TY - JOUR
T1 - Central clock components modulate plant shade avoidance by directly repressing transcriptional activation activity of PIF proteins
AU - Zhang, Yu
AU - Pfeiffer, Anne
AU - Tepperman, James M.
AU - Dalton-Roesler, Jutta
AU - Leivar, Pablo
AU - Grandio, Eduardo Gonzalez
AU - Quail, Peter H.
N1 - Funding Information:
ACKNOWLEDGMENTS. We thank Ken S. Heyndrickx and Klaas Vandepoele for sharing genomic datasets of their 25 TFs and providing analytical support; David Somers, Eva Farre, Norihito Nakamichi, and Takeshi Mizuno for sharing plant materials; and Hongquan Yang and Wenxiu Wang for sharing BiFC constructs. This work was supported by NIH Grant 5R01GM047475-24 and US Department of Agriculture Agricultural Research Service Current Research Information System Grant 2030-21000-051-00D (to P.H.Q.).
Publisher Copyright:
© 2020 National Academy of Sciences. All rights reserved.
PY - 2020/2/11
Y1 - 2020/2/11
N2 - Light-environment signals, sensed by plant phytochrome photoreceptors, are transduced to target genes through direct regulation of PHYTOCHROME-INTERACTING FACTOR (PIF) transcription factor abundance and activity. Previous genome-wide DNA-binding and expression analysis has identified a set of genes that are direct targets of PIF transcriptional regulation. However, quantitative analysis of promoter occupancy versus expression level has suggested that unknown “trans factors” modulate the intrinsic transcriptional activation activity of DNA-bound PIF proteins. Here, using computational analysis of published data, we have identified PSEUDO-RESPONSE REGULATORS (PRR5 and PRR7) as displaying a high frequency of colocalization with the PIF proteins at their binding sites in the promoters of PIF Direct Target Genes (DTGs). We show that the PRRs function to suppress PIF-stimulated growth in the light and vegetative shade and that they repress the rapid PIF-induced expression of PIF-DTGs triggered by exposure to shade. The repressive action of the PRRs on both growth and DTG expression requires the PIFs, indicating direct action on PIF activity, rather than a parallel antagonistic pathway. Protein interaction assays indicate that the PRRs exert their repressive activity by binding directly to the PIF proteins in the nucleus. These findings support the conclusion that the PRRs function as direct outputs from the core circadian oscillator to regulate the expression of PIF-DTGs through modulation of PIF transcriptional activation activity, thus expanding the roles of the multifunctional PIF-signaling hub.
AB - Light-environment signals, sensed by plant phytochrome photoreceptors, are transduced to target genes through direct regulation of PHYTOCHROME-INTERACTING FACTOR (PIF) transcription factor abundance and activity. Previous genome-wide DNA-binding and expression analysis has identified a set of genes that are direct targets of PIF transcriptional regulation. However, quantitative analysis of promoter occupancy versus expression level has suggested that unknown “trans factors” modulate the intrinsic transcriptional activation activity of DNA-bound PIF proteins. Here, using computational analysis of published data, we have identified PSEUDO-RESPONSE REGULATORS (PRR5 and PRR7) as displaying a high frequency of colocalization with the PIF proteins at their binding sites in the promoters of PIF Direct Target Genes (DTGs). We show that the PRRs function to suppress PIF-stimulated growth in the light and vegetative shade and that they repress the rapid PIF-induced expression of PIF-DTGs triggered by exposure to shade. The repressive action of the PRRs on both growth and DTG expression requires the PIFs, indicating direct action on PIF activity, rather than a parallel antagonistic pathway. Protein interaction assays indicate that the PRRs exert their repressive activity by binding directly to the PIF proteins in the nucleus. These findings support the conclusion that the PRRs function as direct outputs from the core circadian oscillator to regulate the expression of PIF-DTGs through modulation of PIF transcriptional activation activity, thus expanding the roles of the multifunctional PIF-signaling hub.
KW - Gene expression regulation
KW - PIF proteins
KW - PRR proteins
KW - Phytochrome
KW - Shade avoidance
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UR - https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=pure_univeritat_ramon_llull&SrcAuth=WosAPI&KeyUT=WOS:000513898000070&DestLinkType=FullRecord&DestApp=WOS_CPL
U2 - 10.1073/pnas.1918317117
DO - 10.1073/pnas.1918317117
M3 - Article
C2 - 31988133
AN - SCOPUS:85079320907
SN - 0027-8424
VL - 117
SP - 3261
EP - 3269
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 - 6
ER -