Abstract
The Caenorhabditis elegans lin-12 and glp-1 genes encode members of the LIN-12/NOTCH family of receptors. The sel-1 gene was identified as an extragenic suppressor of a lin-12 hypomorphic mutant. We show in this report that the sel-1 null phenotype is wild type, except for an apparent elevation in lin-12 and glp-1 activity in sensitized genetic backgrounds, and that this genetic interaction seems to be lin-12 and glp-1 specific. We also find that sel-1 encodes a predicted extracellular protein, with a domain sharing sequence similarity to predicted proteins from humans and yeast. SEL-1 may interact with the LIN-12 and GLP-1 receptors and/or their respective ligands to down-regulate signaling.
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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Alleles
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Amino Acid Sequence
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Animals
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Base Sequence
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Caenorhabditis elegans / genetics*
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Caenorhabditis elegans / physiology
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Caenorhabditis elegans Proteins*
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Cloning, Molecular
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DNA Primers
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Gene Expression Regulation
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Genes, Helminth*
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Genes, Regulator*
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Genotype
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Helminth Proteins / biosynthesis*
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Helminth Proteins / genetics*
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Membrane Glycoproteins / biosynthesis*
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Membrane Glycoproteins / genetics
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Membrane Proteins / biosynthesis*
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Membrane Proteins / genetics*
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Models, Genetic
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Molecular Sequence Data
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Mutagenesis
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Operon
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Polymerase Chain Reaction
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Receptors, Notch
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Restriction Mapping
Substances
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Caenorhabditis elegans Proteins
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DNA Primers
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Glp-1 protein, C elegans
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Helminth Proteins
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Lin-12 protein, C elegans
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Membrane Glycoproteins
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Membrane Proteins
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Receptors, Notch
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SEL-1 protein, C elegans
Associated data
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GENBANK/U50828
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GENBANK/U50829