Abstract
During C. elegans development, Wnt/WG signaling is required for differences in cell fate between sister cells born from anterior/posterior divisions. A beta-catenin-related gene, wrm-1, and the lit-1 gene are effectors of this signaling pathway and appear to downregulate the activity of POP-1, a TCF/LEF-related protein, in posterior daughter cells. We show here that lit-1 encodes a serine/threonine protein kinase homolog related to the Drosophila tissue polarity protein Nemo. We demonstrate that the WRM-1 protein binds to LIT-1 in vivo and that WRM-1 can activate the LIT-1 protein kinase when coexpressed in vertebrate tissue culture cells. This activation leads to phosphorylation of POP-1 and to apparent changes in its subcellular localization. Our findings provide evidence for novel regulatory avenues for an evolutionarily conserved Wnt/WG signaling pathway.
Publication types
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Research Support, Non-U.S. Gov't
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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Amino Acid Sequence
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Animals
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COS Cells
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Caenorhabditis elegans / genetics
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Caenorhabditis elegans / metabolism
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Caenorhabditis elegans Proteins*
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Cytoskeletal Proteins / genetics
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Cytoskeletal Proteins / metabolism*
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DNA-Binding Proteins / metabolism
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Enzyme Activation
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Helminth Proteins / genetics
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Helminth Proteins / metabolism*
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High Mobility Group Proteins / metabolism
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Membrane Proteins / genetics
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Membrane Proteins / metabolism*
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Mitogen-Activated Protein Kinases*
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Molecular Sequence Data
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Phosphorylation
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Protein Serine-Threonine Kinases / genetics
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Protein Serine-Threonine Kinases / metabolism
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Signal Transduction*
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Trans-Activators*
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beta Catenin
Substances
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Caenorhabditis elegans Proteins
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Cytoskeletal Proteins
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DNA-Binding Proteins
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Helminth Proteins
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High Mobility Group Proteins
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Membrane Proteins
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Mom-5 protein, C elegans
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Trans-Activators
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WRM-1 protein, C elegans
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beta Catenin
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pop-1 protein, C elegans
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Protein Serine-Threonine Kinases
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lit-1 protein, C elegans
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Mitogen-Activated Protein Kinases
Associated data
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GENBANK/AF143243
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GENBANK/AF143244