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PMID: 7982579 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

The Caenorhabditis elegans locus lin-15, a negative regulator of a tyrosine kinase signaling pathway, encodes two different proteins.

Genetics ·Vol. 137 ·No. 4 ·1994-08-00 ·Pages 987-97

Clark SG, Lu X, Horvitz HR

Abstract

The Caenorhabditis elegans locus lin-15 negatively regulates an intercellular signaling process that induces formation of the hermaphrodite vulva. The lin-15 locus controls two separate genetic activities. Mutants that lack both activities have multiple, ectopic pseudo-vulvae resulting from the overproduction of vulval cells, whereas mutants defective in only one lin-15 activity appear wild-type. lin-15 acts non-cell-autonomously to prevent the activation of a receptor tyrosine kinase/ras signaling pathway. We report here the molecular characterization of the lin-15 locus. The two lin-15 activities are encoded by contiguous genomic regions and by two distinct, non-overlapping transcripts that may be processed from a single mRNA precursor by trans-splicing. Based on the DNA sequence, the 719- and 1,440-amino acid lin-15 proteins are not similar to each other or to known proteins. lin-15 multivulva mutants, which are defective in both lin-15 activities, contain deletions and insertions that affect the lin-15 genomic region.

Related Genes
MeSH Terms
Amino Acid Sequence Animals Base Sequence Caenorhabditis elegans/genetics,ultrastructure Caenorhabditis elegans Proteins DNA, Complementary/genetics Female Helminth Proteins/genetics,physiology Molecular Sequence Data Morphogenesis Polymorphism, Genetic Receptor Protein-Tyrosine Kinases/physiology Signal Transduction Transcription Factors/genetics,physiology Vulva/ultrastructure
Chemicals
Caenorhabditis elegans Proteins DNA, Complementary Helminth Proteins Transcription Factors lin-15A protein, C elegans lin-15B protein, C elegans Receptor Protein-Tyrosine Kinases
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Clark S G
Howard Hughes Medical Institute, Department of Biology, Massachusetts Institute of Technology, Cambridge 02139.
Lu X
Horvitz H R
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Article Info
Journal
Genetics
Abbr.
Genetics
ISSN
0016-6731
Published
1994-08-00
Pages
987-97
Language
English
Region
United States
NLM ID
0374636
PMCID
PMC1206075
Subset
IM
Grants
NIGMS NIH HHS · GM24663 · United States
NIGMS NIH HHS · GM24943 · United States
Databases
GENBANK
U10411, U10412, U10413
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