Skip to main content
Log in

Cytology of lepidoptera VIII. Acetylation of α-tubulin in mitotic and meiotic spindles of two Lepidoptera species,Ephestia kuehniella (Pyralidae) andPieris brassicae (Pieridae)

  • Published:
Protoplasma Aims and scope Submit manuscript

Summary

The microtubular spindle in spermatocytes of Lepidoptera is unconventional in that the bulk of the microtubules (MTs) ends relatively abrupt about halfway between the spindle equator and the centrosomes from late prometaphase through early anaphase. Membranous elements separate the MT ends from the centrosomes. In the present study, the question is addressed whether MTs in meiotic spindles of male Lepidoptera are — as typical of spindle MTs in other systems — highly dynamic or whether they represent a more stable MT population. To this end, primary spermatocytes of two Lepidoptera species,Ephestia kuehniella (Pyralidae) andPieris brassicae (Pieridae), were probed with a widely used antibody, 6–11B-1, directed against acetylated α-tubulin. Tubulin acetylation is believed to indicate the presence of long-lived MTs. In late telophase spermatocytes of both species, spindle MTs were highly acetylated. This is in keeping with observations in other systems: MT dynamics decreases towards telophase. The labeling intensity in younger spermatocytes differed, however, between both species. InE. kuehniella only flagella were labeled, whereas inP. brassicae also the kinetochore MTs and small MT arrays around the centrosomes were detected by the antibody against acetylated α-tubullin. The findings are compatible with the suggestion that spindle MTs are dynamic in prometaphase to anaphase spermatocytes ofE. kuehniella. In fact, treatment with taxol, a MT-stabilizing drug, leads to high acetylation of α-tubulin throughout spindle MTs ofE. kuehniella in this period. Meiotic spindles inP. brassicae are longer by a factor of 1.3 than those ofE. kuehniella. The shorter MTs inE. kuehniella may turnover completely and cannot accumulate acetylated portions, whereas segments of MTs in the longer spindles ofP. brassicae persist and become post-translationally acetylated. Spermatogonial mitosis was also studied in both species and spindle MTs were found highly acetylated throughout mitosis. Thus, mitotic and meiotic spindles in males of Lepidoptera differ with respect to MT turnover.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

Abbreviations

BSA:

bovine serum albumin

DAPI:

4′,6-Diamidino-2-phenylindole-2 HC1

EGTA:

ethylene glycol-bis (β-aminoethyl ether)-N,N′-tetraacetic acid

PBS:

phosphate-buffered saline

PIPES:

piperazine-N,N′-bis (2-ethane sulfonic acid)

MT:

microtubule

References

  • Baum SC, Wittner M, Nadler JP, Horwitz SB, Dennis JE, Schiff PB, Tanowitz HB (1981) Taxol, a microtubule stabilizing agent, blocks the replication ofTrypanosoma cruzi. Proc Natl Acad Sci USA 78: 4571–4575

    Google Scholar 

  • Cambray-Deakin MA, Burgoyne RD (1987) Acetylated and detyrosinated α-tubulin are co-localized in stable microtubules in rat meningeal fibroblasts. Cell Motil Cytoskeleton 8: 284–291

    Google Scholar 

  • Bigger TRL (1975) Karyotypes of some Lepidoptera chromosomes and changes in their holokinetic organisation as revealed by new cytological techniques. Cytologia 40: 713–726

    Google Scholar 

  • Bulinski JC, Richards JE, Piperno G (1988) Post-translational modifications of α-tubulin. Detyrosination and acetylation differentiate populations of interphase microtubules in cultured cells. J Cell Biol 106: 1213–1220

    Google Scholar 

  • de Pennart H, Houliston E, Maro B (1988) Post-translational modifications of tubulin and the dynamics of microtubules in mouse oocytes and zygotes. Biol Cell 64: 375–378

    Google Scholar 

  • Diggins MA, Dove WE (1987) Distribution of acetylated α-tubulin inPhysarum polycephalum. J Cell Biol 104: 303–309

    Google Scholar 

  • Gelfand VI, Bershadsky AD (1991) Microtubule dynamics: mechanism, regulation, and function. Annu Rev Cell Biol 7: 93–116

    Google Scholar 

  • Gundersen GG, Khawaja S, Bulinski C (1989) Generation of a stable, post-translationally modified microtubule array is an early event in myogenic differentiation. J Cell Biol 109: 2275–2288

    Google Scholar 

  • Hamaguchi Y, Toriyama M, Sakai H, Hiramoto Y (1985) Distribution of fluorescently labeled tubulin injected into sand dollar eggs from fertilization through cleavage. J Cell Biol 100: 1262–1272

    Google Scholar 

  • Harrison A, Stebbings H, Hyams JS (1991) Different patterns of α-tubulin post-translational modification in ovarian tubes of two hemipteran insects. J Cell Sci 100: 501–507

    Google Scholar 

  • Hermo L, Oko R, Hecht NB (1991) Differential post-translational modifications of microtubules in cells of the seminiferous epithelium of the rat: a light and electron microscopy immunocytochemical study. Anat Rec 229: 31–50

    Google Scholar 

  • Holy TE, Leibler S (1994) Dynamic instability of microtubules as an efficient way to search in space. Proc Natl Acad Sei USA 91: 5682–5685

    Google Scholar 

  • Jasmin BJ, Changera J-P, Cartaud J (1990) Compartmentalization of cold-stable and acetylated microtubules in the subsynaptic domain of chick skeletal muscle fibre. Nature 344: 673–675

    Google Scholar 

  • Joshi H (1994) Microtubule organizing centers and gamma-tubulin. Curr Opin Cell Biol 6: 55–62

    Google Scholar 

  • LeDizet M, Piperno G (1986) Cytoplasmic microtubules containing acetylated α-tubulin inChlamydomonas reinhardtii: spatial arrangement and properties. J Cell Biol 103: 13–22

    Google Scholar 

  • MacRae TH, Langdon CM, Freeman JA (1991) Spatial distribution of post-translationally modified tubulins in polarized cells of developingArtemia. Cell Motil Cytoskeleton 18: 189–203

    Google Scholar 

  • Mandelkow E-M, Mandelkow E, Milligan RA (1991) Microtubule dynamics and microtubule caps: a time-resolved cryo-electron microscopy study. J Cell Biol 114: 977–991

    Google Scholar 

  • Manfredi JJ, Fant J, Horwitz SB (1986) Taxol induces the formation of unusual arrays of cellular microtubules in colchicine-pretreated J774.2 cells. Eur J Cell Biol 42: 126–134

    Google Scholar 

  • Mazia D (1984) Centrosomes and mitotic ploles. Exp Cell Res 153: 1–15

    Google Scholar 

  • McBeath E, Fujiwara K (1990) Microtubule detachment from the microtubule-organizing center as a key event in the complete turnover of microtubules in cells. Eur J Cell Biol 52: 1–16

    Google Scholar 

  • Melan MA (1990) Taxol maintains organized microtubule patterns in protoplasts which lead to the resynthesis of organized cell wall microfibrils. Protoplasma 153: 169–177

    Google Scholar 

  • Nicklas RB (1988) Chance encounters and precision in mitosis. J Cell Sci 89: 87–104

    Google Scholar 

  • Osanai M, Kasuga H, Aigaki T (1987) Physiological role of apyrene spermatozoa ofBombyx mori. Experientia 43: 593–596

    Google Scholar 

  • Osborn M, Weber K (1982) Immunofluorescence and immunocytochemical procedures with affinity purified antibodies: tubulin containing structures. Methods Cell Biol 24: 97–132

    Google Scholar 

  • Piperno G, Fuller MT (1985) Monoclonal antibodies specific for an acetylated form of α-tubulin recognize the antigen in cilia and flagella from a variety of organisms. J Cell Biol 101: 2085–2094

    Google Scholar 

  • —, EeDizet M, Chang X (1987) Microtubules containing acetylated α-tubulin in mammalian cells in culture. J Cell Biol 104: 289–302

    Google Scholar 

  • Sasse R, Gull K (1988) Tubulin post-translational modifications and the construction of microtubular organelles inTrypanosoma brucei. J Cell Sci 90: 577–589

    Google Scholar 

  • Saxton WM, Stemple DL, Leslie RJ, Salmon ED, Zavortink M, McIntosh JR (1984) Tubulin dynamics in cultured mammalian cells. J Cell Biol 99: 2175–2186

    Google Scholar 

  • Schatten G, Simerly C, Asai DJ, Szöke E, Cooke P, Schatten H (1988) Acetylated α-tubulin in microtubules during mouse fertilization and early development. Dev Biol 130: 74–86

    Google Scholar 

  • Schiff PB, Horwitz SB (1980) Taxol stabilizes microtubules in mouse fibroblast cells. Proc Natl Acad Sci USA 77: 1561–1565

    Google Scholar 

  • — — (1981) Taxol assembles tubulin in the absence of exogenous 5′-triphosphate or microtubule-associated proteins. Biochemistry 20: 3247–3252

    Google Scholar 

  • —, Fant J, Horwitz SB (1979) Promotion of microtubule assembly in vitro by taxol. Nature 277: 665–667

    Google Scholar 

  • Shelden E, Wadsworth P (1990) Interzonal microtubules are dynamic during spindle elongation. J Cell Sci 97: 273–281

    Google Scholar 

  • — — (1993) Observation and quantification of individual microtubule behavior in vivo: microtubule dynamics are cell-type specific. J Cell Biol 120: 935–945

    Google Scholar 

  • Silberglied RT, Sheperd JG, Dickinson JL (1984) Eunuchs: the role of the apyrene sperm in Lepidoptera? Am Nat 123: 255–265

    Google Scholar 

  • Takemura R, Okabe S, Umeyama T, Kanal Y, Cowan N, Hirokawa N (1992) Increased microtubule-stability and alpha tubulin acetylation in cells transfected with microtubule-associated proteins MAP1B, MAP2 or tau. J Cell Sci 103, 953–964

    Google Scholar 

  • Traut W, Mosbacher GC (1968) Geschlechtschromatin bei Lepidopteren. Chromosoma 25: 343–356

    Google Scholar 

  • —, Weith A, Traut G (1986) Structural mutants of the W chromosome inEphestia (Insecta, Lepidoptera). Genetica 70: 69–79

    Google Scholar 

  • Wadsworth P, McGrail M (1990) Interphase microtubule dynamics are cell type-specific. J Cell Sci 95: 23–32

    Google Scholar 

  • Webster DL, Borisy GG (1989) Microtubules are acetylated in domains that turnover slowly. J Cell Sci 92: 57–65

    Google Scholar 

  • Wilson PJ, Forer A (1989) Acetylated α-tubulin in spermatogenic cells of the crane flyNephrotoma suturalis: kinetochore microtubules are selectively acetylated. Cell Motil Cytoskeleton 14: 237–250

    Google Scholar 

  • — —, Laggiadro C (1994) Evidence that kinetochore microtubules in crane-fly spermatocytes disassemble during anaphase primarily at the poleward end. J Cell Sci 107: 3015–3027

    Google Scholar 

  • Wolf KW (1990a) Sheathed nuclear division in primary spermatocytes ofOrgyia antiqua (Lepidoptera, Insecta). BioSystems 24: 5–15

    Google Scholar 

  • — (1990b) Mitotic and meiotic spindles from two insect orders, Lepidoptera and Diptera, differ in terms of microtubule and membrane content. J Cell Sci 97: 91–100

    Google Scholar 

  • — (1992) Spindle membranes and microtubules are coordinately reduced in apyrene relative to eupyrene spermatocytes ofInachisio (Lepidoptera, Nymphalidae). J Submicrosc Cytol Pathol 24: 381–394

    Google Scholar 

  • — (1994) The unique structure of Lepidopteran spindles. Int Rev Cytol 152: 1–48

    Google Scholar 

  • — (1995) Spindle membranes and spindle architecture in invertebrates. Micron 26: 69–98

    Google Scholar 

  • —, Bastmeyer M (1991a) Cytology of Lepidoptera. V. The microtubule cytoskeleton in eupyrene spermatocytes ofEphestia kuehniella (Pyralidae),Inachis io (Nymphalidae), andOrgyia antiqua (Lymantriidae). Eur J Cell Biol 55: 225–237

    Google Scholar 

  • — (1991b) Cytology of Lepidoptera. VI. Immunolocalization of microtubules in detergent-extracted apyrene spermatocytes ofEphestia kuehniella Z. Eur J Cell Biol 55: 238–247

    Google Scholar 

  • —, Kyburg J (1989) The restructuring of the flagellai base and the flagellar necklace during spermatogenesis ofEphestia kuehniella (Pyralidae, Lepidoptera). Cell Tissue Res 256: 77–86

    Google Scholar 

  • —, Spanel-Borowski K (1995) Acetylation of α-tubulin in different bovine cell types: implications for microtubule dynamics in interphase and mitosis. Cell Biol Int 19: 43–52

    Google Scholar 

  • —, Traut W (1991) Cytology of Lepidoptera. VII. The restructuring of eupyrene prophase I spermatocytes and its relationship to meiotic chromosome and spindle organization inEphestia kuehniella Z. Protoplasma 165: 51–63

    Google Scholar 

  • —, Baumgart K, Traut W (1987) Cytology of Lepidoptera. II. Fine structure of eupyrene and apyrene primary spermatocytes inOrgyia thyellina. Eur J Cell Biol 44: 57–67

    Google Scholar 

  • Wolf N, Regan CL, Fuller MT (1988) Temporal and spatial pattern of differences in microtubule behaviour duringDrosophila embryogenesis revealed by distribution of a tubulin isoform. Development 102: 311–324

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Wolf, K.W. Cytology of lepidoptera VIII. Acetylation of α-tubulin in mitotic and meiotic spindles of two Lepidoptera species,Ephestia kuehniella (Pyralidae) andPieris brassicae (Pieridae). Protoplasma 190, 88–98 (1996). https://doi.org/10.1007/BF01281197

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF01281197

Keywords

Navigation