Welcome to the new version of CaltechAUTHORS. Login is currently restricted to library staff. If you notice any issues, please email coda@library.caltech.edu
Published July 1993 | Published
Journal Article Open

Later embryogenesis: regulatory circuitry in morphogenetic fields

Abstract

The subject of this review is the nature of regulatory processes underlying the spatial subdivision of morphogenetic regions in later embryogenesis. I have applied a non-classical definition of morphogenetic field, the progenitor field, which is a region of an embryo composed of cells whose progeny will constitute a given morphological structure. An important feature of such fields is that they have sharp spatial boundaries, across which lie cells whose progeny will express different fates. Two examples of the embryonic specification and development of such fields are considered. These are the formation of the archenteron in the sea urchin embryo and the formation of dorsal axial mesoderm in the Xenopus embryo. From these and a number of additional examples, from vertebrate, Drosophila, Caenorhabditis elegans and sea urchin embryos, it is concluded that the initial formation of the boundaries of morphogenetic progenitor fields depends on both positive and negative transcription control functions. Specification of morphogenetic progenitor fields, organization of the boundaries and their subsequent regionalization or subdivision are mediated by intercellular signaling. Genes encoding regionally expressed transcription factors that are activated in response to intercell signaling, and that in turn mediate signaling changes downstream, appear as fundamental regulatory circuit elements. Such [signal-->transcription factor gene-->signal] circuit elements appear to be utilized, often repetitively, in many different morphogenetic processes.

Additional Information

© 1993 The Company of Biologists Limited. Accepted 9 March 1993. I am immeasurably indebted to many colleagues, for their thoughtfulness, their wisdom and their perspicacity in guiding me to improvements of drafts of this manuscript. For their interest and extensive efforts, and the marvelous discussions this project occasioned, I particularly wish to thank Richard Axel, of the HHMI at Columbia University; Marianne Bronner-Fraser, of UC Irvine; Roy Britten of Caltech; Andrew Cameron of Caltech; Scott Fraser of Caltech; Mike Levine of UC San Diego; David Kimelman of the University of Washington; Ellen Rothenberg of Caltech; and Paul Sternberg of Caltech. Research from this laboratory was supported by an NIH grant (HD-05753).

Attached Files

Published - DAVdev93.pdf

Files

DAVdev93.pdf
Files (360.7 kB)
Name Size Download all
md5:3cb602ce8542b74b225bf29c8bedd251
360.7 kB Preview Download

Additional details

Created:
August 20, 2023
Modified:
October 24, 2023