| Literature DB >> 35085386 |
Ren Wang1,2, Ellie Himschoot1,2, Matteo Grenzi3, Jian Chen1,2, Alaeddine Safi1,2, Melanie Krebs4, Karin Schumacher4, Moritz K Nowack1,2, Wolfgang Moeder5, Keiko Yoshioka5, Daniël Van Damme1,2, Ive De Smet1,2, Danny Geelen6, Tom Beeckman1,2, Jiří Friml7, Alex Costa3,8, Steffen Vanneste1,6,9.
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.Entities:
Keywords: Arabidopsis; PIN protein; auxin analogs; calcium; endosomes; root; signaling; trafficking
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Year: 2022 PMID: 35085386 PMCID: PMC7612644 DOI: 10.1093/jxb/erac019
Source DB: PubMed Journal: J Exp Bot ISSN: 0022-0957 Impact factor: 7.298