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Na+ ,K /H+ antiporters regulate the pH of endoplasmic reticulum and auxin-mediated development
L. Fan, L. Zhao, W. Hu, W. Li, O. Novák, M. Strnad, S. Simon, J. Friml, J. Shen, L. Jiang, QS. Qiu,
Language English Country United States
Document type Journal Article, Research Support, Non-U.S. Gov't
NLK
Free Medical Journals
from 1997 to 3 years ago
Wiley Free Content
from 1997 to 3 years ago
PubMed
29360148
DOI
10.1111/pce.13153
Knihovny.cz E-resources
- MeSH
- Arabidopsis genetics growth & development metabolism MeSH
- Endoplasmic Reticulum metabolism MeSH
- Homeostasis MeSH
- Immunoprecipitation MeSH
- Hydrogen-Ion Concentration MeSH
- Indoleacetic Acids metabolism MeSH
- Membrane Transport Proteins metabolism MeSH
- Sodium-Hydrogen Exchangers metabolism MeSH
- Promoter Regions, Genetic genetics MeSH
- Arabidopsis Proteins metabolism MeSH
- Genes, Plant MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
AtNHX5 and AtNHX6 are endosomal Na+ ,K+ /H+ antiporters that are critical for growth and development in Arabidopsis, but the mechanism behind their action remains unknown. Here, we report that AtNHX5 and AtNHX6, functioning as H+ leak, control auxin homeostasis and auxin-mediated development. We found that nhx5 nhx6 exhibited growth variations of auxin-related defects. We further showed that nhx5 nhx6 was affected in auxin homeostasis. Genetic analysis showed that AtNHX5 and AtNHX6 were required for the function of the endoplasmic reticulum (ER)-localized auxin transporter PIN5. Although AtNHX5 and AtNHX6 were colocalized with PIN5 at ER, they did not interact directly. Instead, the conserved acidic residues in AtNHX5 and AtNHX6, which are essential for exchange activity, were required for PIN5 function. AtNHX5 and AtNHX6 regulated the pH in ER. Overall, AtNHX5 and AtNHX6 may regulate auxin transport across the ER via the pH gradient created by their transport activity. H+ -leak pathway provides a fine-tuning mechanism that controls cellular auxin fluxes.
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