|
|
|
|||
| Home Help Feedback Subscriptions Archive Search Table of Contents | ||||
Development, Vol 118, Issue 3 665-690, Copyright © 1993 by Company of Biologists
JOURNAL ARTICLES |
EH Davidson
Division of Biology, California Institute of Technology, Pasadena 91125.
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.
This article has been cited by other articles:
![]() |
A. D. Smith, P. Sumazin, Z. Xuan, and M. Q. Zhang DNA motifs in human and mouse proximal promoters predict tissue-specific expression PNAS, April 18, 2006; 103(16): 6275 - 6280. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. P. Klingenberg, L. J. Leamy, and J. M. Cheverud Integration and Modularity of Quantitative Trait Locus Effects on Geometric Shape in the Mouse Mandible Genetics, April 1, 2004; 166(4): 1909 - 1921. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. Sherwood and D. McClay LvNotch signaling mediates secondary mesenchyme specification in the sea urchin embryo Development, January 4, 1999; 126(8): 1703 - 1713. [Abstract] [PDF] |
||||
![]() |
C. Logan, J. Miller, M. Ferkowicz, and D. McClay Nuclear beta-catenin is required to specify vegetal cell fates in the sea urchin embryo Development, January 1, 1999; 126(2): 345 - 357. [Abstract] [PDF] |
||||
![]() |
J Jernvall, T Aberg, P Kettunen, S Keranen, and I Thesleff The life history of an embryonic signaling center: BMP-4 induces p21 and is associated with apoptosis in the mouse tooth enamel knot Development, January 1, 1998; 125(2): 161 - 169. [Abstract] [PDF] |
||||
![]() |
D. Sherwood and D. McClay Identification and localization of a sea urchin Notch homologue: insights into vegetal plate regionalization and Notch receptor regulation Development, January 9, 1997; 124(17): 3363 - 3374. [Abstract] [PDF] |
||||
![]() |
H Benink, G Wray, and J Hardin Archenteron precursor cells can organize secondary axial structures in the sea urchin embryo Development, January 9, 1997; 124(18): 3461 - 3470. [Abstract] [PDF] |
||||
![]() |
C. Logan and D. McClay The allocation of early blastomeres to the ectoderm and endoderm is variable in the sea urchin embryo Development, January 6, 1997; 124(11): 2213 - 2223. [Abstract] [PDF] |
||||
![]() |
M. Arnone and E. Davidson The hardwiring of development: organization and function of genomic regulatory systems Development, January 5, 1997; 124(10): 1851 - 1864. [Abstract] [PDF] |
||||
![]() |
A. Melby, R. Warga, and C. Kimmel Specification of cell fates at the dorsal margin of the zebrafish gastrula Development, July 1, 1996; 122(7): 2225 - 2237. [Abstract] [PDF] |
||||
![]() |
E. H. Davidson, K. J. Peterson, and R. A. Cameron Origin of Bilaterian Body Plans: Evolution of Developmental Regulatory Mechanisms Science, November 24, 1995; 270(5240): 1319 - 1325. [Abstract] [PDF] |
||||
![]() |
G Salvatori, L Lattanzi, M Coletta, S Aguanno, E Vivarelli, R Kelly, G Ferrari, A. Harris, F Mavilio, M Molinaro, et al. Myogenic conversion of mammalian fibroblasts induced by differentiating muscle cells J. Cell Sci., January 8, 1995; 108(8): 2733 - 2739. [Abstract] [PDF] |
||||
![]() |
R. B. Goldberg, G. de Paiva, and R. Yadegari Plant Embryogenesis: Zygote to Seed Science, October 28, 1994; 266(5185): 605 - 614. [Abstract] [PDF] |
||||
![]() |
H. Chamberlin and P. Sternberg The lin-3/let-23 pathway mediates inductive signalling during male spicule development in Caenorhabditis elegans Development, January 10, 1994; 120(10): 2713 - 2721. [Abstract] [PDF] |
||||