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Nuclear β-catenin is required to specify vegetal cell fates in the sea urchin embryo
Abstract
β-catenin is thought to mediate cell fate specification events by localizing to the nucleus where it modulates gene expression. To ask whether β-catenin is involved in cell fate specification during sea urchin embryogenesis, we analyzed the distribution of nuclear β-catenin in both normal and experimentally manipulated embryos. In unperturbed embryos, β-catenin accumulates in nuclei that include the precursors of the endoderm and mesoderm, suggesting that it plays a role in vegetal specification. Using pharmacological, embryological and molecular approaches, we determined the function of β-catenin in vegetal development by examining the relationship between the pattern of nuclear β-catenin and the formation of endodermal and mesodermal tissues. Treatment of embryos with LiCl, a known vegetalizing agent, caused both an enhancement in the levels of nuclear β-catenin and an expansion in the pattern of nuclear β-catenin that coincided with an increase in endoderm and mesoderm. Conversely, overexpression of a sea urchin cadherin blocked the accumulation of nuclear β-catenin and consequently inhibited the formation of endodermal and mesodermal tissues including micromere-derived skeletogenic mesenchyme. In addition, nuclear β-catenin-deficient micromeres failed to induce a secondary axis when transplanted to the animal pole of uninjected host embryos, indicating that nuclear β-catenin also plays a role in the production of micromere-derived signals. To examine further the relationship between nuclear β-catenin in vegetal nuclei and micromere signaling, we performed both transplantations and deletions of micromeres at the 16-cell stage and demonstrated that the accumulation of β-catenin in vegetal nuclei does not require micromere-derived cues. Moreover, we demonstrate that cell autonomous signals appear to regulate the pattern of nuclear β-catenin since dissociated blastomeres possessed nuclear β-catenin in approximately the same proportion as that seen in intact embryos. Together, these data show that the accumulation of β-catenin in nuclei of vegetal cells is regulated cell autonomously and that this localization is required for the establishment of all vegetal cell fates and the production of micromere-derived signals.
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Cites
Lithium inhibits glycogen synthase kinase-3 activity and mimics wingless signalling in intact cells
Stambolic, V., Ruel, L., & Woodgett, J. R. (1996) · Current Biology · doi:10.1016/s0960-9822(02)70790-2 · Cited by 1,321
How embryos work: a comparative view of diverse modes of cell fate specification
Davidson, E. H. (1990) · Development · doi:10.1242/dev.108.3.365 · Cited by 267
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Metadata
- Authors
- Logan, C. Y., Miller, J. R., Ferkowicz, M. J., & McClay, D. R.
- Venue
- Development
- Publisher
- The Company of Biologists
- Published
- 1999-01-15
- Volume
- 126
- Issue
- 2
- Pages
- 345-357
- ISSN
- 0950-1991 (ISSN-L)
- 1477-9129
- OpenAlex
- W2117799366
- Cited by
- 456
- References
- 2
- FWCI
- 7.83
- Type
- journal article
- Language
- en
- Open access
- closed
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- Logan, C. Y., Miller, J. R., Ferkowicz, M. J., & McClay, D. R. (1999). Nuclear β-catenin is required to specify vegetal cell fates in the sea urchin embryo. Development. https://doi.org/10.1242/dev.126.2.345
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