TIME FOR COFFEE regulates phytochrome A-mediated hypocotyl growth through dawn-phased signaling
Author(s) -
Yan Wang,
Chen Su,
Y. Yu,
Yuqing He,
Hua Wei,
Na Li,
Hong Li,
Jie Duan,
Bin Li,
Jigang Li,
Seth J Davis,
Lei Wang
Publication year - 2022
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 - 10.1093/plcell/koac138
Subject(s) - phytochrome , biology , phytochrome a , microbiology and biotechnology , circadian clock , arabidopsis , hypocotyl , mutant , repressor , arabidopsis thaliana , cryptochrome , regulator , psychological repression , genetics , gene expression , botany , gene , red light
To enhance plant fitness under natural conditions, the circadian clock is synchronized and entrained by light via photoreceptors. In turn, the circadian clock exquisitely regulates the abundance and activity of photoreceptors via largely uncharacterized mechanisms. Here we show that the clock regulator TIME FOR COFFEE (TIC) controls the activity of the far-red light photoreceptor phytochrome A (phyA) at multiple levels in Arabidopsis thaliana. Null mutants of TIC displayed dramatically increased sensitivity to light irradiation with respect to hypocotyl growth, especially to far-red light. RNA-sequencing demonstrated that TIC and phyA play largely opposing roles in controlling light-regulated gene expression at dawn. Additionally, TIC physically interacts with the transcriptional repressor TOPLESS (TPL), which was associated with the significantly increased PHYA transcript levels in the tic-2 and tpl-1 mutants. Moreover, TIC interacts with phyA in the nucleus, thereby affecting phyA protein turnover and the formation of phyA nuclear speckles following light irradiation. Genetically, phyA was found to act downstream of TIC in regulating far red light-inhibited growth. Taken together, these findings indicate that TIC acts as a major negative regulator of phyA by integrating transcriptional and post-translational mechanisms at multiple levels.
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