Abstract

In search of K(+) channel genes expressed in the leaf of the C(4) plant Zea mays, we isolated the cDNA of KZM1 (for K(+) channel Zea mays 1). KZM1 showed highest similarity to the Arabidopsis K(+) channels KAT1 and KAT2, which are localized in guard cells and phloem. When expressed in Xenopus oocytes, KZM1 exhibited the characteristic features of an inward-rectifying, potassium-selective channel. In contrast to KAT1- and KAT2-type K(+) channels, however, KZM1 currents were insensitive to external pH changes. Northern blot analyses identified the leaf, nodes, and silks as sites of KZM1 expression. Following the separation of maize leaves into epidermal, mesophyll, and vascular fractions, quantitative real-time reverse transcriptase-PCR allowed us to localize KZM1 transcripts predominantly in vascular strands and the epidermis. Cell tissue separation and KZM1 localization were followed with marker genes such as the bundle sheath-specific ribulose-1,5-bisphosphate carboxylase, the phloem K(+) channel ZMK2, and the putative sucrose transporter ZmSUT1. When expressed in Xenopus oocytes, ZmSUT1 mediated proton-coupled sucrose symport. Coexpression of ZmSUT1 with the phloem K(+) channels KZM1 and ZMK2 revealed that ZMK2 is able to stabilize the membrane potential during phloem loading/unloading processes and KZM1 to mediate K(+) uptake. During leaf development, sink-source transitions, and diurnal changes, KZM1 is constitutively expressed, pointing to a housekeeping function of this channel in K(+) homeostasis of the maize leaf. Therefore, the voltage-dependent K(+)-uptake channel KZM1 seems to mediate K(+) retrieval and K(+) loading into the phloem as well as K(+)-dependent stomatal opening.

Highlights

  • Since the first isolation of a plant Kϩ channel gene 10 years ago, plant science has focused on their cell-specific localization and structure-function relationship

  • By heterologous expression in Xenopus oocytes, we showed that ZmSUT1 represents a sucrose/Hϩ symporter under the voltage control of the AKT2/3 ortholog ZMK2

  • In contrast to ZMK2, the sequence of KZM1 did not contain an ankyrin binding domain (Fig. 1A), a feature that is conserved among Kϩ channels of the KAT1 subfamily [1], beside the SIRK protein from Vitis vinifera [22] and KPT1 from Populus tremula (GenBankTM accession number AJ344623, for details see “Discussion”)

Read more

Summary

Introduction

Since the first isolation of a plant Kϩ channel gene 10 years ago, plant science has focused on their cell-specific localization and structure-function relationship. Family of Arabidopsis Kϩ channels consists of nine members (for review see Ref. 2) According to their localization, structure, and function, these genes can be assigned to different subfamilies. In contrast to the mentioned inward rectifiers within the AKT1 and KAT1 family, members of the AKT2/3 subfamily are characterized by weak voltage dependence, a Ca2ϩ and Hϩ block, and seem to control phloem function (16 –19). The maize plant is a model system for monocotyledonous crops but C4 photosynthesis as well This involves a special anatomic feature called Kranz anatomy: mesophyll cells, involved in the prefixation of CO2, transport C4 compounds to the bundle sheath cells, which surround the vascular strands and fix CO2 in the Calvin cycle (reviewed in Ref. 25). By heterologous expression in Xenopus oocytes, we showed that ZmSUT1 represents a sucrose/Hϩ symporter under the voltage control of the AKT2/3 ortholog ZMK2

Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call