Phosphorylation-Mediated Dynamics of Nitrate Transceptor NRT1.1 Regulate Auxin Flux and Nitrate Signaling in Lateral Root Growth1[OPEN]
The differential phosphorylation of nitrate transceptor NRT1.1 contributes to the modulation of lateral root development through spatiotemporal plasma membrane dynamics and cellular trafficking. The dual-affinity nitrate transceptor NITRATE TRANSPORTER1.1 (NRT1.1) has two modes of transport and sign...
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Veröffentlicht in: | Plant physiology (Bethesda) 2019-08, Vol.181 (2), p.480-498 |
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Hauptverfasser: | , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | The differential phosphorylation of nitrate transceptor NRT1.1 contributes to the modulation of lateral root development through spatiotemporal plasma membrane dynamics and cellular trafficking.
The dual-affinity nitrate transceptor NITRATE TRANSPORTER1.1 (NRT1.1) has two modes of transport and signaling, governed by Thr-101 (T101) phosphorylation. NRT1.1 regulates lateral root (LR) development by modulating nitrate-dependent basipetal auxin export and nitrate-mediated signal transduction. Here, using the Arabidopsis (
Arabidopsis thaliana
) NRT1.1
T101D
phosphomimetic and NRT1.1
T101A
nonphosphorylatable mutants, we found that the phosphorylation state of NRT1.1 plays a key role in NRT1.1 function during LR development. Single-particle tracking revealed that phosphorylation affected NRT1.1 spatiotemporal dynamics. The phosphomimetic NRT1.1
T101D
form showed fast lateral mobility and membrane partitioning that facilitated auxin flux under low-nitrate conditions. By contrast, nonphosphorylatable NRT1.1
T101A
showed low lateral mobility and oligomerized at the plasma membrane (PM), where it induced endocytosis via the clathrin-mediated endocytosis and microdomain-mediated endocytosis pathways under high-nitrate conditions. These behaviors promoted LR development by suppressing NRT1.1-controlled auxin transport on the PM and stimulating Ca
2+
-ARABIDOPSIS NITRATE REGULATED1 signaling from the endosome. |
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ISSN: | 0032-0889 1532-2548 |
DOI: | 10.1104/pp.19.00346 |