The A/P axis in echinoderm ontogeny and evolution: evidence from fossils and molecules
Abstract
SUMMARY Even though echinoderms are members of the Bilateria, the location of their anterior/posterior axis has remained enigmatic. Here we propose a novel solution to the problem employing three lines of evidence: the expression of a posterior class Hox gene in the coeloms of the nascent adult body plan within the larva; the anatomy of certain early fossil echinoderms; and finally the relation between endoskeletal plate morphology and the associated coelomic tissues. All three lines of evidence converge on the same answer, namely that the location of the adult mouth is anterior, and the anterior/posterior axis runs from the mouth through the adult coelomic compartments. This axis then orients the animal such that there is but a single plane of symmetry dividing the animal into left and right halves. We tentatively hypothesize that this plane of symmetry is positioned along the dorsal/ventral axis. These axis identifications lead to the conclusion that the five ambulacra are not primary body axes, but instead are outgrowths from the central anterior/posterior axis. These identifications also shed insight into several other evolutionary mysteries of various echinoderm clades such as the independent evolution of bilateral symmetry in irregular echinoids, but do not elucidate the underlying mechanisms of the adult coelomic architecture.
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Topological similarity strongly suggests homology within Ambulacraria but not homology between any other higher taxa.
“when it is, it strongly suggests homology, for example, within Ambulacraria (Peterson et al. 2000; Smith et al. 2004), but not homology between any other higher taxa (Ruppert 1991; Nielsen 2001).”
From The Ediacaran emergence of bilaterians: congruence between the genetic and the geological fossil records (2008) · cites this paper as Peterson et al. 2000
Cites
Origin of Bilaterian Body Plans: Evolution of Developmental Regulatory Mechanisms
Davidson, E. H., Peterson, K. J., & Cameron, R. A. (1995) · Science · doi:10.1126/science.270.5240.1319 · Cited by 381 · cited 1× · see citing works
“…developing embryos/larvae and the body plans of adult forms arise directly from the utilization of set-aside cells, the progeny of which produce the adult body plan, and which are mounted within the embryo at various angles to the embryo/larval axis (Davidson et al. 1995; Peterson et al. 1997).”
BackgroundSelf-citationSet‐aside cells in maximal indirect development: Evolutionary and developmental significance
Peterson, K. J., Cameron, R. A., & Davidson, E. H. (1997) · BioEssays · doi:10.1002/bies.950190713 · Cited by 164 · see citing works
Self-citationBilaterian Origins: Significance of New Experimental Observations
Peterson, K. J., Cameron, R. A., & Davidson, E. H. (2000) · Developmental Biology · doi:10.1006/dbio.1999.9475 · Cited by 133 · see citing works
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Peterson, K. J., Cotton, J. A., Gehling, J. G., & Pisani, D. (2008) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2007.2233 · Cited by 313 · see citing works
Self-citationPETERSON, K. J., SUMMONS, R. E., & DONOGHUE, P. C. J. (2007) · Palaeontology · doi:10.1111/j.1475-4983.2007.00692.x · Cited by 93 · see citing works
Self-citationThe mouth, the anus, and the blastopore—open questions about questionable openings
Hejnol, A., & Martindale, M. Q. (2009) · Animal Evolution · doi:10.1093/acprof:oso/9780199549429.003.0004 · Cited by 37 · see citing works
Genomic, phylogenetic, and cell biological insights into metazoan origins
Nichols, S. A., Dayel, M. J., & King, N. (2009) · Animal Evolution · doi:10.1093/acprof:oso/9780199549429.003.0003 · Cited by 24 · see citing works
- Authors
- Peterson, K. J., Arenas‐Mena, C., & Davidson, E. H.
- Venue
- Evolution & Development
- Publisher
- Wiley
- Published
- 2000-03
- Volume
- 2
- Issue
- 2
- Pages
- 93-101
- ISSN
- 1520-541X
- 1525-142X
- Cited by
- 83
- References
- 3
- Language
- en
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