Australian Centre for Plant Functional Genomics, University of Adelaide, School of Agriculture Food and Wine, Hartley Grove, Urrbrae, PMB 1 Glen Osmond, SA 5064, Australia.
J Exp Bot. 2011 Jan;62(3):1201-16. doi: 10.1093/jxb/erq346. Epub 2010 Nov 3.
Genes that enable crops to limit Na(+) accumulation in shoot tissues represent potential sources of salinity tolerance for breeding. In barley, the HvNax4 locus lowered shoot Na(+) content by between 12% and 59% (g(-1) DW), or not at all, depending on the growth conditions in hydroponics and a range of soil types, indicating a strong influence of environment on expression. HvNax4 was fine-mapped on the long arm of barley chromosome 1H. Corresponding intervals of ∼200 kb, containing a total of 34 predicted genes, were defined in the sequenced rice and Brachypodium genomes. HvCBL4, a close barley homologue of the SOS3 salinity tolerance gene of Arabidopsis, co-segregated with HvNax4. No difference in HvCBL4 mRNA expression was detected between the mapping parents. However, genomic and cDNA sequences of the HvCBL4 alleles were obtained, revealing a single Ala111Thr amino acid substitution difference in the encoded proteins. The known crystal structure of SOS3 was used as a template to obtain molecular models of the barley proteins, resulting in structures very similar to that of SOS3. The position in SOS3 corresponding to the barley substitution does not participate directly in Ca(2+) binding, post-translational modifications or interaction with the SOS2 signalling partner. However, Thr111 but not Ala111 forms a predicted hydrogen bond with a neighbouring α-helix, which has potential implications for the overall structure and function of the barley protein. HvCBL4 therefore represents a candidate for HvNax4 that warrants further investigation.
能够使作物在茎组织中限制 Na(+)积累的基因代表了用于培育的耐盐性的潜在来源。在大麦中,HvNax4 基因座使茎中的 Na(+)含量降低了 12%至 59%(g(-1) DW),或者根本没有降低,这取决于水培和一系列土壤类型中的生长条件,这表明环境对表达有很强的影响。HvNax4 在大麦 1H 染色体的长臂上进行了精细定位。在测序的水稻和短柄草基因组中,相应的约 200 kb 区间,包含总共 34 个预测基因,被定义为。HvCBL4 是拟南芥 SOS3 耐盐基因的大麦近缘物,与 HvNax4 共分离。在作图亲本之间没有检测到 HvCBL4 mRNA 表达的差异。然而,获得了 HvCBL4 等位基因的基因组和 cDNA 序列,揭示了编码蛋白中单个 Ala111Thr 氨基酸取代差异。利用已知的 SOS3 晶体结构作为模板,获得了大麦蛋白的分子模型,得到的结构与 SOS3 的结构非常相似。SOS3 中对应于大麦取代的位置不直接参与 Ca(2+)结合、翻译后修饰或与 SOS2 信号伙伴的相互作用。然而,只有 Thr111 而不是 Ala111 与相邻的 α-螺旋形成预测的氢键,这对大麦蛋白的整体结构和功能有潜在影响。因此,HvCBL4 代表了 HvNax4 的候选基因,值得进一步研究。