PIN3-mediated auxin transport contributes to blue light-induced adventitious root formation in Arabidopsis

•Blue light induces adventitious root formation through the blue light receptors, PHOT1 and PHOT2.•The phototropic transducer NPH3 functions in blue light-induced adventitious root formation.•NPH3 physically interacts with PIN3.•NPH3 regulates adventitious root formation by affecting PIN3-mediated a...

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Veröffentlicht in:Plant science (Limerick) 2021-11, Vol.312, p.111044-111044, Article 111044
Hauptverfasser: Zhai, Shuang, Cai, Wei, Xiang, Zhi-Xin, Chen, Cai-Yan, Lu, Ying-Tang, Yuan, Ting-Ting
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Sprache:eng
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Zusammenfassung:•Blue light induces adventitious root formation through the blue light receptors, PHOT1 and PHOT2.•The phototropic transducer NPH3 functions in blue light-induced adventitious root formation.•NPH3 physically interacts with PIN3.•NPH3 regulates adventitious root formation by affecting PIN3-mediated auxin transport. Adventitious rooting is a heritable quantitative trait that is influenced by multiple endogenous and exogenous factors in plants, and one important environmental factor required for efficient adventitious root formation is light signaling. However, the physiological significance and molecular mechanism of light underlying adventitious root formation are still largely unexplored. Here, we report that blue light-induced adventitious root formation is regulated by PIN-FORMED3 (PIN3)-mediated auxin transport in Arabidopsis. Adventitious root formation is significantly impaired in the loss-of-function mutants of the blue light receptors, PHOTOROPIN1 (PHOT1) and PHOTOROPIN2 (PHOT2), as well as the phototropic transducer, NON-PHOTOTROPIC HYPOCOTYL3 (NPH3). In addition, blue light enhanced the auxin content in the adventitious root, and the pin3 loss-of-function mutant had a reduced adventitious rooting response under blue light compared to the wild type. The PIN3 protein level was higher in plants treated with blue light than in those in darkness, especially in the hypocotyl pericycle, while PIN3-GFP failed to accumulate in nph3 PIN3::PIN3-GFP. Furthermore, the results showed that PIN3 physically interacted with NPH3, a key transducer in phototropic signaling. Taken together, our study demonstrates that blue light induces adventitious root formation through the phototropic signal transducer, NPH3, which regulates adventitious root formation by affecting PIN3-mediated auxin transport.
ISSN:0168-9452
1873-2259
DOI:10.1016/j.plantsci.2021.111044