Light Controls Cytokinin Signaling via Transcriptional Regulation of Constitutively Active Sensor Histidine Kinase CKI1

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Publikace nespadá pod Ústav výpočetní techniky, ale pod Středoevropský technologický institut. Oficiální stránka publikace je na webu muni.cz.
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DOBISOVÁ Tereza HRDINOVÁ Vendula CUESTA Candela MICHLÍČKOVÁ Šárka URBÁNKOVÁ Ivana HEJÁTKOVÁ Romana ŽÁDNÍKOVÁ Petra PERNISOVÁ Markéta BENKOVÁ Eva HEJÁTKO Jan

Rok publikování 2017
Druh Článek v odborném periodiku
Časopis / Zdroj Plant Physiology
Fakulta / Pracoviště MU

Středoevropský technologický institut

Citace
www https://academic.oup.com/plphys/article/174/1/387/6116747
Doi http://dx.doi.org/10.1104/pp.16.01964
Obor Genetika a molekulární biologie
Klíčová slova light; cytokinin; signalling; CKI1
Popis In plants, the multistep phosphorelay (MSP) pathway mediates a range of regulatory processes, including those activated by cytokinins. The crosstalk between cytokinin response and light is known for a long time. However, the molecular mechanism underlying the interaction between light and cytokinin signaling remains elusive. In the screen for upstream regulators we identified a LONG PALE HYPOCOTYL (LPH) gene whose activity is indispensable for spatiotemporally correct expression of CYTOKININ INDEPENDENT-1 (CKI1), encoding the constitutively active sensor histidine kinase that activates MSP signaling. lph is a new allele of HEME OXYGENASE 1 (HY1) which encodes the key protein in the biosynthesis of phytochromobilin, a cofactor of photoconvertible phytochromes. Our analysis confirmed the light-dependent regulation of the CKI1 expression pattern. We show that CKI1 expression is under the control of phytochrome A (phyA), functioning as a dual (both positive and negative) regulator of CKI1 expression, presumably via the phyA-regulated transcription factors PHYTOCHROME INTERACTING FACTOR 3 (PIF3) and CIRCADIAN CLOCK ASSOCIATED 1 (CCA1). Changes in CKI1 expression observed in lph/hy1-7 and phy mutants correlate with misregulation of MSP signaling, changed cytokinin sensitivity and developmental aberrations, previously shown to be associated with cytokinin and/or CKI1 action. Besides that, we demonstrate novel role of phyA-dependent CKI1 expression in the hypocotyl elongation and hook development during skotomorphogenesis. Based on these results, we propose that the light-dependent regulation of CKI1 provides a plausible mechanistic link underlying the well-known interaction between light- and cytokinin controlled plant development.
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