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Os MADS 57 together with Os TB 1 coordinates transcription of its target Os WRKY 94 and D14 to switch its organogenesis to defense for cold adaptation in rice
Author(s) -
Chen Liping,
Zhao Yuan,
Xu Shujuan,
Zhang Zeyong,
Xu Yunyuan,
Zhang Jingyu,
Chong Kang
Publication year - 2018
Publication title -
new phytologist
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.742
H-Index - 244
eISSN - 1469-8137
pISSN - 0028-646X
DOI - 10.1111/nph.14977
Subject(s) - wrky protein domain , organogenesis , transcription factor , biology , microbiology and biotechnology , gene , genetics , transcriptome , gene expression
Summary Plants modify their development to adapt to their environment, protecting themselves from detrimental conditions such as chilling stress by triggering a variety of signaling pathways; however, little is known about how plants coordinate developmental patterns and stress responses at the molecular level. Here, we demonstrate that interacting transcription factors Os MADS 57 and Os TB 1 directly target the defense gene Os WRKY 94 and the organogenesis gene D14 to trade off the functions controlling/moderating rice tolerance to cold. Overexpression of Os MADS 57 maintains rice tiller growth under chilling stress. Os MADS 57 binds directly to the promoter of Os WRKY 94 , activating its transcription for the cold stress response, while suppressing its activity under normal temperatures. In addition, Os WRKY 94 was directly targeted and suppressed by Os TB 1 under both normal and chilling temperatures. However, D14 transcription was directly promoted by Os MADS 57 for suppressing tillering under the chilling treatment, whereas D14 was repressed for enhancing tillering under normal condition.We demonstrated that Os MADS 57 and Os TB 1 conversely affect rice chilling tolerance via targeting Os WRKY 94 . Our findings highlight a molecular genetic mechanism coordinating organogenesis and chilling tolerance in rice, which supports and extends recent work suggesting that chilling stress environments influence organ differentiation.