| Literature DB >> 29760074 |
Kentaro Nakaminami1, Masanori Okamoto1,2, Mieko Higuchi-Takeuchi3, Takeshi Yoshizumi3, Yube Yamaguchi4, Yoichiro Fukao5, Minami Shimizu6, Chihiro Ohashi6, Maho Tanaka1, Minami Matsui7, Kazuo Shinozaki6, Motoaki Seki8,9,10,11, Kousuke Hanada12,10,13.
Abstract
Peptides encoded by small coding genes play an important role in plant development, acting in a similar manner as phytohormones. Few hormone-like peptides, however, have been shown to play a role in abiotic stress tolerance. In the current study, 17 Arabidopsis genes coding for small peptides were found to be up-regulated in response to salinity stress. To identify peptides leading salinity stress tolerance, we generated transgenic Arabidopsis plants overexpressing these small coding genes and assessed survivability and root growth under salinity stress conditions. Results indicated that 4 of the 17 overexpressed genes increased salinity stress tolerance. Further studies focused on AtPROPEP3, which was the most highly up-regulated gene under salinity stress. Treatment of plants with synthetic peptides encoded by AtPROPEP3 revealed that a C-terminal peptide fragment (AtPep3) inhibited the salt-induced bleaching of chlorophyll in seedlings. Conversely, knockdown AtPROPEP3 transgenic plants exhibited a hypersensitive phenotype under salinity stress, which was complemented by the AtPep3 peptide. This functional AtPep3 peptide region overlaps with an AtPep3 elicitor peptide that is related to the immune response of plants. Functional analyses with a receptor mutant of AtPep3 revealed that AtPep3 was recognized by the PEPR1 receptor and that it functions to increase salinity stress tolerance in plants. Collectively, these data indicate that AtPep3 plays a significant role in both salinity stress tolerance and immune response in Arabidopsis.Entities:
Keywords: Arabidopsis; abiotic stress; peptide hormone; salt tolerance; small coding gene
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Year: 2018 PMID: 29760074 PMCID: PMC5984501 DOI: 10.1073/pnas.1719491115
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205