Assessment of sequence polymorphism and gene expression of OsSOS1 gene in two contrasting rice genotypes

P. T. Do, H. Pham, H. Nguyen, D. H. Le
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引用次数: 1

Abstract

Salt stress causes severe reduction in the growth and yield of rice plants. The ability to maintain cellular ion homeostasis is of importance to help the plant survive under salt stress. Salt overly sensitive 1 (SOS1), a plasma membrane Na+/H+ antiporter, has been proven to play critical roles in Na+ exclusion out of the cell, hence contributing to salt tolerance in plants. In this study, we analyzed the natural nucleotide polymorphisms occuring within the entire coding sequence as well as the upstream region of the OsSOS1 gene by comparing the sequences of two contrasting rice genotypes, namely, Nipponbare (salt-sensitive) and Pokkali (salt-resistant). In total, six nucleotide polymorphisms were identified in the coding sequence, and 44 nucleotide substitutions, 225-bp-insertion and 65-bp-deletion were observed in the upstream region of the OsSOS1 gene. Futher in silico analysis revealed that two out of six nucleotide polymorphisms in the coding sequence were non-synonymous (A1600G, G2204A) which led to two amino acid substitutions (T534A, S735N, respectively) positioned in the C-terminal domain of OsSOS1 transporter, but caused no effect on protein properties. In the upstream region of OsSOS1 gene, 44 single nucleotide polymorphisms and two INDELs were identified, in which nucleotide substitutions at position -1392, -1389, -822, -583, +57 and an insertion at position -1035 caused change in cis-regulatory elements. Analysis of OsSOS1 expression revealed that salt induced the expression of the gene in the roots, but not in the leaves in both investigated rice cultivars.
两种水稻OsSOS1基因型序列多态性及基因表达分析
盐胁迫严重影响水稻的生长和产量。维持细胞离子平衡的能力对于帮助植物在盐胁迫下生存至关重要。盐过度敏感1 (SOS1)是一种质膜Na+/H+反转运蛋白,已被证明在Na+排除细胞外的过程中起关键作用,从而有助于植物的耐盐性。本研究通过比较Nipponbare(盐敏感型)和Pokkali(耐盐型)两种水稻基因型的序列,分析了OsSOS1基因整个编码序列以及上游区域的天然核苷酸多态性。在编码序列中共鉴定出6个核苷酸多态性,在OsSOS1基因上游区域发现44个核苷酸替换,插入225 bp和缺失65 bp。进一步的硅分析显示,编码序列的6个核苷酸多态性中有2个是非同义的(A1600G, G2204A),导致位于OsSOS1转运体c端结构域的两个氨基酸替换(分别为T534A, S735N),但对蛋白质性质没有影响。在OsSOS1基因上游区域,鉴定出44个单核苷酸多态性和2个indel,其中-1392、-1389、-822、-583、+57位点的核苷酸替换和-1035位点的插入导致顺式调控元件的变化。对OsSOS1基因的表达分析表明,盐诱导该基因在根中表达,而在叶片中不表达。
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