| Literature DB >> 33372703 |
Qiangbo Liu1, Yanglin Ding1, Yiting Shi1, Liang Ma1, Yi Wang1, Chunpeng Song2, Katie A Wilkins3, Julia M Davies3, Heather Knight4, Marc R Knight4, Zhizhong Gong1, Yan Guo1, Shuhua Yang1.
Abstract
The transient elevation of cytosolic free calcium concentration ([Ca2+ ]cyt ) induced by cold stress is a well-established phenomenon; however, the underlying mechanism remains elusive. Here, we report that the Ca2+ -permeable transporter ANNEXIN1 (AtANN1) mediates cold-triggered Ca2+ influx and freezing tolerance in Arabidopsis thaliana. The loss of function of AtANN1 substantially impaired freezing tolerance, reducing the cold-induced [Ca2+ ]cyt increase and upregulation of the cold-responsive CBF and COR genes. Further analysis showed that the OST1/SnRK2.6 kinase interacted with and phosphorylated AtANN1, which consequently enhanced its Ca2+ transport activity, thereby potentiating Ca2+ signaling. Consistent with these results and freezing sensitivity of ost1 mutants, the cold-induced [Ca2+ ]cyt elevation in the ost1-3 mutant was reduced. Genetic analysis indicated that AtANN1 acts downstream of OST1 in responses to cold stress. Our data thus uncover a cascade linking OST1-AtANN1 to cold-induced Ca2+ signal generation, which activates the cold response and consequently enhances freezing tolerance in Arabidopsis.Entities:
Keywords: zzm321990Arabidopsiszzm321990; OST1 kinase; calcium signal; calcium-permeable transporter AtANN1; freezing tolerance
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Year: 2020 PMID: 33372703 PMCID: PMC7809786 DOI: 10.15252/embj.2020104559
Source DB: PubMed Journal: EMBO J ISSN: 0261-4189 Impact factor: 11.598