| Literature DB >> 26147561 |
Christelle Dutilleul1, Iliana Ribeiro1, Nathalie Blanc1, Cynthia D Nezames2, Xing Wang Deng2, Piotr Zglobicki3, Ana María Palacio Barrera4, Lucia Atehortùa4, Martine Courtois1, Valérie Labas5, Nathalie Giglioli-Guivarc'h1, Eric Ducos1.
Abstract
The tagging-via-substrate approach designed for the capture of mammal prenylated proteins was adapted to Arabidopsis cell culture. In this way, proteins are in vivo tagged with an azide-modified farnesyl moiety and captured thanks to biotin alkyne Click-iT® chemistry with further streptavidin-affinity chromatography. Mass spectrometry analyses identified four small GTPases and ASG2 (ALTERED SEED GERMINATION 2), a protein previously associated to the seed germination gene network. ASG2 is a conserved protein in plants and displays a unique feature that associates WD40 domains and tetratricopeptide repeats. Additionally, we show that ASG2 has a C-terminal CaaX-box that is farnesylated in vitro. Protoplast transfections using CaaX prenyltransferase mutants show that farnesylation provokes ASG2 nucleus exclusion. Moreover, ASG2 interacts with DDB1 (DAMAGE DNA BINDING protein 1), and the subcellular localization of this complex depends on ASG2 farnesylation status. Finally, germination and root elongation experiments reveal that asg2 and the farnesyltransferase mutant era1 (ENHANCED RESPONSE TO ABSCISIC ACID (ABA) 1) behave in similar manners when exposed to ABA or salt stress. To our knowledge, ASG2 is the first farnesylated DWD (DDB1 binding WD40) protein related to ABA response in Arabidopsis that may be linked to era1 phenotypes.Entities:
Keywords: ABA signalling; DDB1 CUL4 E3 ubiquitin ligase; protein farnesylation; tagging-via-substrate
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Year: 2015 PMID: 26147561 DOI: 10.1111/pce.12605
Source DB: PubMed Journal: Plant Cell Environ ISSN: 0140-7791 Impact factor: 7.228