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 vulval 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-8 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-J 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-Ras 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.
Document Details
- Document Type
- Technical Report
- Publication Date
- Oct 01, 1998
- Accession Number
- ADA377814
Entities
People
- Derek Sieburth
Organizations
- University of Colorado Boulder