Hostname: page-component-745bb68f8f-b6zl4 Total loading time: 0 Render date: 2025-02-11T01:41:16.690Z Has data issue: false hasContentIssue false

Regulative potential to form an amniotic cavity in mesomeres of a direct developing echinoid, Peronella japonica

Published online by Cambridge University Press:  16 July 2018

Chisato Kitazawa
Affiliation:
Department of Biological Sciences, Graduate School of Science, University of Tokyo, Japan
Shonan Amemiya
Affiliation:
Department of Biological Sciences, Graduate School of Science, University of Tokyo, Japan Department of Integrated Biosciences, Graduate School of Frontier Sciences, University of Tokyo, Japan
Rights & Permissions [Opens in a new window]

Extract

Core share and HTML view are not available for this content. However, as you have access to this content, a full PDF is available via the ‘Save PDF’ action button.

Peronella japonica, a direct developer, exhibits certain peculiar features during development, particularly heterochrony, a change in the relative timing of expression among tissues and organs. One of the important heterochronical changes in the species was found in the development of the amniotic cavity, a component of an adult rudiment. In indirect developers the amniotic cavity is formed on the left side of the larval body in the late pluteus stage. In P. japonica the organ is formed at the gastrula stage in the region located on the midline of the larval body.

In the present study, the ability of partial embryos isolated from 8- or 16-cell stage embryos of P. japonica to differentiate an amniotic cavity was investigated to assess the regulative potential of a direct developer.

The embryos were dissected at 8-cell stage with a glass needle to obtain half embryos. Some of the half embryos were further divided into four blastomeres to obtain mesomere pairs. Each half embryo and blastomere that did not form micromeres but divided equally during the next cleavage was identified as an animal cap and presumptive mesomere pair. Isolated animal caps and mesomere pairs were cultured, and differentiation of the amniotic cavity was examined at 24 and 48 h after fertilisation, when the organ in the normal embryos had already completed differentiation.

Type
Special Lecture for Citizens
Copyright
Copyright © Cambridge University Press 1999