Effects of the central pair apparatus on microtubule sliding velocity in sea urchin sperm flagella.

To produce oscillatory bending movement in cilia and flagella, the activity of dynein arms must be regulated. The central-pair microtubules, located at the centre of the axoneme, are often thought to be involved in the regulation, but this has not been demonstrated definitively. In order to determine whether the central-pair apparatus are directly involved in the regulation of the dynein arm activity, we analyzed the movement of singlet microtubules that were brought into contact with dynein arms on bundles of doublets obtained by sliding disintegration of elastase-treated flagellar axonemes. An advantage of this new assay system was that we could distinguish the bundles that contained the central pair apparatus from those that did not, the former being clearly thicker than the latter. We found that microtubule sliding occurred along both the thinner and the thicker bundles, but its velocity differed between the two kinds of bundles in an ATP concentration dependent manner. At high ATP concentrations, such as 0.1 and 1 mM, the sliding velocity on the thinner bundles was significantly higher than that on the thicker bundles, while at lower ATP concentrations the sliding velocity did not change between the thinner and the thicker bundles. We observed similar bundle width-related differences in sliding velocity after removal of the outer arms. These results provide first evidence suggesting that the central pair and its associated structures may directly regulate the activity of the inner (and probably also the outer) arm dynein.

[1]  J. Rossier,et al.  Tubulin polyglycylation: differential posttranslational modification of dynamic cytoplasmic and stable axonemal microtubules in paramecium. , 1998, Molecular biology of the cell.

[2]  Toshio Yanagida,et al.  Dynein arms are oscillating force generators , 1998, Nature.

[3]  K. Johnson,et al.  The axonemal microtubules of the Chlamydomonas flagellum differ in tubulin isoform content. , 1998, Journal of cell science.

[4]  W. Sale,et al.  Regulation of Flagellar Dynein by Phosphorylation of a 138-kD Inner Arm Dynein Intermediate Chain , 1997, The Journal of cell biology.

[5]  U. Plessmann,et al.  The A and B tubules of the outer doublets of sea urchin sperm axonemes are composed of different tubulin variants. , 1996, Biochemistry.

[6]  W. Sale,et al.  Regulation of flagellar dynein by an axonemal type-1 phosphatase in Chlamydomonas. , 1996, Journal of cell science.

[7]  J. Rossier,et al.  Axonemal tubulin polyglycylation probed with two monoclonal antibodies: widespread evolutionary distribution, appearance during spermatozoan maturation and possible function in motility. , 1996, Journal of cell science.

[8]  C. Shingyoji,et al.  Cyclical bending movements induced locally by successive iontophoretic application of ATP to an elastase-treated flagellar axoneme. , 1995, Journal of cell science.

[9]  I. Gibbons,et al.  Effect of beat frequency on the velocity of microtubule sliding in reactivated sea urchin sperm flagella under imposed head vibration. , 1995, The Journal of experimental biology.

[10]  W. Sale,et al.  Regulation of Chlamydomonas flagellar dynein by an axonemal protein kinase , 1994, The Journal of cell biology.

[11]  S. Dutcher,et al.  Mutations in the SUP-PF-1 locus of Chlamydomonas reinhardtii identify a regulatory domain in the beta-dynein heavy chain , 1994, The Journal of cell biology.

[12]  G. Piperno,et al.  Mutations in the "dynein regulatory complex" alter the ATP-insensitive binding sites for inner arm dyneins in Chlamydomonas axonemes , 1994, The Journal of cell biology.

[13]  F. Pinardi,et al.  Cytolocation of prosome antigens on intermediate filament subnetworks of cytokeratin, vimentin and desmin type. , 1994, Journal of cell science.

[14]  I. Mabuchi,et al.  Isolation and characterization of a novel dynein that contains C and A heavy chains from sea urchin sperm flagellar axonemes. , 1994, Journal of cell science.

[15]  T. Miki-Noumura,et al.  Inhibition of gliding movement by calcium in doublet microtubules on Tetrahymena ciliary dyneins in vitro. , 1992, Experimental cell research.

[16]  R. Kamiya,et al.  Translocation and rotation of microtubules caused by multiple species of Chlamydomonas inner-arm dynein , 1992 .

[17]  W. Sale,et al.  Regulation of dynein-driven microtubule sliding by the radial spokes in flagella. , 1992, Science.

[18]  G. Piperno,et al.  The inner dynein arms I2 interact with a "dynein regulatory complex" in Chlamydomonas flagella , 1992, The Journal of cell biology.

[19]  S. Dutcher,et al.  Extragenic suppressors of paralyzed flagellar mutations in Chlamydomonas reinhardtii identify loci that alter the inner dynein arms , 1992, The Journal of cell biology.

[20]  J. Gatti,et al.  The motile beta/IC1 subunit of sea urchin sperm outer arm dynein does not form a rigor bond , 1992, The Journal of cell biology.

[21]  R. Vale,et al.  Nucleotide specificity of the enzymatic and motile activities of dynein, kinesin, and heavy meromyosin , 1991, The Journal of cell biology.

[22]  I. Gibbons,et al.  Rotating the plane of imposed vibration can rotate the plane of flagellar beating in sea-urchin sperm without twisting the axoneme. , 1991, Journal of cell science.

[23]  R. Vale,et al.  One-dimensional diffusion of microtubules bound to flagellar dynein , 1989, Cell.

[24]  R. Vale,et al.  Microtubule translocation properties of intact and proteolytically digested dyneins from Tetrahymena cilia , 1989, The Journal of cell biology.

[25]  W. Sale,et al.  Isolated beta-heavy chain subunit of dynein translocates microtubules in vitro , 1988, The Journal of cell biology.

[26]  T. Miki-Noumura,et al.  Bending motion of Chlamydomonas axonemes after extrusion of central- pair microtubules , 1987, The Journal of cell biology.

[27]  I. Gibbons,et al.  Spontaneous recovery after experimental manipulation of the plane of beat in sperm flagella , 1987, Nature.

[28]  W. Sale The axonemal axis and Ca2+-induced asymmetry of active microtubule sliding in sea urchin sperm tails , 1986, The Journal of cell biology.

[29]  K. Ishiguro,et al.  Phosphoprotein phosphatase inhibits flagellar movement of Triton models of sea urchin spermatozoa. , 1985, Cell structure and function.

[30]  K. Ishiguro,et al.  Evidence that cAMP-dependent protein kinase and a protein factor are involved in reactivation of triton X-100 models of sea urchin and starfish spermatozoa , 1982, The Journal of cell biology.

[31]  S. Dutcher,et al.  Analysis of the movement of Chlamydomonas flagella:" the function of the radial-spoke system is revealed by comparison of wild-type and mutant flagella , 1982, The Journal of cell biology.

[32]  D. Luck,et al.  Suppressor mutations in chlamydomonas reveal a regulatory mechanism for flagellar function , 1982, Cell.

[33]  G. Witman,et al.  Functionally significant central-pair rotation in a primitive eukaryotic flagellum , 1981, Nature.

[34]  T. Miki-Noumura,et al.  Recovery of sliding ability in arm-depleted flagellar axonemes after recombination with extracted dynein I. , 1981, Journal of cell science.

[35]  C. Kung,et al.  Rotation and twist of the central-pair microtubules in the cilia of Paramecium , 1980, The Journal of cell biology.

[36]  C. Kung,et al.  The pair of central tubules rotates during ciliary beat in Paramecium , 1979, Nature.

[37]  G. Witman,et al.  Chlamydomonas flagellar mutants lacking radial spokes and central tubules. Structure, composition, and function of specific axonemal components , 1978, The Journal of cell biology.

[38]  I. Gibbons,et al.  The Effect of Partial Extraction of Dynein Arms on the Movement of Reactivated Sea-urchin Sperm , 2022 .

[39]  I. Gibbons,et al.  Adenosine triphosphate-induced sliding of tubules in trypsin-treated flagella of sea-urchin sperm. , 1971, Proceedings of the National Academy of Sciences of the United States of America.

[40]  G. Horridge,et al.  The relation between the orientation of the central fibrils and the direction of beat in cilia of Opalina , 1970, Proceedings of the Royal Society of London. Series B. Biological Sciences.

[41]  I. Gibbons THE RELATIONSHIP BETWEEN THE FINE STRUCTURE AND DIRECTION OF BEAT IN GILL CILIA OF A LAMELLIBRANCH MOLLUSC , 1961, The Journal of biophysical and biochemical cytology.

[42]  H. Sakakibara,et al.  Unidirectional movement of fluorescent microtubules on rows of dynein arms of disintegrated axonemes. , 1998, Journal of cell science.

[43]  E. Kurimoto,et al.  Ability of paralyzed flagella mutants of Chlamydomonas to move. , 1996, Cell motility and the cytoskeleton.

[44]  W. Sale,et al.  Regulation of dynein-driven microtubule sliding by an axonemal kinase and phosphatase in Chlamydomonas flagella. , 1995, Cell motility and the cytoskeleton.

[45]  E. Kurimoto,et al.  Microtubule sliding in flagellar axonemes of Chlamydomonas mutants missing inner- or outer-arm dynein: velocity measurements on new types of mutants by an improved method. , 1991, Cell motility and the cytoskeleton.

[46]  W. Sale,et al.  Microtubule binding and translocation by inner dynein arm subtype I1. , 1991, Cell motility and the cytoskeleton.

[47]  P. Satir,et al.  Splitting the ciliary axoneme: implications for a "switch-point" model of dynein arm activity in ciliary motion. , 1989, Cell motility and the cytoskeleton.

[48]  T. Miki-Noumura,et al.  Stepwise sliding disintegration of Tetrahymena ciliary axonemes at higher concentrations of ATP , 1988 .

[49]  S. Asakura,et al.  Stimulation of in vitro motility of Chlamydomonas axonemes by inhibition of cAMP-dependent phosphorylation. , 1987, Cell motility and the cytoskeleton.

[50]  K. Ishiguro,et al.  Regulation of sperm flagellar movement by protein phosphorylation and dephosphorylation. , 1986, Cell motility and the cytoskeleton.

[51]  C. Brokaw,et al.  Bending patterns of chlamydomonas flagella: III. A radial spoke head deficient mutant and a central pair deficient mutant. , 1985, Cell motility.

[52]  I. Gibbons,et al.  Live and reactivated motility in the 9+0 flagellum of Anguilla sperm. , 1985, Cell motility.

[53]  R. Kamiya Extrusion and Rotation of the central-pair microtubules in detergent-treated Chlamydomonas flagella. , 1982, Progress in clinical and biological research.

[54]  C. Brokaw,et al.  Calcium‐induced change in form of demembranated sea urchin sperm flagella immobilized by vanadate , 1981 .