The centrosome-attracting body, microtubule system, and posterior egg cytoplasm are involved in positioning of cleavage planes in the ascidian embryo

Dev Biol. 1999 May 1;209(1):72-85. doi: 10.1006/dbio.1999.9244.


Many kinds of animal embryos exhibit stereotyped cleavage patterns during early embryogenesis. In the ascidian Halocynthia roretzi, cleavage patterns are invariant but they are complicated by successive unequal cleavages that occur in the posterior region. Here we report the essential roles of a novel structure, called the centrosome-attracting body (CAB), which exists in the posterior pole cortex of cleaving embryos, in generating unequal cleavages. By removing and transplanting posterior egg cytoplasm and by treatment with sodium dodecyl sulfate, we demonstrated that loss of the CAB resulted in abolishment of unequal cleavage, while ectopic formation of the CAB caused ectopic unequal cleavages to occur. Experiments with a microtubule inhibitor demonstrated that the centrosome and nucleus were attracted toward the posterior cortex, where the CAB is located, by shortening of microtubule bundles formed between the centrosome and the CAB. Consequently, the mitotic apparatus was positioned asymmetrically, resulting in unequal cleavage. Immunohistochemistry provided evidence that a microtubule motor protein, a kinesin or kinesin-like molecule, may be associated with the CAB. Formation of the CAB during the early cleavage stage was resistant to treatment with the microtubule inhibitor. In contrast, the integrity of the CAB was lost upon treatment with a microfilament inhibitor. We propose that the CAB plays key roles in the orientation and positioning of cleavage planes during unequal cell division.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Actins / metabolism
  • Animals
  • Centrosome / physiology*
  • Cleavage Stage, Ovum / physiology*
  • Cytochalasin B / pharmacology
  • Cytoplasm / physiology*
  • Immunoblotting
  • Immunohistochemistry
  • Kinesin / antagonists & inhibitors
  • Kinesin / physiology
  • Microtubules / physiology*
  • Nocodazole / pharmacology
  • Sodium Dodecyl Sulfate / pharmacology
  • Time Factors
  • Urochordata / embryology*


  • Actins
  • Sodium Dodecyl Sulfate
  • Cytochalasin B
  • Kinesin
  • Nocodazole