Golldack Dortje, Quigley Francoise, Michalowski Christine B, Kamasani Uma R, Bohnert Hans J
Department of Biochemistry, University of Arizona, Tucson, AZ 85721, USA.
Plant Mol Biol. 2003 Jan;51(1):71-81. doi: 10.1023/a:1020763218045.
In the indica rice (Oryza sativa L.) a cDNA was characterized that encoded OsAKT1 homologous to inward-rectifying potassium channels of the AKT/KAT subfamily. Transcript analysis located OsAKT1 predominantly in roots with low abundance in leaves. Cell-specificity of OsAKT expression was analyzed by in situ hybridizations. In roots, strongest signals were localized to the epidermis and the endodermis, whereas lower transcript levels were detected in cells of the vasculature and the cortex. In leaves, expression was detected in xylem parenchyma, phloem, and mesophyll cells. Transcriptional regulation and cell specificity of OsAKT1 during salt stress was compared in rice lines showing different salinity tolerance. In the salt-tolerant, sodium-excluding varieties Pokkali and BK, OsAKT1 transcripts disappeared from the exodermis in plants treated with 150 mM NaCl for 48 h but OsAKT1 transcription was not repressed in these cells in the salt-sensitive, sodium-accumulating variety IR29. Significantly, all lines were able to maintain potassium levels under sodium stress conditions, while sodium concentrations in the leaves of IR29 increased 5-10-fold relative to the sodium concentration in BK or Pokkali. The divergent, line-dependent and salt-dependent, regulation of this channel does not significantly affect potassium homeostasis under salinity stress. Rather, repression in Pokkali/BK and lack of repression in IR29 correlate with the overall tolerance character of these lines.
在籼稻(Oryza sativa L.)中,一个cDNA被鉴定出来,它编码与AKT/KAT亚家族内向整流钾通道同源的OsAKT1。转录本分析表明,OsAKT1主要位于根部,在叶片中的丰度较低。通过原位杂交分析了OsAKT表达的细胞特异性。在根部,最强的信号定位于表皮和内皮层,而在维管组织和皮层细胞中检测到较低的转录水平。在叶片中,在木质部薄壁细胞、韧皮部和叶肉细胞中检测到表达。在表现出不同耐盐性的水稻品系中比较了盐胁迫期间OsAKT1的转录调控和细胞特异性。在耐盐、排钠品种Pokkali和BK中,用150 mM NaCl处理48小时的植物中,外皮层的OsAKT1转录本消失,但在盐敏感、钠积累品种IR29的这些细胞中,OsAKT1转录未被抑制。值得注意的是,所有品系在钠胁迫条件下都能够维持钾水平,而IR29叶片中的钠浓度相对于BK或Pokkali中的钠浓度增加了5至10倍。该通道的不同的、依赖品系和依赖盐胁迫的调控在盐胁迫下对钾稳态没有显著影响。相反,Pokkali/BK中的抑制和IR29中缺乏抑制与这些品系的总体耐受性特征相关。