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Published on October 28, 2005; 10.1104/pp.105.067553


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Received June 22, 2005
Returned for revision July 13, 2005
Accepted July 13, 2005

HKT1 Mediates Sodium Uniport in Roots. Pitfalls in the Expression of HKT1 in Yeast

Rosario Haro , María A. Bañuelos , María E. Senn , Javier Barrero-Gil , and Alonso Rodríguez-Navarro *

Departamento de Biotecnología, Universidad Politécnica de Madrid, 28040 Madrid, Spain

* Corresponding author; email: alonso.rodriguez{at}upm.es.

The function of HKT1 in roots is controversial. We tackled this controversy by studying Na+ uptake in barley (Hordeum vulgare) roots, cloning the HvHKT1 gene, and expressing the HvHKT1 cDNA in yeast (Saccharomyces cerevisiae) cells. High-affinity Na+ uptake was not detected in plants growing at high K+ but appeared soon after exposing the plants to a K+-free medium. It was a uniport, insensitive to external K+ at the beginning of K+ starvation and inhibitable by K+ several hours later. The expression of HvHKT1 in yeast was Na+ (or K+) uniport, Na+-K+ symport, or a mix of both, depending on the construct from which the transporter was expressed. The Na+ uniport function was insensitive to external K+ and mimicked the Na+ uptake carried out by the roots at the beginning of K+ starvation. The K+ uniport function only took place in yeast cells that were completely K+ starved and disappeared when internal K+ increased, which makes it unlikely that HvHKT1 mediates K+ uptake in roots. Mutation of the first in-frame AUG codon of HvHKT1 to CUC changed the uniport function into symport. The expression of the symport from either mutants or constructs keeping the first in-frame AUG took place only in K+-starved cells, while the uniport was expressed in all conditions. We discuss here that the symport occurs only in heterologous expression. It is most likely related to the K+ inhibitable Na+ uptake process of roots that heterologous systems fail to reproduce.




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