Informace o publikaci

Histidine kinase inhibitors impair shoot regeneration in Arabidopsis thaliana via cytokinin signaling and SAM patterning determinants

Autoři	LARDON Robin TRINH Hoang Khai XU Xiangyu VU Lam Dai VAN DE COTTE Brigitte PERNISOVÁ Markéta VANNESTE Steffen DE SMET Ive GEELEN Danny
Rok publikování	2022
Druh	Článek v odborném periodiku
Časopis / Zdroj	Frontiers in Plant Science
Fakulta / Pracoviště MU	Přírodovědecká fakulta
Citace
www	https://www.frontiersin.org/articles/10.3389/fpls.2022.894208/full
Doi	http://dx.doi.org/10.3389/fpls.2022.894208
Klíčová slova	phosphoproteomics; kinase inhibitors; cytokinin signaling; shoot regeneration; organogenesis
Popis	Reversible protein phosphorylation is a post-translational modification involved in virtually all plant processes, as it mediates protein activity and signal transduction. Here, we probe dynamic protein phosphorylation during de novo shoot organogenesis in Arabidopsis thaliana. We find that application of three kinase inhibitors in various time intervals has different effects on root explants. Short exposures to the putative histidine (His) kinase inhibitor TCSA during the initial days on shoot induction medium (SIM) are detrimental for regeneration in seven natural accessions. Investigation of cytokinin signaling mutants, as well as reporter lines for hormone responses and shoot markers, suggests that TCSA impedes cytokinin signal transduction via AHK3, AHK4, AHP3, and AHP5. A mass spectrometry-based phosphoproteome analysis further reveals profound deregulation of Ser/Thr/Tyr phosphoproteins regulating protein modification, transcription, vesicle trafficking, organ morphogenesis, and cation transport. Among TCSA-responsive factors are prior candidates with a role in shoot apical meristem patterning, such as AGO1, BAM1, PLL5, FIP37, TOP1ALPHA, and RBR1, as well as proteins involved in polar auxin transport (e.g., PIN1) and brassinosteroid signaling (e.g., BIN2). Putative novel regeneration determinants regulated by TCSA include RD2, AT1G52780, PVA11, and AVT1C, while NAIP2, OPS, ARR1, QKY, and aquaporins exhibit differential phospholevels on control SIM. LC–MS/MS data are available via ProteomeXchange with identifier PXD030754.