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Two Pdk1 phosphorylation sites on the plant cell death suppressor Adi3 contribute to substrate phosphorylation
Authors:Joel W Gray  Anna C Nelson Dittrich  Sixue Chen  Julian Avila  Patrick Giavalisco  Timothy P Devarenne
Institution:1. Department of Biochemistry and Biophysics, Texas A&M University, College Station, TX, 77843, USA;2. Department of Biology, Genetics Institute, Plant Molecular and Cellular Biology Program, Interdisciplinary Center for Biotechnology Research, University of Florida, Gainesville, FL 32610, USA;3. Max Planck Institute of Molecular Plant Physiology, 14476 Glom-Potsdam, Germany
Abstract:The tomato AGC kinase Adi3 is phosphorylated by Pdk1 for activation of its cell death suppression activity. The Pdk1 phosphorylation site for activation of Adi3 is at Ser539. However, there is at least one additional Pdk1 phosphorylation site on Adi3 that has an unknown function. Here we identify an Arabidopsis thaliana sequence homologue of Adi3 termed AGC1-3. Two Pdk1 phosphorylation sites were identified on AGC1-3, activation site Ser596 and Ser269, and by homology Ser212 on Adi3 was identified as a second Pdk1 phosphorylation site. While Ser212 is not required for Adi3 autophosphorylation, Ser212 was shown to be required for full phosphorylation of the Adi3 substrate Gal83.
Keywords:Adi3  AvrPto-dependent Pto-interacting protein 3  Gal83  galactose-specific gene 83  MBP  maltose binding protein  Pdk1  3-phosphoinositide dependent protein kinase 1  PCD  programmed cell death  SnRK1  Sucrose non-Fermenting-1-Related Protein Kinase 1
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