|
|
|
|||
| Home Help Feedback Subscriptions Archive Search Table of Contents | ||||
First published online May 5, 2004
doi: 10.1242/10.1242/dev.01119
1 Kewalo Marine Laboratory, Pacific Biomedical Research Center, University of
Hawaii, 41 Ahui Street, Honolulu, HI 96813, USA
2 Department of Biology, Boston University, 5 Cummington Street, Boston, MA
02215, USA
* Author for correspondence (e-mail: mqmartin{at}hawaii.edu)
Accepted 11 February 2004
Mesoderm played a crucial role in the radiation of the triploblastic Bilateria, permitting the evolution of larger and more complex body plans than in the diploblastic, non-bilaterian animals. The sea anemone Nematostella is a non-bilaterian animal, a member of the phylum Cnidaria. The phylum Cnidaria (sea anemones, corals, hydras and jellyfish) is the likely sister group of the triploblastic Bilateria. Cnidarians are generally regarded as diploblastic animals, possessing endoderm and ectoderm, but lacking mesoderm. To investigate the origin of triploblasty, we studied the developmental expression of seven genes from Nematostella whose bilaterian homologs are implicated in mesodermal specification and the differentiation of mesodermal cell types (twist, snailA, snailB, forkhead, mef2, a GATA transcription factor and a LIM transcription factor). Except for mef2, the expression of these genes is largely restricted to the endodermal layer, the gastrodermis. mef2 is restricted to the ectoderm. The temporal and spatial expression of these `mesoderm' genes suggests that they may play a role in germ layer specification. Furthermore, the predominantly endodermal expression of these genes reinforces the hypothesis that the mesoderm and endoderm of triploblastic animals could be derived from the endoderm of a diploblastic ancestor. Alternatively, we consider the possibility that the diploblastic condition of cnidarians is a secondary simplification, derived from an ancestral condition of triploblasty.
Key words: Germlayer, Evolution, Nematostella vectensis, Cnidaria
This article has been cited by other articles:
![]() |
F. Rentzsch, J. H. Fritzenwanker, C. B. Scholz, and U. Technau FGF signalling controls formation of the apical sensory organ in the cnidarian Nematostella vectensis Development, May 15, 2008; 135(10): 1761 - 1769. [Abstract] [Full Text] [PDF] |
||||
![]() |
W. Shi and M. Levine Ephrin signaling establishes asymmetric cell fates in an endomesoderm lineage of the Ciona embryo Development, March 1, 2008; 135(5): 931 - 940. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. G. M. Extavour Evolution of the bilaterian germ line: lineage origin and modulation of specification mechanisms Integr. Comp. Biol., November 1, 2007; 47(5): 770 - 785. [Abstract] [Full Text] [PDF] |
||||
![]() |
F. Boero, B. Schierwater, and S. Piraino Cnidarian milestones in metazoan evolution Integr. Comp. Biol., November 1, 2007; 47(5): 693 - 700. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. G. M. Extavour Gray anatomy: phylogenetic patterns of somatic gonad structures and reproductive strategies across the Bilateria Integr. Comp. Biol., September 1, 2007; 47(3): 420 - 426. [Abstract] [Full Text] [PDF] |
||||
![]() |
N. H. Putnam, M. Srivastava, U. Hellsten, B. Dirks, J. Chapman, A. Salamov, A. Terry, H. Shapiro, E. Lindquist, V. V. Kapitonov, et al. Sea Anemone Genome Reveals Ancestral Eumetazoan Gene Repertoire and Genomic Organization Science, July 6, 2007; 317(5834): 86 - 94. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. M. Reitzel, J. C. Sullivan, and J. R. Finnerty Qualitative shift to indirect development in the parasitic sea anemone Edwardsiella lineata Integr. Comp. Biol., December 1, 2006; 46(6): 827 - 837. [Abstract] [Full Text] [PDF] |
||||
![]() |
P. Oliveri, K. D. Walton, E. H. Davidson, and D. R. McClay Repression of mesodermal fate by foxa, a key endoderm regulator of the sea urchin embryo Development, November 1, 2006; 133(21): 4173 - 4181. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. Q. Matus, K. Pang, H. Marlow, C. W. Dunn, G. H. Thomsen, and M. Q. Martindale From the Cover: Molecular evidence for deep evolutionary roots of bilaterality in animal development PNAS, July 25, 2006; 103(30): 11195 - 11200. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. A. Jenner Challenging received wisdoms: Some contributions of the new microscopy to the new animal phylogeny Integr. Comp. Biol., April 1, 2006; 46(2): 93 - 103. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. C. Sullivan, J. F. Ryan, J. A. Watson, J. Webb, J. C. Mullikin, D. Rokhsar, and J. R. Finnerty StellaBase: The Nematostella vectensis Genomics Database Nucleic Acids Res., January 1, 2006; 34(suppl_1): D495 - D499. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. G. Collins, P. Cartwright, C. S. McFadden, and B. Schierwater Phylogenetic Context and Basal Metazoan Model Systems Integr. Comp. Biol., August 1, 2005; 45(4): 585 - 594. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Barrallo-Gimeno and M. A. Nieto The Snail genes as inducers of cell movement and survival: implications in development and cancer Development, July 15, 2005; 132(14): 3151 - 3161. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. J. Peterson, M. A. McPeek, and D. A. D. Evans Tempo and mode of early animal evolution: inferences from rocks, Hox, and molecular clocks Paleobiology, June 1, 2005; 31(2_Suppl): 36 - 55. [Abstract] [Full Text] [PDF] |
||||