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Polarized Translocation of Fluorescent Proteins in Xenopus Ectoderm in Response to Wnt Signaling
Published on: May 26, 2011
Wnt signaling polarizes an early C. elegans blastomere to distinguish endoderm from mesoderm
C J Thorpe1, A Schlesinger, J C Carter
1Institute of Molecular Biology, University of Oregon, Eugene 97403, USA.
Abstract:
A polarizing signal induces endoderm production by a 4-cell stage blastomere in C. elegans called EMS. We identified 16 mutations in five genes, mom-1 through mom-5, required for EMS to produce endoderm. mom-1, mom-2, and mom-3 are required in the signaling cell, P2, while mom-4 is required in EMS. P2 signaling downregulates an HMG domain protein, POP-1, in one EMS daughter. The sequence of mom-2 predicts that it encodes a member of the Wnt family of secreted glycoproteins, which in other systems activate HMG domain proteins. Defective mitotic spindle orientations in mom mutant embryos indicate that Wnt signaling influences cytoskeletal polarity in blastomeres throughout the early embryo.
Insights
Five genes (mom-1 to mom-5) are crucial for endoderm development in C. elegans. This Wnt signaling pathway regulates cell polarity and gene expression in early embryonic blastomeres.
Area of Science:
- Developmental Biology
- Cell Biology
- Genetics
Background:
- A polarizing signal at the 4-cell stage in C. elegans directs the EMS blastomere to produce endoderm.
- The molecular mechanisms governing this asymmetric cell fate determination are not fully understood.
Purpose of the Study:
- To identify genes essential for endoderm production by the EMS blastomere in C. elegans.
- To elucidate the role of signaling pathways in establishing cell polarity during early embryogenesis.
Main Methods:
- Forward genetic screen to identify mutations affecting endoderm development.
- Analysis of gene function in specific blastomeres (P2 signaling cell and EMS).
- Examination of mitotic spindle orientation in mutant embryos.
Main Results:
- Identified 16 mutations in five genes (mom-1 to mom-5) required for EMS-induced endoderm production.
- mom-1, mom-2, and mom-3 function in the P2 signaling cell, while mom-4 acts in the EMS blastomere.
- P2 signaling downregulates the HMG domain protein POP-1 in an EMS daughter cell.
- mom-2 encodes a Wnt family member, suggesting a conserved signaling pathway.
- Mutations disrupt mitotic spindle orientation, indicating a role for Wnt signaling in cytoskeletal polarity across early blastomeres.
Conclusions:
- The MOM genes, including a Wnt pathway component, are critical for asymmetric endoderm specification in C. elegans.
- Wnt signaling, mediated by P2-derived signals, influences POP-1 levels and cytoskeletal polarity in the EMS lineage.
- This pathway impacts cell polarity in multiple blastomeres during early embryonic development.
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