|
|
|
|||
| Home Help Feedback Subscriptions Archive Search Table of Contents | ||||
Development, Vol 114, Issue 3 769-786, Copyright © 1992 by Company of Biologists
JOURNAL ARTICLES |
SD Reynolds, LM Angerer, J Palis, A Nasir and RC Angerer
Department of Biology, University of Rochester, NY 14627.
The cloning and characterization of cDNAs representing four genes or small gene families that are coordinately expressed in a spatially restricted pattern during the very early blastula (VEB) stage of sea urchin development are presented. The VEB genes encode multiple transcripts that are expressed transiently in embryos of Strongylocentrotus purpuratus between 16-cell stage and hatching, with peak abundance 12 to 15 hours post-fertilization (approximately 150-250 cells). The VEB transcripts share the same spatial pattern in the early blastula embryo: they are asymmetrically distributed along the animal-vegetal axis but their distribution around this axis is uniform. Thus, the VEB transcripts are the earliest messages to reveal asymmetry along the primary axis in the sea urchin embryo. The temporal and spatial patterns of VEB transcript accumulation are not consistent with involvement of these gene products in cell division or in tissue-specific functions. Furthermore, VEB messages cannot be detected in either ovary or adult tissues, suggesting that these genes function exclusively during embryogenesis. We suggest that the VEB genes function in constructing the early blastula. Two VEB genes encode metalloendoproteases: one (SpHE) is hatching enzyme and the other (SpAN) is similar to bone morphogenetic protein-1 (BMP-1; Wozney et al., Science 242: 1528-1534, 1988) and the Tolloid gene product (tld) (Shimell et al., Cell 67: 459-482, 1991). Several lines of evidence suggest that the VEB genes are regulated directly by factors or regulatory activities localized along the maternally specificed animal-vegetal axis.
This article has been cited by other articles:
![]() |
L. M. Angerer, D. W. Oleksyn, A. M. Levine, X. Li, W. H. Klein, and R. C. Angerer Sea urchin goosecoid function links fate specification along the animal-vegetal and oral-aboral embryonic axes Development, November 15, 2001; 128(22): 4393 - 4404. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. R. Sherwood and D. R. McClay LvNotch signaling plays a dual role in regulating the position of the ectoderm-endoderm boundary in the sea urchin embryo Development, June 15, 2001; 128(12): 2221 - 2232. [Abstract] [Full Text] [PDF] |
||||
![]() |
E. Howard, L. Newman, D. Oleksyn, R. Angerer, and L. Angerer SpKrl: a direct target of beta-catenin regulation required for endoderm differentiation in sea urchin embryos Development, January 2, 2001; 128(3): 365 - 375. [Abstract] [PDF] |
||||
![]() |
L Yan, K Fei, J Zhang, S Dexter, and M. Sarras Identification and characterization of hydra metalloproteinase 2 (HMP2): a meprin-like astacin metalloproteinase that functions in foot morphogenesis Development, January 1, 2000; 127(1): 129 - 141. [Abstract] [PDF] |
||||
![]() |
Z. Wei, R. C. Angerer, and L. M. Angerer Identification of a New Sea Urchin Ets Protein, SpEts4, by Yeast One-Hybrid Screening with the Hatching Enzyme Promoter Mol. Cell. Biol., February 1, 1999; 19(2): 1271 - 1278. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Kenny, D Kozlowski, D. Oleksyn, L. Angerer, and R. Angerer SpSoxB1, a maternally encoded transcription factor asymmetrically distributed among early sea urchin blastomeres Development, January 12, 1999; 126(23): 5473 - 5483. [Abstract] [PDF] |
||||
![]() |
Y. Lee, G. Huang, R. Cameron, G Graham, E. Davidson, L Hood, and R. Britten EST analysis of gene expression in early cleavage-stage sea urchin embryos Development, January 9, 1999; 126(17): 3857 - 3867. [Abstract] [PDF] |
||||
![]() |
M Di Bernardo, S Castagnetti, D Bellomonte, P Oliveri, R Melfi, F Palla, and G Spinelli Spatially restricted expression of PlOtp, a Paracentrotus lividus orthopedia-related homeobox gene, is correlated with oral ectodermal patterning and skeletal morphogenesis in late-cleavage sea urchin embryos Development, January 5, 1999; 126(10): 2171 - 2179. [Abstract] [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] |
||||
![]() |
Z Wei, L. Angerer, and R. Angerer Spatially regulated SpEts4 transcription factor activity along the sea urchin embryo animal-vegetal axis Development, January 4, 1999; 126(8): 1729 - 1737. [Abstract] [PDF] |
||||
![]() |
E. Davidson, R. Cameron, and A Ransick Specification of cell fate in the sea urchin embryo: summary and some proposed mechanisms Development, January 9, 1998; 125(17): 3269 - 3290. [Abstract] [PDF] |
||||
![]() |
C.-H. Hung, H.-R. Huang, C.-J. Huang, F.-L. Huang, and G.-D. Chang Purification and Cloning of Carp Nephrosin, a Secreted Zinc Endopeptidase of the Astacin Family J. Biol. Chem., May 23, 1997; 272(21): 13772 - 13778. [Abstract] [Full Text] [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] |
||||
![]() |
N Suzuki, P. Labosky, Y Furuta, L Hargett, R Dunn, A. Fogo, K Takahara, D. Peters, D. Greenspan, and B. Hogan Failure of ventral body wall closure in mouse embryos lacking a procollagen C-proteinase encoded by Bmp1, a mammalian gene related to Drosophila tolloid Development, January 11, 1996; 122(11): 3587 - 3595. [Abstract] [PDF] |
||||
![]() |
L Yan, G. Pollock, H Nagase, and M. Sarras A 25.7 x 10(3) M(r) hydra metalloproteinase (HMP1), a member of the astacin family, localizes to the extracellular matrix of Hydra vulgaris in a head-specific manner and has a developmental function Development, January 6, 1995; 121(6): 1591 - 1602. [Abstract] [PDF] |
||||
![]() |
D M Kingsley The TGF-beta superfamily: new members, new receptors, and new genetic tests of function in different organisms. Genes & Dev., January 15, 1994; 8(2): 133 - 146. [PDF] |
||||
![]() |
B Spencer-Dene, P Thorogood, S Nair, A. Kenny, M Harris, and B Henderson Distribution of, and a putative role for, the cell-surface neutral metallo-endopeptidases during mammalian craniofacial development Development, January 11, 1994; 120(11): 3213 - 3226. [Abstract] [PDF] |
||||
![]() |
A. Finelli, C. Bossie, T Xie, and R. Padgett Mutational analysis of the Drosophila tolloid gene, a human BMP-1 homolog Development, January 4, 1994; 120(4): 861 - 870. [Abstract] [PDF] |
||||
![]() |
S. Hwang, J. Partin, and W. Lennarz Characterization of a homolog of human bone morphogenetic protein 1 in the embryo of the sea urchin, Strongylocentrotus purpuratus Development, January 3, 1994; 120(3): 559 - 568. [Abstract] [PDF] |
||||
![]() |
N. Mozingo, L. Hollar, and D. Chandler Degradation of an extracellular matrix: sea urchin hatching enzyme removes cortical granule-derived proteins from the fertilization envelope J. Cell Sci., January 3, 1993; 104(3): 929 - 938. [Abstract] [PDF] |
||||
![]() |
N. R. Barton, E. M. Bonder, D. J. Fishkind, R. H. Warren, and M. M. Pratt A novel vesicle-associated protein (VAP-1) in sea urchin eggs containing multiple RNA-binding consensus sequences J. Cell Sci., November 1, 1992; 103(3): 797 - 809. [Abstract] [PDF] |
||||
![]() |
S. Amano, I. C. Scott, K. Takahara, M. Koch, M.-F. Champliaud, D. R. Gerecke, D. R. Keene, D. L. Hudson, T. Nishiyama, S. Lee, et al. Bone Morphogenetic Protein 1 Is an Extracellular Processing Enzyme of the Laminin 5 gamma 2 Chain J. Biol. Chem., July 21, 2000; 275(30): 22728 - 22735. [Abstract] [Full Text] [PDF] |
||||
![]() |
L. Garrigue-Antar, C. Barker, and K. E. Kadler Identification of Amino Acid Residues in Bone Morphogenetic Protein-1 Important for Procollagen C-proteinase Activity J. Biol. Chem., July 6, 2001; 276(28): 26237 - 26242. [Abstract] [Full Text] [PDF] |
||||