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  PKA and MAPK phosphorylation of Prf1 allows promoter discrimination in Ustilago maydis.

Kaffarnik, F., Mueller, P., Leibundgut, M., Kahmann, R., & Feldbruegge, M. (2003). PKA and MAPK phosphorylation of Prf1 allows promoter discrimination in Ustilago maydis. The EMBO Journal, 22(21), 5817-5826. doi:10.1093/emboj/cdg554.

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 Creators:
Kaffarnik, Florian1, Author           
Mueller, Philip1, Author           
Leibundgut, Marc, Author
Kahmann, Regine2, Author           
Feldbruegge, Michael1, Author           
Affiliations:
1Department of Organismic Interactions, Alumni, Max Planck Institute for Terrestrial Microbiology, Max Planck Society, ou_3266313              
2Emeriti Molecular Phytopathology, Max Planck Institute for Terrestrial Microbiology, Max Planck Society, ou_3266291              

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 Abstract: Mating in Ustilago maydis requires cross-talk between cAMP and mitogen-activated protein kinase (MAPK) signalling. During this process, pheromone response factor 1 (Prf1) activates transcription of a and b mating type genes by binding to pheromone response elements (PREs) located in regulatory regions of these genes. Here, we show that PREs are also necessary and sufficient to mediate cAMP-induced gene expression. Prf1 interacts with cAMP-dependent protein kinase A (PKA) Adr1 as well as MAPK Kpp2 in vivo, and its central phosphorylation sites that are functionally important are modified by the respective kinases in vitro. PKA sites in Prf1 are essential for induced expression of a and b mating type genes. In contrast, MAPK sites are not required for pheromone-induced expression of a genes but are crucial for pheromone-responsive b gene expression. This illustrates how a single transcription factor can integrate signals from two pathways and how its phosphorylation status can determine different transcriptional responses.

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Language(s): eng - English
 Dates: 2003-10
 Publication Status: Issued
 Pages: -
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 Table of Contents: -
 Rev. Type: Peer
 Identifiers: eDoc: 50877
DOI: 10.1093/emboj/cdg554
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Title: The EMBO Journal
  Alternative Title : Embo J.
Source Genre: Journal
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Pages: - Volume / Issue: 22 (21) Sequence Number: - Start / End Page: 5817 - 5826 Identifier: -