Eukaryotic Cell doi:10.1128/EC.00047-07
Copyright (c) 2007, American Society for Microbiology and/or the Listed Authors/Institutions. All Rights Reserved.
Further characterization of the signaling proteolysis step in the Aspergillus nidulans pH signal transduction pathway
María M Peñas,
América Hervás-Aguilar,
Tatiana Múnera-Huertas,
Elena Reoyo,
Miguel Á Peñalva,
Herbert N Arst Jr,
and
Joan Tilburn*
Department of Molecular Microbiology and Infection, Imperial College London, The Flowers Building, London, SW7 2AZ, United Kingdom and Departamento de Microbiología Molecular, Centro de Investigaciones Biológicas, CSIC,Ramiro de Maeztu, 9,Madrid 28040, Spain
* To whom correspondence should be addressed. Email:
j.tilburn{at}imperial.ac.uk.
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Abstract |
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The Aspergillus nidulans pH responsive transcription factor PacC is modulated by limited, two-step proteolysis. The first, pH-regulated cleavage occurs in the 24-residue highly conserved ‘signaling protease box’ in response to the alkaline pH signal. This is transduced by the Pal signaling pathway containing the predicted calpain-like cysteine protease and likely signaling protease, PalB. In this work we carried out classical mutational analysis of the putative signaling protease PalB and describe nine missense and eighteen truncating loss-of-function (including null) mutations. Mutations in the region of and affecting directly the predicted catalytic cysteine strongly support the deduction that PalB is a cysteine protease. Truncating and missense mutations affecting the C-terminus highlight the importance of this region. Analysis of HA3-tagged PalB in Western blots demonstrates that PalB levels are independent of pH and Pal signal transduction. We have followed the processing of MYC3-tagged PacC in Western blots. We show unequivocally that PalB is essential for the signaling proteolysis and is definitely not the processing protease. In addition we have substituted 15 residues of the signaling protease box of MYC3-tagged PacC (pacC900) with alanine. The majority of these substitutions are silent. Leu481Ala, Tyr493Ala, and Gln499Ala result in delayed PacC processing in response to shifting from acidic to alkaline medium as determined by Western blot analysis. Leu498Ala reduces function much more markedly as determined by plate tests and processing recalcitrance. Excepting Leu498, this demonstrates that PacC signaling proteolysis is largely independent of sequence in the cleavage region.
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