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Cdc42p-interacting protein Bem4p regulates the filamentous-growth mitogen-activated protein kinase pathway

  • Andrew Pitoniak
  • , Colin A. Chavel
  • , Jacky Chow
  • , Jeremy Smith
  • , Diawoye Camara
  • , Sheelarani Karunanithi
  • , Boyang Li
  • , Kennith H. Wolfe
  • , Paul J. Cullen
  • SUNY Buffalo
  • University College Dublin

Research output: Contribution to journalArticlepeer-review

18 Scopus citations

Abstract

The ubiquitous Rho (Ras homology) GTPase Cdc42p can function in different settings to regulate cell polarity and cellular signaling. How Cdc42p and other proteins are directed to function in a particular context remains unclear. We show that the Cdc42p-interacting protein Bem4p regulates the mitogen-activated protein kinase (MAPK) pathway that controls filamentous growth in Saccharomyces cerevisiae. Bem4p controlled the filamentous-growth pathway but not other MAPK pathways (mating or high-osmolarity glycerol response [HOG]) that also require Cdc42p and other shared components. Bem4p associated with the plasma membrane (PM) protein, Sho1p, to regulate MAPK activity and cell polarization under nutrient-limiting conditions that favor filamentous growth. Bem4p also interacted with the major activator of Cdc42p, the guanine nucleotide exchange factor (GEF) Cdc24p, which we show also regulates the filamentous-growth pathway. Bem4p interacted with the pleckstrin homology (PH) domain of Cdc24p, which functions in an autoinhibitory capacity, and was required, along with other pathway regulators, to maintain Cdc24p at polarized sites during filamentous growth. Bem4p also interacted with the MAPK kinase kinase (MAPKKK) Ste11p. Thus, Bem4p is a new regulator of the filamentous-growth MAPK pathway and binds to general proteins, like Cdc42p and Ste11p, to promote a pathway-specific response.

Original languageEnglish
Pages (from-to)417-436
Number of pages20
JournalMolecular and Cellular Biology
Volume35
Issue number2
DOIs
StatePublished - 2015

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