Root development under metal stress in Arabidopsis thaliana requires the H+/cation antiporter CAX4

* The Arabidopsis vacuolar CAtion eXchangers (CAXs) play a key role in mediating cation influx into the vacuole. In Arabidopsis, there are six CAX genes. However, some members are yet to be characterized fully. * In this study, we show that CAX4 is expressed in the root apex and lateral root primord...

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Détails bibliographiques
Publié dans:The New phytologist. - 1979. - 183(2009), 1 vom: 12., Seite 95-105
Auteur principal: Mei, Hui (Auteur)
Autres auteurs: Cheng, Ning Hui, Zhao, Jian, Park, Sunghun, Escareno, Rito A, Pittman, Jon K, Hirschi, Kendal D
Format: Article en ligne
Langue:English
Publié: 2009
Accès à la collection:The New phytologist
Sujets:Journal Article Research Support, U.S. Gov't, Non-P.H.S. Antiporters Arabidopsis Proteins CAX4 protein, Arabidopsis Cation Transport Proteins Indoleacetic Acids Metals, Heavy
Description
Résumé:* The Arabidopsis vacuolar CAtion eXchangers (CAXs) play a key role in mediating cation influx into the vacuole. In Arabidopsis, there are six CAX genes. However, some members are yet to be characterized fully. * In this study, we show that CAX4 is expressed in the root apex and lateral root primordia, and that expression is increased when Ni(2+) or Mn(2+) levels are elevated or Ca(2+) is depleted. * Transgenic plants expressing increased levels of CAX4 display symptoms consistent with increased sequestration of Ca(2+) and Cd(2+) into the vacuole. When CAX4 is highly expressed in an Arabidopsis cax1 mutant line with weak vacuolar Ca(2+)/H(+) antiport activity, a 29% increase in Ca(2+)/H(+) antiport is measured. A cax4 loss-of-function mutant and CAX4 RNA interference lines display altered root growth in response to Cd(2+), Mn(2+) and auxin. The DR5::GUS auxin reporter detected reduces auxin responses in the cax4 lines. * These results indicate that CAX4 is a cation/H(+) antiporter that plays an important function in root growth under heavy metal stress conditions
Description:Date Completed 30.11.2009
Date Revised 08.04.2022
published: Print-Electronic
Citation Status MEDLINE
ISSN:1469-8137
DOI:10.1111/j.1469-8137.2009.02831.x