The Wnt/calcium pathway activates NF-AT and promotes ventral cell fate in Xenopus embryos
Abstract
It is thought that inositol-1,4,5-trisphosphate (Ins(1,4,5)P(3))-Ca(2+) signalling has a function in dorsoventral axis formation in Xenopus embryos; however, the immediate target of free Ca(2+) is unclear. The secreted Wnt protein family comprises two functional groups, the canonical Wnt and Wnt/Ca(2+) pathways. The Wnt/Ca(2+) pathway interferes with the canonical Wnt pathway, but the underlying molecular mechanism is poorly understood. Here, we cloned the complementary DNA coding for the Xenopus homologue of nuclear factor of activated T cells (XNF-AT). A gain-of-function, calcineurin-independent active XNF-AT mutation (CA XNF-AT) inhibited anterior development of the primary axis, as well as Xwnt-8-induced ectopic dorsal axis development in embryos. A loss-of-function, dominant negative XNF-AT mutation (DN XNF-AT) induced ectopic dorsal axis formation and expression of the canonical Wnt signalling target molecules siamois and Xnr3 (ref. 4). Xwnt-5A induced translocation of XNF-AT from the cytosol to the nucleus. These data indicate that XNF-AT functions as a downstream target of the Wnt/Ca(2+) and Ins(1,4,5)P(3)-Ca(2+) pathways, and has an essential role in mediating ventral signals in the Xenopus embryo through suppression of the canonical Wnt pathway.
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CamKII activates the transcription factor NFAT to promote ventral cell fates in the Xenopus embryo.
“CamK11 have been shown to activate the transcription factor NFAT to promote ventral cell fates in the Xenopus embryo.98”
From Wnt signal transduction pathways (2008) · cites this paper as [98]
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- Authors
- Saneyoshi, T., Kume, S., Amasaki, Y., & Mikoshiba, K.
- Affiliations
- Institute of Medical Science, The University of Tokyo (JP)
- Japan Science and Technology Agency (JP)
- RIKEN Center for Brain Science (JP)
- Corresponding author
- Kume, Shoen
- Mikoshiba, Katsuhiko
- Venue
- Nature
- Published
- 2002-05
- Volume
- 417
- Issue
- 6886
- Pages
- 295-299
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- OpenAlex
- W2000352591
- Cited by
- 322
- References
- 30
- Citations by year
- 2026: 6 · 2025: 6 · 2024: 3 · 2023: 5 · 2022: 8 · 2021: 8 · 2020: 11 · 2019: 3 · 2018: 7 · 2017: 10 · 2016: 10 · 2015: 12 · 2014: 17 · 2013: 19 · 2012: 14
- FWCI
- 8.44
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- Tokyo Tech Research Repository (Tokyo Institute of Technology) (submittedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Wnt/β-catenin signaling in development and cancer
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Signaling Pathways in Disease
- Keywords
- Wnt/Ca2+ pathway, NFAT, calcium signaling, inositol 1,4,5-trisphosphate, canonical Wnt pathway, Siamois, Xenopus embryo, nuclear translocation
- MeSH terms
- Animals, DNA-Binding Proteins, Models, Biological, Molecular Sequence Data, Nuclear Proteins, Proto-Oncogene Proteins, RNA, Messenger, Transcription Factors, Xenopus laevis, Inositol 1,4,5-Trisphosphate, Cell Lineage, Body Patterning, Calcineurin, Calcium Signaling, Reverse Transcriptase Polymerase Chain Reaction, Protein Transport, Xenopus Proteins, Zebrafish Proteins, NFATC Transcription Factors, Wnt Proteins
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