Arabidopsis PIAL1 and 2 Promote SUMO Chain Formation as E4-Type SUMO Ligases and Are Involved in Stress Responses and Sulfur Metabolism
Author(s) -
Konstantin Tomanov,
Anja Zeschmann,
Rebecca Hermkes,
Karolin Eifler,
Ionida Ziba,
Michele Grieco,
Maria Novatchkova,
Kay Hofmann,
H. Hesse,
Andreas Bachmair
Publication year - 2014
Publication title -
the plant cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.324
H-Index - 341
eISSN - 1532-298X
pISSN - 1040-4651
DOI - 10.1105/tpc.114.131300
Subject(s) - sumo protein , sumo enzymes , ubiquitin , arabidopsis , mutant , biochemistry , ubiquitin ligase , arabidopsis thaliana , proteolysis , ubiquitin protein ligases , biology , microbiology and biotechnology , enzyme , chemistry , gene
The Arabidopsis thaliana genes PROTEIN INHIBITOR OF ACTIVATED STAT LIKE1 (PIAL1) and PIAL2 encode proteins with SP-RING domains, which occur in many ligases of the small ubiquitin-related modifier (SUMO) conjugation pathway. We show that PIAL1 and PIAL2 function as SUMO ligases capable of SUMO chain formation and require the SUMO-modified SUMO-conjugating enzyme SCE1 for optimal activity. Mutant analysis indicates a role for PIAL1 and 2 in salt stress and osmotic stress responses, whereas under standard conditions, the mutants show close to normal growth. Mutations in PIAL1 and 2 also lead to altered sulfur metabolism. We propose that, together with SUMO chain binding ubiquitin ligases, these enzymes establish a pathway for proteolytic removal of sumoylation substrates.
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