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Molecular Plant 2008 1(6):938-949; doi:10.1093/mp/ssn064
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© The Author 2008. Published by the Molecular Plant Shanghai Editorial Office in association with Oxford University Press on behalf of CSPP and IPPE, SIBS, CAS.

Targeting of Vacuolar Membrane Localized Members of the TPK Channel Family

Marcel Dunkela, Andreas Latza,c, Karin Schumacherb, Thomas Müllera, Dirk Beckera and Rainer Hedricha,1

a Molecular Plant Physiology and Biophysics, Julius-von-Sachs-Institute, University of Würzburg, Julius-von-Sachs-Platz 2, 97082 Würzburg, Germany
b Heidelberger Institut für Pflanzenwissenschaften (HIP), University of Heidelberg, Im Neuenheimer Feld 230, 69120 Heidelberg, Germany (K.S.)
c Present address: Physiological Ecology of Plants, University of Tübingen, Auf der Morgenstelle 1, 72076 Tübingen, Germany

1 To whom correspondence should be addressed at the Department of Molecular Plant Physiology and Biophysics. E-mail hedrich{at}botanik.uni-wuerzburg.de, fax +49 (0)931/888-6157, tel. +49 (0)931/888-6100.

Four members of the tandem-pore potassium channel family of Arabidopsis thaliana (TPK1, 2, 3, and 5) reside in the vacuolar membrane, whereas TPK4 is a plasma membrane K+-channel. By constructing chimeras between TPK1 and TPK4, we attempted to identify channel domains involved in the trafficking process and found that the TPK1 cytoplasmic C-terminal domain (CT) is critical for the ER- as well as Golgi-sorting steps. Following site-directed mutagenesis, we identified a diacidic motif (DLE) required for ER-export of TPK1. However, this diacidic motif in the C-terminus is not conserved among other members of the TPK family, and TPK3 sorting is independent of its CT. Moreover, the 14-3-3 binding site of TPK1, essential for channel activation, is not involved in channel sorting.


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