3 Sea Urchin Microtubules

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From the first demonstration that the mitotic apparatus could be isolated as a discrete entity, to the identification of the colchicine-binding protein, tubulin, to the purification of an mRNA-polyribosome-microtubule complex, sea urchin eggs and embryos have been a model system for the study of microtubule formation and function during the cell cycle. Sea urchins can be induced to spawn in the laboratory, yielding a great volume of eggs that contain a large amount of unassembled tubulin subunits and few detectable microtubules. These eggs can be fertilized in vitro and within a short period of time, the microtubules of the mitotic apparatus assemble and disassemble with remarkable synchrony throughout the early cleavage divisions. Thus, sea urchin eggs are viewed as an inducible model system for studying microtubule assembly and disassembly during the embryonic cleavage cycles. This chapter focuses on the molecular components that may regulate microtubule formation and function during the embryonic cell cycles and cytoplasmic microtubule arrays are also considered.

References (206)

  • D. Alexandraki et al.

    Sequence heterogeneity, multiplicity, and genomic organization of α- and β-tubulin genes in sea urchins

    Mol. Cell. Biol.

    (1981)
  • D. Alexandraki et al.

    Evolution of α- and β-tubulin genes as inferred by the nucleotide sequences of sea urchin cDNA clones

    J. Mol. Evol.

    (1983)
  • D. Alexandraki et al.

    Expression of α- and β-tubulin genes during development of sea urchin embryos

    Dev. Biol.

    (1985)
  • D. Alexandraki et al.

    Multiple polymorphic α- and β-tubulin mRNAs are present in sea urchin eggs

    Proc. Natl. Acad. Sci. USA

    (1985)
  • J.A. Anstrom

    Sea urchin primary mesenchyme cells: Ingression occurs independent of microtubules

    Dev. Biol.

    (1989)
  • C.F. Asnes et al.

    Analysis of microtubule polymerization inhibitors in sea urchin egg extracts: Evidence for a protease

    Arch. Biochem. Biophys.

    (1981)
  • W. Auclair et al.

    Cilia regeneration in the sea urchin blastula

    Science

    (1966)
  • R. Balczon et al.

    Microtubule-containing detergent-extracted cytoskeletons in sea urchin eggs from fertilization through cell division: Anti-tubulin immunofluorescence microscopy

    Cell Motil.

    (1983)
  • L.D. Belmont et al.

    Real-time visualization of cell cycle-dependent changes in microtubule dynamics in cytoplasmic extracts

    Cell

    (1990)
  • T.H. Bestor et al.

    Anti-tubulin immunofluorescence microscopy of microtubules present during the pronuclear movements of sea urchin fertilization

    Dev. Biol.

    (1981)
  • T.H. Bestor et al.

    Configurations of microtubules in artificially activated eggs of the sea urchin Lytechinus variegatus

    Exp. Cell Res.

    (1982)
  • T. Bibring et al.

    Tubulin synthesis in sea urchin embryos: Almost all tubulin of the first cleavage mitotic apparatus derives from the unfertilized egg

    Dev. Biol.

    (1977)
  • T. Bibring et al.

    Tubulin synthesis in sea urchin embryos II. Ciliary A tubulin derives from the unfertilized egg

    Dev. Biol.

    (1981)
  • G.S. Bloom et al.

    Microtubule-associated proteins in the sea-urchin egg mitotic spindle

  • G.S. Bloom et al.

    Use of multiple monoclonal antibodies to chracterize the major microtubule-associated protein in sea urchin eggs

    Cell Motil.

    (1985)
  • G.S. Bloom et al.

    Isolation of mitotic microtubule-associated proteins from sea urchin eggs

    Ann. N.Y. Acad. Sci.

    (1985)
  • G.G. Borisy et al.

    The mechanism of action of colchicine. Colchicine binding to sea urchin eggs and the mitotic apparatus

    J. Cell Biol.

    (1967)
  • G.G. Borisy et al.

    Purification of tubulin and associated high molecular weight proteins from porcine brain and characterization of microtubule assembly in vitro

    Ann. N.Y. Acad. Sci.

    (1975)
  • J.A. Boyle et al.

    Sea urchin oocytes possess elaborate cortical arrays of microfilaments, microtubules and intermediate filaments

    Dev. Biol.

    (1989)
  • J. Bryan et al.

    Inhibition of tubulin assembly by RNA and other polyanions: Evidence for a required protein

    Proc. Natl. Acad. Sci. USA

    (1975)
  • J.C. Bulinski et al.

    Stabilization and post-translational modification of microtubules during cellular morphogenesis

    Bio Essays

    (1991)
  • L.U. Cassimeris et al.

    Real-time observations of microtubule dynamic instability in living cells

    J. Cell Biol.

    (1988)
  • D.W. Cleveland et al.

    Molecular biology and genetics of tubulin

    Annu. Rev. Biochem.

    (1985)
  • D.W. Cleveland et al.

    Regulation of tubulin synthesis

  • G. Cogneti et al.

    Studies of protein synthesis during sea urchin oogenesis. II. Synthesis of tubulin

    Cell Differ.

    (1977)
  • C.A. Collins et al.

    A microtubule-activated ATPase from sea urchin eggs, distinct from cytoplasmic dynein and kinesin

    Proc. Natl. Acad. Sci. USA

    (1986)
  • L. Cooley et al.

    Cytoskeletal functions during Drosophila oogenesis

    Science

    (1994)
  • E.H. Davidson

    Gene Activity in Early Development.

    (1986)
  • W.L. Dentler

    Cilia and flagella

    Int. Rev. Cytol. Suppl.

    (1987)
  • H.W. Detrich

    Isolation of sea urchin egg tubulin

    Methods Enzymol.

    (1986)
  • H.W. Detrich et al.

    Purification, characterization, and assembly properties of tubulin from unfertilized eggs of the sea urchin Strongylocentrotus purpuratus

    Biochemistry

    (1983)
  • M.G. Di Bernardo et al.

    Nucleotide sequence of a full length cDNA clone encoding for β-tubulin of the sea urchin Paracentrotus lividus

    Nucleic Acids Res.

    (1989)
  • J.H. Dinsmore et al.

    Calcium and calmodulin-dependent phosphorylation of a 62-kDa protein induces microtubule depolymerization in sea urchin mitotic apparatuses

    Cell

    (1988)
  • J.H. Dinsmore et al.

    Microinjection of antibodies to a 62-kDa mitotic apparatus protein arrests mitosis in dividing sea urchin embryos

    Cell

    (1989)
  • J. Drawbridge et al.

    Identification and characterization of the poly(A)-binding proteins from the sea urchin: A quantitative analysis

    Mol. Cell. Biol.

    (1990)
  • L. Dufresne et al.

    Effects of 6-dimethylaminopurine on microtubules and putative intermediate filaments in sea urchin embryos

    J. Cell Sci.

    (1991)
  • B.D. Dynlacht et al.

    The dTAF1180 subunit of Drosophila TF11D contains β-transducin repeats

    Nature

    (1993)
  • K.T. Edds

    Morphological and cytoskeletal transformation in sea urchin coelomocytes

  • K. Faire et al.

    Sea urchin egg 100-kDa dynamin-related protein: Identification of and localization to intracellular vesicles

    Dev. Biol.

    (1993)
  • H.K.W. Fong et al.

    Repetitive segmental structure of the transducin β subunit: Homology with the CDC4 gene and identification of related mRNAs

    Proc. Natl. Acad. Sci. USA

    (1986)
  • A. Forer et al.

    Characteristics of sea urchin mitotic apparatus isolated using dimethyl sulphoxide/glycerol medium

    J. Cell Sci.

    (1974)
  • F. Gianguzza et al.

    DNA sequence and pattern of expression of the sea urchin (Paracentrotuslividus) alpha-tubulin genes

    Mol. Reprod. Dev.

    (1989)
  • F. Gianguzza et al.

    Sequence and expression of Paracentrotus lividus α tubulin gene

    Nucleic Acids Res.

    (1990)
  • J.R. Gibbins et al.

    Microtubules in the formation and development of the primary mesenchyme in Arbacia punctulaia

    J. Cell Biol.

    (1969)
  • N.R. Gliksman et al.

    Okadaic acid induces interphase to mitotic-like microtubule dynamic instability by inactivating rescue

    J. Cell Biol.

    (1992)
  • N.R. Gliksman et al.

    Cytoplasmic extracts from the eggs of sea urchins and clams for the study of microtubule-associated motility and bundling

    Methods Cell Biol.

    (1993)
  • R.D. Goldman et al.

    The structure and some properties of the isolated mitotic apparatus

    J. Cell Sci.

    (1969)
  • Z.Y. Gong et al.

    Stabilization of tubulin mRNA by inhibition of protein synthesis in sea urchin embryos

    Mol. Cell Biol.

    (1988)
  • Z.Y. Gong et al.

    Autogenous regulation of tubulin synthesis via RNA stability during sea urchin embryogenesis

    Development

    (1988)
  • Z.Y. Gong et al.

    Microtubule formation from maternal tubulins during sea urchin embryogenesis: Measurement of soluble and insoluble pools

    Mol. Reprod. Dev.

    (1988)
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