Your browser doesn't support javascript.
loading
Two SnRK2-Interacting Calcium Sensor Isoforms Negatively Regulate SnRK2 Activity by Different Mechanisms.
Tarnowski, Krzysztof; Klimecka, Maria; Ciesielski, Arkadiusz; Goch, Grazyna; Kulik, Anna; Fedak, Halina; Poznanski, Jaroslaw; Lichocka, Malgorzata; Pierechod, Marcin; Engh, Richard A; Dadlez, Michal; Dobrowolska, Grazyna; Bucholc, Maria.
Afiliação
  • Tarnowski K; Institute of Biochemistry and Biophysics, Polish Academy of Sciences, 02-106 Warsaw, Poland.
  • Klimecka M; Institute of Biochemistry and Biophysics, Polish Academy of Sciences, 02-106 Warsaw, Poland.
  • Ciesielski A; Institute of Biochemistry and Biophysics, Polish Academy of Sciences, 02-106 Warsaw, Poland.
  • Goch G; Warsaw University, Department of Chemistry, 02-093 Warsaw, Poland.
  • Kulik A; Institute of Biochemistry and Biophysics, Polish Academy of Sciences, 02-106 Warsaw, Poland.
  • Fedak H; Institute of Biochemistry and Biophysics, Polish Academy of Sciences, 02-106 Warsaw, Poland.
  • Poznanski J; Institute of Biochemistry and Biophysics, Polish Academy of Sciences, 02-106 Warsaw, Poland.
  • Lichocka M; Institute of Biochemistry and Biophysics, Polish Academy of Sciences, 02-106 Warsaw, Poland.
  • Pierechod M; Institute of Biochemistry and Biophysics, Polish Academy of Sciences, 02-106 Warsaw, Poland.
  • Engh RA; The Norwegian Center for Structure Biology, Institute of Chemistry, University of Tromsø, N-9037 Tromsø, Norway.
  • Dadlez M; The Norwegian Center for Structure Biology, Institute of Chemistry, University of Tromsø, N-9037 Tromsø, Norway.
  • Dobrowolska G; Institute of Biochemistry and Biophysics, Polish Academy of Sciences, 02-106 Warsaw, Poland.
  • Bucholc M; University of Warsaw, Institute of Genetics and Biotechnology, 02-106 Warsaw, Poland.
Plant Physiol ; 182(2): 1142-1160, 2020 02.
Article em En | MEDLINE | ID: mdl-31699848
ABSTRACT
SNF1-related protein kinases 2 (SnRK2s) are key signaling elements regulating abscisic acid-dependent plant development and responses to environmental stresses. Our previous data showed that the SnRK2-interacting Calcium Sensor (SCS) inhibits SnRK2 activity. Use of alternative transcription start sites located within the Arabidopsis (Arabidopsis thaliana) AtSCS gene results in two in-frame transcripts and subsequently two proteins, that differ only by the sequence position of the N terminus. We previously described the longer AtSCS-A, and now describe the shorter AtSCS-B and compare the two isoforms. The two isoforms differ substantially in their expression profiles in plant organs and in response to environmental stresses, in their calcium binding properties, and in their conformational dynamics in the presence and absence of Ca2+ Only AtSCS-A has the features of a calcium sensor. Both forms inhibit SnRK2 activity, but while AtSCS-A requires calcium for inhibition, AtSCS-B does not. Analysis of Arabidopsis plants stably expressing 35SAtSCS-A-c-myc or 35SAtSCS-B-c-myc in the scs-1 knockout mutant background revealed that, in planta, both forms are negative regulators of abscisic acid-induced SnRK2 activity and regulate plant resistance against water deficit. Moreover, the data highlight biochemical, biophysical, and functional properties of EF-hand-like motifs in plant proteins.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Estresse Fisiológico / Cálcio / Proteínas Serina-Treonina Quinases / Arabidopsis / Proteínas de Arabidopsis / Estresse Salino Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Estresse Fisiológico / Cálcio / Proteínas Serina-Treonina Quinases / Arabidopsis / Proteínas de Arabidopsis / Estresse Salino Idioma: En Ano de publicação: 2020 Tipo de documento: Article