Genetic and Molecular Analysis of Suppressors of Ras Mutations

Abstract

The goal of this research is to understand the regulation of Ras-mediated signaling in C. elegans vulva! development. We describe the identification and characterization of a novel gene, sur-8, that functions to regulate a receptor tyrosine kinase-Ras-MAp kinase- mediated signal transduction pathway during C. elegans vulval development. Mutations in sur-8 were identified as suppressors of an activated let-60 ras mutation. Our genetic analysis indicates that sur% plays a positive regulatory role in Ras-mediated signaling, and appears to function downstream of Ras but not downstream of Raf. Although sur-8 mutations by themselves have no effect on normal Ras-mediated signaling, reduction of sur-8 function dramatically enhances mpk-1 MAP kinase and ksr-1 mutations and an increase of sur-8 dosage enhances an activated let- 60 ras mutation. We found that sur-8 encodes a novel protein conserved in mammals that is composed predominantly of leucine-rich repeats. SUR-8 interacts directly with LET-60 Ras, but fails to interact with a putative effector domain mutant, P34G. A structural and functional SUR-8 homologue in humans specifically binds K-Ras and N-Pas but not H-Ras in vitro. Our results indicate that sur-8 is an evolutionarily conserved positive regulator of Ras signaling pathways and that SUR-8 may mediate its effects through Ras binding. We also describe evidence that a regulatory B subunit of Protein Phosphatase 2A (pP2A) positively regulates an RTK-Ras-MAP kinase signaling cascade during Caenorhabditis elegans vulval induction. Although reduction of sur-6 PP2A-B function causes few vulva! induction defects in an otherwise wild-type background, sur-6 PP2A-B mutations suppress the Multivulva phenotype of an activated ras mutation and enhance the Vulvaless phenotype of mutations in lin-45 raf sur-8 or mpk-1.

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Document Details

Document Type
Technical Report
Publication Date
Oct 01, 1999
Accession Number
ADA383051

Entities

People

  • Derek Sieburth

Organizations

  • University of Colorado Boulder

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DTIC Thesaurus Topics

  • Amino Acids
  • Animals
  • Biology
  • Carrier Proteins
  • Cell Physiological Processes
  • Cells
  • Chemistry
  • Developmental Biology
  • Genes
  • Genetic Code
  • Genetic Structures
  • Genetically Modified Organisms
  • Genetics
  • Genome
  • Identification
  • Phenotypes
  • Proteins

Fields of Study

  • Biology

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  • Molecular and genetic basis of cancer.

Technology Areas

  • Biotechnology