BALD-2: a mutation affecting the formation of doublet and triplet sets of microtubules in Chlamydomonas reinhardtii. J Cell Biol. 1975 Sep;66(3):480–491. doi: 10.1083/jcb.66.3.480. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Goodenough U. W. Tipping of flagellar agglutinins by gametes of Chlamydomonas reinhardtii. Cell Motil Cytoskeleton. 1993;25(2):179–189. doi: 10.1002/cm.970250207. [DOI] [PubMed] [Google Scholar]
- Gorman D. S., Levine R. P. Cytochrome f and plastocyanin: their sequence in the photosynthetic electron transport chain of Chlamydomonas reinhardi. Proc Natl Acad Sci U S A. 1965 Dec;54(6):1665–1669. doi: 10.1073/pnas.54.6.1665. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Huang B., Mengersen A., Lee V. D. Molecular cloning of cDNA for caltractin, a basal body-associated Ca2+-binding protein: homology in its protein sequence with calmodulin and the yeast CDC31 gene product. J Cell Biol. 1988 Jul;107(1):133–140. doi: 10.1083/jcb.107.1.133. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Huang B., Watterson D. M., Lee V. D., Schibler M. J. Purification and characterization of a basal body-associated Ca2+-binding protein. J Cell Biol. 1988 Jul;107(1):121–131. doi: 10.1083/jcb.107.1.121. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hunnicutt G. R., Kosfiszer M. G., Snell W. J. Cell body and flagellar agglutinins in Chlamydomonas reinhardtii: the cell body plasma membrane is a reservoir for agglutinins whose migration to the flagella is regulated by a functional barrier. J Cell Biol. 1990 Oct;111(4):1605–1616. doi: 10.1083/jcb.111.4.1605. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hunnicutt G. R., Snell W. J. Rapid and slow mechanisms for loss of cell adhesiveness during fertilization in Chlamydomonas. Dev Biol. 1991 Sep;147(1):216–224. doi: 10.1016/s0012-1606(05)80019-3. [DOI] [PubMed] [Google Scholar]
- Hwang C. J., Monk B. C., Goodenough U. W. Linkage of Mutations Affecting minus Flagellar Membrane Agglutinability to the mt Mating-Type Locus of Chlamydomonas. Genetics. 1981 Sep;99(1):41–47. doi: 10.1093/genetics/99.1.41. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kinoshita T., Fukuzawa H., Shimada T., Saito T., Matsuda Y. Primary structure and expression of a gamete lytic enzyme in Chlamydomonas reinhardtii: similarity of functional domains to matrix metalloproteases. Proc Natl Acad Sci U S A. 1992 May 15;89(10):4693–4697. doi: 10.1073/pnas.89.10.4693. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kooijman R., de Wildt P., Beumer S., van der Vliet G., Homan W., Kalshoven H., Musgrave A., van den Ende H. Wheat germ agglutinin induces mating reactions in Chlamydomonas eugametos by cross-linking agglutinin-associated glycoproteins in the flagellar membrane. J Cell Biol. 1989 Oct;109(4 Pt 1):1677–1687. doi: 10.1083/jcb.109.4.1677. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lansman J. B., Hess P., Tsien R. W. Blockade of current through single calcium channels by Cd2+, Mg2+, and Ca2+. Voltage and concentration dependence of calcium entry into the pore. J Gen Physiol. 1986 Sep;88(3):321–347. doi: 10.1085/jgp.88.3.321. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Martin N. C., Goodenough U. W. Gametic differentiation in Chlamydomonas reinhardtii. I. Production of gametes and their fine structure. J Cell Biol. 1975 Dec;67(3):587–605. doi: 10.1083/jcb.67.3.587. [DOI] [PMC free article] [PubMed] [Google Scholar]
- McLean R. J., Brown R. M. Cell surface differentiation of Chlamydomonas during gametogenesis. I. Mating and concanavalin A agglutinability. Dev Biol. 1974 Feb;36(2):279–285. doi: 10.1016/0012-1606(74)90051-7. [DOI] [PubMed] [Google Scholar]
- Mesland D. A., Hoffman J. L., Caligor E., Goodenough U. W. Flagellar tip activation stimulated by membrane adhesions in Chlamydomonas gametes. J Cell Biol. 1980 Mar;84(3):599–617. doi: 10.1083/jcb.84.3.599. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Millikin B. E., Weiss R. L. Distribution of concanavalin a binding carbohydrates during mating in Chlamydomonas. J Cell Sci. 1984 Mar;66:223–239. doi: 10.1242/jcs.66.1.223. [DOI] [PubMed] [Google Scholar]
- Mittal C. K. Determination of adenylate cyclase and guanylate cyclase activities in cells of the immune system. Methods Enzymol. 1986;132:422–428. doi: 10.1016/s0076-6879(86)32027-5. [DOI] [PubMed] [Google Scholar]
- Pasquale S. M., Goodenough U. W. Cyclic AMP functions as a primary sexual signal in gametes of Chlamydomonas reinhardtii. J Cell Biol. 1987 Nov;105(5):2279–2292. doi: 10.1083/jcb.105.5.2279. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Pfister K. K., Fay R. B., Witman G. B. Purification and polypeptide composition of dynein ATPases from Chlamydomonas flagella. Cell Motil. 1982;2(6):525–547. doi: 10.1002/cm.970020604. [DOI] [PubMed] [Google Scholar]
- Piperno G., Mead K., Shestak W. The inner dynein arms I2 interact with a "dynein regulatory complex" in Chlamydomonas flagella. J Cell Biol. 1992 Sep;118(6):1455–1463. doi: 10.1083/jcb.118.6.1455. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Salisbury J. L., Baron A. T., Sanders M. A. The centrin-based cytoskeleton of Chlamydomonas reinhardtii: distribution in interphase and mitotic cells. J Cell Biol. 1988 Aug;107(2):635–641. doi: 10.1083/jcb.107.2.635. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Salomon Y. Adenylate cyclase assay. Adv Cyclic Nucleotide Res. 1979;10:35–55. [PubMed] [Google Scholar]
- Snell W. J., Roseman S. Kinetics of adhesion and de-adhesion of Chlamydomonas gametes. J Biol Chem. 1979 Nov 10;254(21):10820–10829. [PubMed] [Google Scholar]
- Tang W. J., Gilman A. G. Adenylyl cyclases. Cell. 1992 Sep 18;70(6):869–872. doi: 10.1016/0092-8674(92)90236-6. [DOI] [PubMed] [Google Scholar]
- Ullrich A., Schlessinger J. Signal transduction by receptors with tyrosine kinase activity. Cell. 1990 Apr 20;61(2):203–212. doi: 10.1016/0092-8674(90)90801-k. [DOI] [PubMed] [Google Scholar]
- Witman G. B., Carlson K., Berliner J., Rosenbaum J. L. Chlamydomonas flagella. I. Isolation and electrophoretic analysis of microtubules, matrix, membranes, and mastigonemes. J Cell Biol. 1972 Sep;54(3):507–539. doi: 10.1083/jcb.54.3.507. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Zhang Y. H., Ross E. M., Snell W. J. ATP-dependent regulation of flagellar adenylylcyclase in gametes of Chlamydomonas reinhardtii. J Biol Chem. 1991 Dec 5;266(34):22954–22959. [PubMed] [Google Scholar]
- Zhang Y., Snell W. J. Differential regulation of adenylylcyclases in vegetative and gametic flagella of Chlamydomonas. J Biol Chem. 1993 Jan 25;268(3):1786–1791. [PubMed] [Google Scholar]