TY - JOUR
T1 - PCH1 regulates light, temperature, and circadian signaling as a structural component of phytochrome B-photobodies in Arabidopsis
AU - Huang, He
AU - McLoughlin, Katrice E.
AU - Sorkin, Maria L.
AU - Sethe Burgie, E.
AU - Bindbeutel, Rebecca K.
AU - Vierstra, Richard D.
AU - Nusinow, Dmitri A.
N1 - Funding Information:
ACKNOWLEDGMENTS. We thank Dr. Margaret E. Wilson for critically reading the manuscript and Jeffery Allen for technical assistance. The US National Science Foundation (NSF) funded the acquisition of a Leica SP8-X confocal microscope (Grant DBI-1337680). D.A.N. was supported by NSF IOS Award 1456796, and M.L.S. was supported by NSF Division of Graduate Education Award 1745038. The R.D.V. lab was supported by grants from the NSF’s Molecular Biophysics Program (MCB-1329956) and National Institutes of Health (R01 GM127892-01A1, to R.D.V.).
Funding Information:
We thank Dr. Margaret E. Wilson for critically reading the manuscript and Jeffery Allen for technical assistance. The US National Science Foundation (NSF) funded the acquisition of a Leica SP8-X confocal microscope (Grant DBI-1337680). D.A.N. was supported by NSF IOS Award 1456796, and M.L.S. was supported by NSF Division of Graduate Education Award 1745038. The R.D.V. lab was supported by grants from the NSF’s Molecular Biophysics Program (MCB-1329956) and National Institutes of Health (R01 GM127892-01A1, to R.D.V.).
Publisher Copyright:
© 2019 National Academy of Sciences. All rights reserved.
PY - 2019
Y1 - 2019
N2 - The members of the phytochrome (phy) family of bilin-containing photoreceptors are major regulators of plant photomorphogenesis through their unique ability to photointerconvert between a biologically inactive red light-absorbing Pr state and an active far-red light-absorbing Pfr state. While the initial steps in Pfr signaling are unclear, an early event for the phyB isoform after photoconversion is its redistribution from the cytoplasm into subnuclear foci known as photobodies (PBs), which dissipate after Pfr reverts back to Pr by far-red irradiation or by temperature-dependent nonphotochemical reversion. Here we present evidence that PHOTOPERIODIC CONTROL OF HYPOCOTYL 1 (PCH1) functions both as an essential structural component of phyB-containing PBs and as a direct regulator of thermal reversion that is sufficient to stabilize phyB as Pfr in vitro. By examining the genetic interaction between a constitutively active phyBY276H-YFP allele (YHB-YFP) and PCH1, we show that the loss of PCH1 prevents YHB from coalescing into PBs without affecting its nuclear localization, whereas overexpression of PCH1 dramatically increases PB levels. Loss of PCH1, presumably by impacting phyB-PB assembly, compromises a number of events elicited in YHB-YFP plants, including their constitutive photomorphogenic phenotype, red light-regulated thermomorphogenesis, and input of phyB into the circadian clock. Conversely, elevated levels of both phyB and PCH1 generate stable, yet far-red light–reversible PBs that persisted for days. Collectively, our data demonstrate that the assembly of PCH1-containing PBs is critical for phyB signaling to multiple outputs and suggest that altering PB dynamics could be exploited to modulate plant responses to light and temperature.
AB - The members of the phytochrome (phy) family of bilin-containing photoreceptors are major regulators of plant photomorphogenesis through their unique ability to photointerconvert between a biologically inactive red light-absorbing Pr state and an active far-red light-absorbing Pfr state. While the initial steps in Pfr signaling are unclear, an early event for the phyB isoform after photoconversion is its redistribution from the cytoplasm into subnuclear foci known as photobodies (PBs), which dissipate after Pfr reverts back to Pr by far-red irradiation or by temperature-dependent nonphotochemical reversion. Here we present evidence that PHOTOPERIODIC CONTROL OF HYPOCOTYL 1 (PCH1) functions both as an essential structural component of phyB-containing PBs and as a direct regulator of thermal reversion that is sufficient to stabilize phyB as Pfr in vitro. By examining the genetic interaction between a constitutively active phyBY276H-YFP allele (YHB-YFP) and PCH1, we show that the loss of PCH1 prevents YHB from coalescing into PBs without affecting its nuclear localization, whereas overexpression of PCH1 dramatically increases PB levels. Loss of PCH1, presumably by impacting phyB-PB assembly, compromises a number of events elicited in YHB-YFP plants, including their constitutive photomorphogenic phenotype, red light-regulated thermomorphogenesis, and input of phyB into the circadian clock. Conversely, elevated levels of both phyB and PCH1 generate stable, yet far-red light–reversible PBs that persisted for days. Collectively, our data demonstrate that the assembly of PCH1-containing PBs is critical for phyB signaling to multiple outputs and suggest that altering PB dynamics could be exploited to modulate plant responses to light and temperature.
KW - Circadian clock
KW - Photobodies
KW - Photomorphogenesis
KW - Phytochrome
KW - Thermomorphogenesis
UR - http://www.scopus.com/inward/record.url?scp=85065198467&partnerID=8YFLogxK
U2 - 10.1073/pnas.1818217116
DO - 10.1073/pnas.1818217116
M3 - Article
C2 - 30948632
AN - SCOPUS:85065198467
SN - 0027-8424
VL - 116
SP - 8603
EP - 8608
JO - Proceedings of the National Academy of Sciences of the United States of America
JF - Proceedings of the National Academy of Sciences of the United States of America
IS - 17
ER -