Details

Autor(en) / Beteiligte

• Albrecht, Verónica
• Ritz, Olga
• Linder, Sabine
• Harter, Klaus
• Kudla, Jörg

Titel

The NAF domain defines a novel protein-protein interaction module conserved in Ca2+-regulated kinases

Ist Teil von

• The EMBO journal, 2001-03, Vol.20 (5), p.1051-1063

Ort / Verlag

Chichester, UK: John Wiley & Sons, Ltd

Erscheinungsjahr

2001

Link zum Volltext

Quelle

Wiley Online Library Journals Frontfile Complete

Beschreibungen/Notizen

• The Arabidopsis calcineurin B‐like calcium sensor proteins (AtCBLs) interact with a group of serine‐threonine protein kinases (AtCIPKs) in a calcium‐dependent manner. Here we identify a 24 amino acid domain (NAF domain) unique to these kinases as being required and sufficient for interaction with all known AtCBLs. Mutation of conserved residues either abolished or significantly diminished the affinity of AtCIPK1 for AtCBL2. Comprehensive two‐hybrid screens with various AtCBLs identified 15 CIPKs as potential targets of CBL proteins. Database analyses revealed additional kinases from Arabidopsis and other plant species harbouring the NAF interaction module. Several of these kinases have been implicated in various signalling pathways mediating responses to stress, hormones and environmental cues. Full‐length CIPKs show preferential interaction with distinct CBLs in yeast and in vitro assays. Our findings suggest differential interaction affinity as one of the mechanisms generating the temporal and spatial specificity of calcium signals within plant cells and that different combinations of CBL–CIPK proteins contribute to the complex network that connects various extracellular signals to defined cellular responses.