TY - JOUR
T1 - Casein kinase 1 family regulates PRR5 and TOC1 in the Arabidopsis circadian clock
AU - Uehara, Takahiro N.
AU - Mizutani, Yoshiyuki
AU - Kuwata, Keiko
AU - Hirota, Tsuyoshi
AU - Sato, Ayato
AU - Mizoi, Junya
AU - Takao, Saori
AU - Matsuo, Hiromi
AU - Suzuki, Takamasa
AU - Ito, Shogo
AU - Saito, Ami N.
AU - Nishiwaki-Ohkawa, Taeko
AU - Yamaguchi-Shinozaki, Kazuko
AU - Yoshimura, Takashi
AU - Kay, Steve A.
AU - Itami, Kenichiro
AU - Kinoshita, Toshinori
AU - Yamaguchi, Junichiro
AU - Nakamichi, Norihito
N1 - Funding Information:
ACKNOWLEDGMENTS. We thank Y. Machida for providing pYU501, Y. Tsuchiya and K. Miwa for technical advice, and I. Yamanaka and N. Ono for technical assistance. This study was supported partly by an Institute of Transformative Bio-Molecules research award (to T.N.U., S.T., J.Y., and N.N.); Grant-in-Aid for Scientific Research on Innovative Areas 16H01140 (to J.Y.), 15H05960 (to K.Y.-S.), and 15H05956 (to T.K., K.K., and N.N.); The Naito Foundation (J.Y.); a Research Program of Arid Land Research Center of Tottori University 28D2001; the Toyoake Foundation; Japan Society for the Promotion of Science Grants-in-Aid for Scientific Research 17K19229 and 18H02136; and a JST Precursory Research for Embryonic Science and Technology Grant JPMJPR11B9 (to N.N.). Institute of Transformative Bio-Molecules is supported by the World Premier International Research Center Initiative, Japan.
Funding Information:
We thank Y. Machida for providing pYU501, Y. Tsuchiya and K. Miwa for technical advice, and I. Yamanaka and N. Ono for technical assistance. This study was supported partly by an Institute of Transformative Bio-Molecules research award (to T.N.U., S.T., J.Y., and N.N.); Grant-in-Aid for Scientific Research on Innovative Areas 16H01140 (to J.Y.), 15H05960 (to K.Y.-S.), and 15H05956 (to T.K., K.K., and N.N.); The Naito Foundation (J.Y.); a Research Program of Arid Land Research Center of Tottori University 28D2001; the Toyoake Foundation; Japan Society for the Promotion of Science Grants-in-Aid for Scientific Research 17K19229 and 18H02136; and a JST Precursory Research for Embryonic Science and Technology Grant JPMJPR11B9 (to N.N.). Institute of Transformative Bio-Molecules is supported by the World Premier International Research Center Initiative, Japan.
Publisher Copyright:
© 2019 National Academy of Sciences. All rights reserved.
PY - 2019
Y1 - 2019
N2 - The circadian clock provides organisms with the ability to adapt to daily and seasonal cycles. Eukaryotic clocks mostly rely on lineage-specific transcriptional-translational feedback loops (TTFLs). Posttranslational modifications are also crucial for clock functions in fungi and animals, but the posttranslational modifications that affect the plant clock are less understood. Here, using chemical biology strategies, we show that the Arabidopsis CASEIN KINASE 1 LIKE (CKL) family is involved in posttranslational modification in the plant clock. Chemical screening demonstrated that an animal CDC7/CDK9 inhibitor, PHA767491, lengthens the Arabidopsis circadian period. Affinity proteomics using a chemical probe revealed that PHA767491 binds to and inhibits multiple CKL proteins, rather than CDC7/CDK9 homologs. Simultaneous knockdown of Arabidopsis CKL-encoding genes lengthened the circadian period. CKL4 phosphorylated transcriptional repressors PSEUDO-RESPONSE REGULATOR 5 (PRR5) and TIMING OF CAB EXPRESSION 1 (TOC1) in the TTFL. PHA767491 treatment resulted in accumulation of PRR5 and TOC1, accompanied by decreasing expression of PRR5- and TOC1-target genes. A prr5 toc1 double mutant was hyposensitive to PHA767491-induced period lengthening. Together, our results reveal posttranslational modification of transcriptional repressors in plant clock TTFL by CK1 family proteins, which also modulate nonplant circadian clocks.
AB - The circadian clock provides organisms with the ability to adapt to daily and seasonal cycles. Eukaryotic clocks mostly rely on lineage-specific transcriptional-translational feedback loops (TTFLs). Posttranslational modifications are also crucial for clock functions in fungi and animals, but the posttranslational modifications that affect the plant clock are less understood. Here, using chemical biology strategies, we show that the Arabidopsis CASEIN KINASE 1 LIKE (CKL) family is involved in posttranslational modification in the plant clock. Chemical screening demonstrated that an animal CDC7/CDK9 inhibitor, PHA767491, lengthens the Arabidopsis circadian period. Affinity proteomics using a chemical probe revealed that PHA767491 binds to and inhibits multiple CKL proteins, rather than CDC7/CDK9 homologs. Simultaneous knockdown of Arabidopsis CKL-encoding genes lengthened the circadian period. CKL4 phosphorylated transcriptional repressors PSEUDO-RESPONSE REGULATOR 5 (PRR5) and TIMING OF CAB EXPRESSION 1 (TOC1) in the TTFL. PHA767491 treatment resulted in accumulation of PRR5 and TOC1, accompanied by decreasing expression of PRR5- and TOC1-target genes. A prr5 toc1 double mutant was hyposensitive to PHA767491-induced period lengthening. Together, our results reveal posttranslational modification of transcriptional repressors in plant clock TTFL by CK1 family proteins, which also modulate nonplant circadian clocks.
KW - Arabidopsis
KW - Circadian clock
KW - Posttranslational regulation
KW - Small molecule
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UR - http://www.scopus.com/inward/citedby.url?scp=85066801325&partnerID=8YFLogxK
U2 - 10.1073/pnas.1903357116
DO - 10.1073/pnas.1903357116
M3 - Article
C2 - 31097584
AN - SCOPUS:85066801325
SN - 0027-8424
VL - 166
SP - 11528
EP - 11536
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 - 23
ER -