Literature DB >> 9671465

Caenorhabditis elegans SUR-5, a novel but conserved protein, negatively regulates LET-60 Ras activity during vulval induction.

T Gu1, S Orita, M Han.   

Abstract

The let-60 ras gene acts in a signal transduction pathway to control vulval differentiation in Caenorhabditis elegans. By screening suppressors of a dominant negative let-60 ras allele, we isolated three loss-of-function mutations in the sur-5 gene which appear to act as negative regulators of let-60 ras during vulval induction. sur-5 mutations do not cause an obvious mutant phenotype of their own, and they appear to specifically suppress only one of the two groups of let-60 ras dominant negative mutations, suggesting that the gene may be involved in a specific aspect of Ras activation. Consistent with its negative function, overexpressing sur-5 from an extragenic array partially suppresses the Multivulva phenotype of an activated let-60 ras mutation and causes synergistic phenotypes with a lin-45 raf mutation. We have cloned sur-5 and shown that it encodes a novel protein. We have also identified a potential mammalian SUR-5 homolog that is about 35% identical to the worm protein. SUR-5 also has some sequence similarity to acetyl coenzyme A synthetases and is predicted to contain ATP/GTP and AMP binding sites. Our results suggest that sur-5 gene function may be conserved through evolution.

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Year:  1998        PMID: 9671465      PMCID: PMC109041          DOI: 10.1128/MCB.18.8.4556

Source DB:  PubMed          Journal:  Mol Cell Biol        ISSN: 0270-7306            Impact factor:   4.272


  37 in total

1.  The putative acetyl-CoA synthetase gene of Cryptosporidium parvum and a new conserved protein motif in acetyl-CoA synthetases.

Authors:  N V Khramtsov; D S Blunt; B A Montelone; S J Upton
Journal:  J Parasitol       Date:  1996-06       Impact factor: 1.276

Review 2.  Control and integration of cell signaling pathways during C. elegans vulval development.

Authors:  M Sundaram; M Han
Journal:  Bioessays       Date:  1996-06       Impact factor: 4.345

3.  The multivulva phenotype of certain Caenorhabditis elegans mutants results from defects in two functionally redundant pathways.

Authors:  E L Ferguson; H R Horvitz
Journal:  Genetics       Date:  1989-09       Impact factor: 4.562

4.  The Caenorhabditis elegans gene lin-1 encodes an ETS-domain protein and defines a branch of the vulval induction pathway.

Authors:  G J Beitel; S Tuck; I Greenwald; H R Horvitz
Journal:  Genes Dev       Date:  1995-12-15       Impact factor: 11.361

5.  The C. elegans ksr-1 gene encodes a novel Raf-related kinase involved in Ras-mediated signal transduction.

Authors:  M Sundaram; M Han
Journal:  Cell       Date:  1995-12-15       Impact factor: 41.582

6.  The ksr-1 gene encodes a novel protein kinase involved in Ras-mediated signaling in C. elegans.

Authors:  K Kornfeld; D B Hom; H R Horvitz
Journal:  Cell       Date:  1995-12-15       Impact factor: 41.582

7.  Identification and cloning of unc-119, a gene expressed in the Caenorhabditis elegans nervous system.

Authors:  M Maduro; D Pilgrim
Journal:  Genetics       Date:  1995-11       Impact factor: 4.562

8.  Ras farnesyltransferase inhibitors suppress the phenotype resulting from an activated ras mutation in Caenorhabditis elegans.

Authors:  M Hara; M Han
Journal:  Proc Natl Acad Sci U S A       Date:  1995-04-11       Impact factor: 11.205

9.  The lin-3/let-23 pathway mediates inductive signalling during male spicule development in Caenorhabditis elegans.

Authors:  H M Chamberlin; P W Sternberg
Journal:  Development       Date:  1994-10       Impact factor: 6.868

10.  Three genes of the MAP kinase cascade, mek-2, mpk-1/sur-1 and let-60 ras, are required for meiotic cell cycle progression in Caenorhabditis elegans.

Authors:  D L Church; K L Guan; E J Lambie
Journal:  Development       Date:  1995-08       Impact factor: 6.868

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  72 in total

1.  Demonstration of the in vivo interaction of key cell death regulators by structure-based design of second-site suppressors.

Authors:  J Parrish; H Metters; L Chen; D Xue
Journal:  Proc Natl Acad Sci U S A       Date:  2000-10-24       Impact factor: 11.205

2.  Do males facilitate the spread of novel phenotypes within populations of the androdioecious nematode Caenorhabditis elegans?

Authors:  Viktoria Wegewitz; Hinrich Schulenburg; Adrian Streit
Journal:  J Nematol       Date:  2009-09       Impact factor: 1.402

3.  Caenorhabditis elegans wsp-1 regulation of synaptic function at the neuromuscular junction.

Authors:  Yuqian Zhang; Terrance J Kubiseski
Journal:  J Biol Chem       Date:  2010-05-25       Impact factor: 5.157

Review 4.  Cancer models in Caenorhabditis elegans.

Authors:  Natalia V Kirienko; Kumaran Mani; David S Fay
Journal:  Dev Dyn       Date:  2010-05       Impact factor: 3.780

5.  A screenable in vivo assay to study proteostasis networks in Caenorhabditis elegans.

Authors:  Alexandra Segref; Serena Torres; Thorsten Hoppe
Journal:  Genetics       Date:  2011-02-01       Impact factor: 4.562

6.  A novel mechanism underlies caspase-dependent conversion of the dicer ribonuclease into a deoxyribonuclease during apoptosis.

Authors:  Xiao Ge; Xiang Zhao; Akihisa Nakagawa; Xinqi Gong; Riley Robert Skeen-Gaar; Yong Shi; Haipeng Gong; Xinquan Wang; Ding Xue
Journal:  Cell Res       Date:  2013-12-10       Impact factor: 25.617

Review 7.  Canonical RTK-Ras-ERK signaling and related alternative pathways.

Authors:  Meera V Sundaram
Journal:  WormBook       Date:  2013-07-11

8.  Modulation of KSR activity in Caenorhabditis elegans by Zn ions, PAR-1 kinase and PP2A phosphatase.

Authors:  John H Yoder; Huira Chong; Kun-Liang Guan; Min Han
Journal:  EMBO J       Date:  2003-12-11       Impact factor: 11.598

9.  The FMRFamide-related neuropeptide FLP-20 is required in the mechanosensory neurons during memory for massed training in C. elegans.

Authors:  Chris Li; Tiffany A Timbers; Jacqueline K Rose; Tahereh Bozorgmehr; Andrea McEwan; Catharine H Rankin
Journal:  Learn Mem       Date:  2013-01-16       Impact factor: 2.460

10.  The N- or C-terminal domains of DSH-2 can activate the C. elegans Wnt/beta-catenin asymmetry pathway.

Authors:  Ryan S King; Stephanie L Maiden; Nancy C Hawkins; Ambrose R Kidd; Judith Kimble; Jeff Hardin; Timothy D Walston
Journal:  Dev Biol       Date:  2009-01-23       Impact factor: 3.582

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