HvALMT1 from barley is involved in the transport of organic anions

被引:86
作者
Gruber, Benjamin D. [1 ,3 ]
Ryan, Peter R. [1 ]
Richardson, Alan E. [1 ]
Tyerman, Stephen D. [2 ]
Ramesh, Sunita [2 ]
Hebb, Diane M. [1 ]
Howitt, Susan M. [3 ]
Delhaize, Emmanuel [1 ]
机构
[1] CSIRO Plant Ind, Canberra, ACT 2601, Australia
[2] Univ Adelaide, Sch Agr Food & Wine, Glen Osmond, SA 5064, Australia
[3] Australian Natl Univ, Sch Biochem & Mol Biol, Canberra, ACT 0200, Australia
关键词
Channel; HvALMT1; malate; oocytes; organic anion; stomata; CONTROLLING ALUMINUM TOLERANCE; PLASMA-MEMBRANE; GUARD-CELLS; MALATE TRANSPORTER; K+-CHANNEL; MALIC-ACID; ALT4; LOCUS; ALMT1; GENE; ARABIDOPSIS; IDENTIFICATION;
D O I
10.1093/jxb/erq023
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Members of the ALMT gene family contribute to the Al3+ resistance of several plant species by facilitating malate efflux from root cells. The first member of this family to be cloned and characterized, TaALMT1, is responsible for most of the natural variation of Al3+ resistance in wheat. The current study describes the isolation and characterization of HvALMT1, the barley gene with the greatest sequence similarity to TaALMT1. HvALMT1 is located on chromosome 2H which has not been associated with Al3+ resistance in barley. The relatively low levels of HvALMT1 expression detected in root and shoot tissues were independent of external aluminium or phosphorus supply. Transgenic barley plants transformed with the HvALMT1 promoter fused to the green fluorescent protein (GFP) indicated that expression of HvALMT1 was relatively high in stomatal guard cells and in root tissues containing expanding cells. GFP fused to the C-terminus of the full HvALMT1 protein localized to the plasma membrane and motile vesicles within the cytoplasm. HvALMT1 conferred both inward and outward currents when expressed in Xenopus laevis oocytes that were bathed in a range of anions including malate. Both malate uptake and efflux were confirmed in oocyte assays using [C-14]malate as a radiotracer. It is suggested that HvALMT1 functions as an anion channel to facilitate organic anion transport in stomatal function and expanding cells.
引用
收藏
页码:1455 / 1467
页数:13
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