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. 1993 Oct 1;123(1):183–190. doi: 10.1083/jcb.123.1.183

Assembly of flagellar radial spoke proteins in Chlamydomonas: identification of the axoneme binding domain of radial spoke protein 3

PMCID: PMC2119812  PMID: 8408197

Abstract

Radial spokes of the eukaryotic flagellum extend from the A tubule of each outer doublet microtubule toward the central pair microtubules. In the paralyzed flagella mutant of Chlamydomonas pf14, a mutation in the gene for one of 17 polypeptides that comprise the radial spokes results in flagella that lack all 17 spoke components. The defective gene product, radial spoke protein 3 (RSP3), is, therefore, pivotal to the assembly of the entire spoke and may attach the spoke to the axoneme. We have synthesized RSP3 in vitro and assayed its binding to axonemes from pf14 cells to determine if RSP3 can attach to spokeless axonemes. In vitro, RSP3 binds to pf14 axonemes, but not to wild-type axonemes or microtubules polymerized from purified chick brain tubulin. The sole axoneme binding domain of RSP3 is located within amino acids 1-85 of the 516 amino acid protein; deletion of these amino acids abolishes binding by RSP3. Fusion of amino acids 1-85 or 42-85 to an unrelated protein confers complete or partial binding activity, respectively, to the fusion protein. Transformation of pf14 cells with mutagenized RSP3 genes indicates that amino acids 18-87 of RSP3 are important to its function, but that the carboxy-terminal 140 amino acids can be deleted with little effect on radial spoke assembly or flagellar motility.

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Selected References

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  1. Bloom G. S. Motor proteins for cytoplasmic microtubules. Curr Opin Cell Biol. 1992 Feb;4(1):66–73. doi: 10.1016/0955-0674(92)90060-p. [DOI] [PubMed] [Google Scholar]
  2. Brokaw C. J., Luck D. J., Huang B. Analysis of the movement of Chlamydomonas flagella:" the function of the radial-spoke system is revealed by comparison of wild-type and mutant flagella. J Cell Biol. 1982 Mar;92(3):722–732. doi: 10.1083/jcb.92.3.722. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Chapin S. J., Bulinski J. C. Microtubule stabilization by assembly-promoting microtubule-associated proteins: a repeat performance. Cell Motil Cytoskeleton. 1992;23(4):236–243. doi: 10.1002/cm.970230403. [DOI] [PubMed] [Google Scholar]
  4. Curry A. M., Rosenbaum J. L. Flagellar radial spoke: a model molecular genetic system for studying organelle assembly. Cell Motil Cytoskeleton. 1993;24(4):224–232. doi: 10.1002/cm.970240403. [DOI] [PubMed] [Google Scholar]
  5. Curry A. M., Williams B. D., Rosenbaum J. L. Sequence analysis reveals homology between two proteins of the flagellar radial spoke. Mol Cell Biol. 1992 Sep;12(9):3967–3977. doi: 10.1128/mcb.12.9.3967. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Diener D. R., Curry A. M., Johnson K. A., Williams B. D., Lefebvre P. A., Kindle K. L., Rosenbaum J. L. Rescue of a paralyzed-flagella mutant of Chlamydomonas by transformation. Proc Natl Acad Sci U S A. 1990 Aug;87(15):5739–5743. doi: 10.1073/pnas.87.15.5739. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Ernst H., Duncan R. F., Hershey J. W. Cloning and sequencing of complementary DNAs encoding the alpha-subunit of translational initiation factor eIF-2. Characterization of the protein and its messenger RNA. J Biol Chem. 1987 Jan 25;262(3):1206–1212. [PubMed] [Google Scholar]
  8. Fernández E., Schnell R., Ranum L. P., Hussey S. C., Silflow C. D., Lefebvre P. A. Isolation and characterization of the nitrate reductase structural gene of Chlamydomonas reinhardtii. Proc Natl Acad Sci U S A. 1989 Sep;86(17):6449–6453. doi: 10.1073/pnas.86.17.6449. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Field J., Nikawa J., Broek D., MacDonald B., Rodgers L., Wilson I. A., Lerner R. A., Wigler M. Purification of a RAS-responsive adenylyl cyclase complex from Saccharomyces cerevisiae by use of an epitope addition method. Mol Cell Biol. 1988 May;8(5):2159–2165. doi: 10.1128/mcb.8.5.2159. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Goodenough U. W., Heuser J. E. Substructure of inner dynein arms, radial spokes, and the central pair/projection complex of cilia and flagella. J Cell Biol. 1985 Jun;100(6):2008–2018. doi: 10.1083/jcb.100.6.2008. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Haimo L. T., Telzer B. R., Rosenbaum J. L. Dynein binds to and crossbridges cytoplasmic microtubules. Proc Natl Acad Sci U S A. 1979 Nov;76(11):5759–5763. doi: 10.1073/pnas.76.11.5759. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Hopkins J. M. Subsidiary components of the flagella of Chlamydomonas reinhardii. J Cell Sci. 1970 Nov;7(3):823–839. doi: 10.1242/jcs.7.3.823. [DOI] [PubMed] [Google Scholar]
  13. Huang B., Ramanis Z., Luck D. J. Suppressor mutations in Chlamydomonas reveal a regulatory mechanism for Flagellar function. Cell. 1982 Jan;28(1):115–124. doi: 10.1016/0092-8674(82)90381-6. [DOI] [PubMed] [Google Scholar]
  14. Johnson K. A., Rosenbaum J. L. Flagellar regeneration in Chlamydomonas: a model system for studying organelle assembly. Trends Cell Biol. 1993 May;3(5):156–161. doi: 10.1016/0962-8924(93)90136-o. [DOI] [PubMed] [Google Scholar]
  15. Johnson K. A., Rosenbaum J. L. Polarity of flagellar assembly in Chlamydomonas. J Cell Biol. 1992 Dec;119(6):1605–1611. doi: 10.1083/jcb.119.6.1605. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Kindle K. L. High-frequency nuclear transformation of Chlamydomonas reinhardtii. Proc Natl Acad Sci U S A. 1990 Feb;87(3):1228–1232. doi: 10.1073/pnas.87.3.1228. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Kindle K. L., Schnell R. A., Fernández E., Lefebvre P. A. Stable nuclear transformation of Chlamydomonas using the Chlamydomonas gene for nitrate reductase. J Cell Biol. 1989 Dec;109(6 Pt 1):2589–2601. doi: 10.1083/jcb.109.6.2589. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. King S. M., Wilkerson C. G., Witman G. B. The Mr 78,000 intermediate chain of Chlamydomonas outer arm dynein interacts with alpha-tubulin in situ. J Biol Chem. 1991 May 5;266(13):8401–8407. [PubMed] [Google Scholar]
  19. Kozminski K. G., Diener D. R., Rosenbaum J. L. High level expression of nonacetylatable alpha-tubulin in Chlamydomonas reinhardtii. Cell Motil Cytoskeleton. 1993;25(2):158–170. doi: 10.1002/cm.970250205. [DOI] [PubMed] [Google Scholar]
  20. L'Hernault S. W., Rosenbaum J. L. Chlamydomonas alpha-tubulin is posttranslationally modified in the flagella during flagellar assembly. J Cell Biol. 1983 Jul;97(1):258–263. doi: 10.1083/jcb.97.1.258. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Laemmli U. K. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature. 1970 Aug 15;227(5259):680–685. doi: 10.1038/227680a0. [DOI] [PubMed] [Google Scholar]
  22. Lefebvre P. A., Rosenbaum J. L. Regulation of the synthesis and assembly of ciliary and flagellar proteins during regeneration. Annu Rev Cell Biol. 1986;2:517–546. doi: 10.1146/annurev.cb.02.110186.002505. [DOI] [PubMed] [Google Scholar]
  23. Luck D., Piperno G., Ramanis Z., Huang B. Flagellar mutants of Chlamydomonas: studies of radial spoke-defective strains by dikaryon and revertant analysis. Proc Natl Acad Sci U S A. 1977 Aug;74(8):3456–3460. doi: 10.1073/pnas.74.8.3456. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Mastronarde D. N., O'Toole E. T., McDonald K. L., McIntosh J. R., Porter M. E. Arrangement of inner dynein arms in wild-type and mutant flagella of Chlamydomonas. J Cell Biol. 1992 Sep;118(5):1145–1162. doi: 10.1083/jcb.118.5.1145. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Mitchell D. R., Kang Y. Identification of oda6 as a Chlamydomonas dynein mutant by rescue with the wild-type gene. J Cell Biol. 1991 May;113(4):835–842. doi: 10.1083/jcb.113.4.835. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Pelham H. R., Jackson R. J. An efficient mRNA-dependent translation system from reticulocyte lysates. Eur J Biochem. 1976 Aug 1;67(1):247–256. doi: 10.1111/j.1432-1033.1976.tb10656.x. [DOI] [PubMed] [Google Scholar]
  27. Piperno G., Huang B., Ramanis Z., Luck D. J. Radial spokes of Chlamydomonas flagella: polypeptide composition and phosphorylation of stalk components. J Cell Biol. 1981 Jan;88(1):73–79. doi: 10.1083/jcb.88.1.73. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. 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]
  29. Rosenbaum J. L., Child F. M. Flagellar regeneration in protozoan flagellates. J Cell Biol. 1967 Jul;34(1):345–364. doi: 10.1083/jcb.34.1.345. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Segal R. A., Luck D. J. Phosphorylation in isolated Chlamydomonas axonemes: a phosphoprotein may mediate the Ca2+-dependent photophobic response. J Cell Biol. 1985 Nov;101(5 Pt 1):1702–1712. doi: 10.1083/jcb.101.5.1702. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. Silflow C. D., Chisholm R. L., Conner T. W., Ranum L. P. The two alpha-tubulin genes of Chlamydomonas reinhardi code for slightly different proteins. Mol Cell Biol. 1985 Sep;5(9):2389–2398. doi: 10.1128/mcb.5.9.2389. [DOI] [PMC free article] [PubMed] [Google Scholar]
  32. Sloboda R. D., Rosenbaum J. L. Purification and assay of microtubule-associated proteins (MAPs). Methods Enzymol. 1982;85(Pt B):409–416. doi: 10.1016/0076-6879(82)85041-6. [DOI] [PubMed] [Google Scholar]
  33. Smith E. F., Sale W. S. Regulation of dynein-driven microtubule sliding by the radial spokes in flagella. Science. 1992 Sep 11;257(5076):1557–1559. doi: 10.1126/science.1387971. [DOI] [PubMed] [Google Scholar]
  34. Smith E. F., Sale W. S. Structural and functional reconstitution of inner dynein arms in Chlamydomonas flagellar axonemes. J Cell Biol. 1992 May;117(3):573–581. doi: 10.1083/jcb.117.3.573. [DOI] [PMC free article] [PubMed] [Google Scholar]
  35. Snell W. J., Dentler W. L., Haimo L. T., Binder L. I., Rosenbaum J. L. Assembly of chick brain tubulin onto isolated basal bodies of Chlamydomonas reinhardi. Science. 1974 Jul 26;185(4148):357–360. doi: 10.1126/science.185.4148.357. [DOI] [PubMed] [Google Scholar]
  36. Warner F. D. New observations on flagellar fine structure. The relationship between matrix structure and the microtubule component of the axoneme. J Cell Biol. 1970 Oct;47(1):159–182. doi: 10.1083/jcb.47.1.159. [DOI] [PMC free article] [PubMed] [Google Scholar]
  37. Warner F. D., Satir P. The structural basis of ciliary bend formation. Radial spoke positional changes accompanying microtubule sliding. J Cell Biol. 1974 Oct;63(1):35–63. doi: 10.1083/jcb.63.1.35. [DOI] [PMC free article] [PubMed] [Google Scholar]
  38. Williams B. D., Mitchell D. R., Rosenbaum J. L. Molecular cloning and expression of flagellar radial spoke and dynein genes of Chlamydomonas. J Cell Biol. 1986 Jul;103(1):1–11. doi: 10.1083/jcb.103.1.1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  39. Williams B. D., Velleca M. A., Curry A. M., Rosenbaum J. L. Molecular cloning and sequence analysis of the Chlamydomonas gene coding for radial spoke protein 3: flagellar mutation pf-14 is an ochre allele. J Cell Biol. 1989 Jul;109(1):235–245. doi: 10.1083/jcb.109.1.235. [DOI] [PMC free article] [PubMed] [Google Scholar]
  40. Witman G. B. Axonemal dyneins. Curr Opin Cell Biol. 1992 Feb;4(1):74–79. doi: 10.1016/0955-0674(92)90061-g. [DOI] [PubMed] [Google Scholar]
  41. 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]
  42. Witman G. B., Plummer J., Sander G. Chlamydomonas flagellar mutants lacking radial spokes and central tubules. Structure, composition, and function of specific axonemal components. J Cell Biol. 1978 Mar;76(3):729–747. doi: 10.1083/jcb.76.3.729. [DOI] [PMC free article] [PubMed] [Google Scholar]
  43. Witman G. B. The site of in vivo assembly of flagellar microtubules. Ann N Y Acad Sci. 1975 Jun 30;253:178–191. doi: 10.1111/j.1749-6632.1975.tb19199.x. [DOI] [PubMed] [Google Scholar]
  44. Youngblom J., Schloss J. A., Silflow C. D. The two beta-tubulin genes of Chlamydomonas reinhardtii code for identical proteins. Mol Cell Biol. 1984 Dec;4(12):2686–2696. doi: 10.1128/mcb.4.12.2686. [DOI] [PMC free article] [PubMed] [Google Scholar]

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