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PMID: 10662649 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

A BMP pathway regulates cell fate allocation along the sea urchin animal-vegetal embryonic axis.

Development (Cambridge, England) ·Vol. 127 ·No. 5 ·2000-03-00 ·Pages 1105-14

Angerer LM, Oleksyn DW, Logan CY, McClay DR, Dale L, Angerer RC

Abstract

To examine whether a BMP signaling pathway functions in specification of cell fates in sea urchin embryos, we have cloned sea urchin BMP2/4, analyzed its expression in time and space in developing embryos and assayed the developmental consequences of changing its concentration through mRNA injection experiments. These studies show that BMP4 mRNAs accumulate transiently during blastula stages, beginning around the 200-cell stage, 14 hours postfertilization. Soon after the hatching blastula stage, BMP2/4 transcripts can be detected in presumptive ectoderm, where they are enriched on the oral side. Injection of BMP2/4 mRNA at the one-cell stage causes a dose-dependent suppression of commitment of cells to vegetal fates and ectoderm differentiates almost exclusively as a squamous epithelial tissue. In contrast, NOGGIN, an antagonist of BMP2/4, enhances differentiation of endoderm, a vegetal tissue, and promotes differentiation of cells characteristic of the ciliated band, which contains neurogenic ectoderm. These findings support a model in which the balance of BMP2/4 signals produced by animal cell progeny and opposing vegetalizing signals sent during cleavage stages regulate the position of the ectoderm/ endoderm boundary. In addition, BMP2/4 levels influence the decision within ectoderm between epidermal and nonepidermal differentiation.

MeSH Terms
Amino Acid Sequence Animals Body Patterning/physiology Bone Morphogenetic Protein 2 Bone Morphogenetic Protein 4 Bone Morphogenetic Proteins/chemistry,genetics,physiology Cloning, Molecular Ectoderm/physiology Embryo, Nonmammalian/physiology Endoderm/physiology Gene Expression Regulation, Developmental Molecular Sequence Data Oocytes/physiology RNA, Messenger/genetics Recombinant Proteins/biosynthesis Sea Urchins/embryology,genetics Sequence Alignment Sequence Homology, Amino Acid Transcription, Genetic Transforming Growth Factor beta Xenopus Xenopus Proteins
Chemicals
Bone Morphogenetic Protein 2 Bone Morphogenetic Protein 4 Bone Morphogenetic Proteins RNA, Messenger Recombinant Proteins Transforming Growth Factor beta Xenopus Proteins bmp4 protein, Xenopus
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Angerer L M
Department of Biology, University of Rochester, Rochester, NY 14627, USA. [email protected]
Oleksyn D W
Logan C Y
McClay D R
Dale L
Angerer R C
Article Info
Journal
Development (Cambridge, England)
Abbr.
Development
ISSN
0950-1991
Published
2000-03-00
Pages
1105-14
Language
English
Region
England
NLM ID
8701744
Subset
IM
Grants
NIGMS NIH HHS · GM25553 · United States
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