The STE20/germinal center kinase POD6 interacts with the NDR kinase COT1 and is involved in polar tip extension in Neurospora crassa

Mol Biol Cell. 2006 Sep;17(9):4080-92. doi: 10.1091/mbc.e06-01-0072. Epub 2006 Jul 5.

Abstract

Members of the Ste20 and NDR protein kinase families are important for normal cell differentiation and morphogenesis in various organisms. We characterized POD6 (NCU02537.2), a novel member of the GCK family of Ste20 kinases that is essential for hyphal tip extension and coordinated branch formation in the filamentous fungus Neurospora crassa. pod-6 and the NDR kinase mutant cot-1 exhibit indistinguishable growth defects, characterized by cessation of cell elongation, hyperbranching, and altered cell-wall composition. We suggest that POD6 and COT1 act in the same genetic pathway, based on the fact that both pod-6 and cot-1 can be suppressed by 1) environmental stresses, 2) altering protein kinase A activity, and 3) common extragenic suppressors (ropy, as well as gul-1, which is characterized here as the ortholog of the budding and fission yeasts SSD1 and Sts5, respectively). Unlinked noncomplementation of cot-1/pod-6 alleles indicates a potential physical interaction between the two kinases, which is further supported by coimmunoprecipitation analyses, partial colocalization of both proteins in wild-type cells, and their common mislocalization in dynein/kinesin mutants. We conclude that POD6 acts together with COT1 and is essential for polar cell extension in a kinesin/dynein-dependent manner in N. crassa.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Catalytic Domain
  • Cell Polarity* / drug effects
  • Cyclic AMP-Dependent Protein Kinases / antagonists & inhibitors
  • Fungal Proteins / metabolism*
  • Germinal Center Kinases
  • Hyphae / cytology
  • Microtubules / metabolism
  • Molecular Motor Proteins / metabolism
  • Molecular Sequence Data
  • Mutation / drug effects
  • Mutation / genetics
  • Neurospora crassa / cytology*
  • Neurospora crassa / drug effects
  • Neurospora crassa / enzymology*
  • Phenotype
  • Protein Binding / drug effects
  • Protein Serine-Threonine Kinases / chemistry
  • Protein Serine-Threonine Kinases / metabolism*
  • Protein Transport / drug effects
  • Sequence Alignment
  • Sodium Chloride / pharmacology

Substances

  • Fungal Proteins
  • Germinal Center Kinases
  • Molecular Motor Proteins
  • Sodium Chloride
  • Protein Serine-Threonine Kinases
  • Cyclic AMP-Dependent Protein Kinases

Associated data

  • GENBANK/DQ336953