Auxin analog-induced Ca2+ signaling is independent of inhibition of endosomal aggregation in Arabidopsis roots

Author:

Wang Ren12,Himschoot Ellie12ORCID,Grenzi Matteo3ORCID,Chen Jian12,Safi Alaeddine12ORCID,Krebs Melanie4ORCID,Schumacher Karin4ORCID,Nowack Moritz K12ORCID,Moeder Wolfgang5ORCID,Yoshioka Keiko5ORCID,Van Damme Daniël12ORCID,De Smet Ive12ORCID,Geelen Danny6ORCID,Beeckman Tom12ORCID,Friml Jiří7ORCID,Costa Alex38ORCID,Vanneste Steffen169ORCID

Affiliation:

1. Department of Plant Biotechnology and Bioinformatics, Ghent University, 9052 Ghent, Belgium

2. VIB Center for Plant Systems Biology, 9052 Ghent, Belgium

3. Department of Biosciences, University of Milan, 20133 Milan, Italy

4. Centre for Organismal Studies, Plant Developmental Biology, University of Heidelberg, 69120 Heidelberg, Germany

5. Department of Cell and Systems Biology, University of Toronto, Toronto, ON M5S 3B2, Canada

6. Department of Plants and Crops, Ghent University, 9000 Ghent, Belgium

7. Institute of Science and Technology Austria (IST Austria), 3400 Klosterneuburg, Austria

8. Institute of Biophysics, National Research Council of Italy (CNR), 20133 Milan, Italy

9. Lab of Plant Growth Analysis, Ghent University Global Campus, Incheon 21985, Republic of Korea

Abstract

Abstract Much of what we know about the role of auxin in plant development derives from exogenous manipulations of auxin distribution and signaling, using inhibitors, auxins, and auxin analogs. In this context, synthetic auxin analogs, such as 1-naphthalene acetic acid (1-NAA), are often favored over the endogenous auxin, indole-3-acetic acid (IAA), in part due to their higher stability. While such auxin analogs have proven instrumental in revealing the various faces of auxin, they display in some cases bioactivities distinct from IAA. Here, we focused on the effect of auxin analogs on the accumulation of PIN proteins in brefeldin A-sensitive endosomal aggregations (BFA bodies), and correlation with the ability to elicit Ca2+ responses. For a set of commonly used auxin analogs, we evaluated if auxin analog-induced Ca2+ signaling inhibits PIN accumulation. Not all auxin analogs elicited a Ca2+ response, and their differential ability to elicit Ca2+ responses correlated partially with their ability to inhibit BFA-body formation. However, in tir1/afb and cngc14, 1-NAA-induced Ca2+ signaling was strongly impaired, yet 1-NAA still could inhibit PIN accumulation in BFA bodies. This demonstrates that TIR1/AFB–CNGC14-dependent Ca2+ signaling does not inhibit BFA body formation in Arabidopsis roots.

Funder

China Scholarship Council

Fonds Wetenschappelijk Onderzoek

Ghent University

Deutsche Forschungsgemeinschaft

Piano di Sviluppo di Ateneo 2019

University of Milan

European Research Council T-Rex

Publisher

Oxford University Press (OUP)

Subject

Plant Science,Physiology

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