Park Jong-Won, Benatti Thiago R, Marconi Thiago, Yu Qingyi, Solis-Gracia Nora, Mora Victoria, da Silva Jorge A
Texas A&M AgriLife Research, The Texas A&M System, Weslaco, Texas, United States of America.
Texas A&M AgriLife Research, The Texas A&M System, Dallas, Texas, United States of America.
PLoS One. 2015 May 4;10(5):e0125810. doi: 10.1371/journal.pone.0125810. eCollection 2015.
Transcriptome analysis of sugarcane hybrid CP72-1210 (cold susceptible) and Saccharum spontaneum TUS05-05 (cold tolerant) using Sugarcane Assembled Sequences (SAS) from SUCEST-FUN Database showed that a total of 35,340 and 34,698 SAS genes, respectively, were expressed before and after chilling stress. The analysis revealed that more than 600 genes are differentially expressed in each genotype after chilling stress. Blast2Go annotation revealed that the major difference in gene expression profiles between CP72-1210 and TUS05-05 after chilling stress are present in the genes related to the transmembrane transporter activity. To further investigate the relevance of transmembrane transporter activity against abiotic stress tolerance, a S. spontaneum homolog of a NOD26-like major intrinsic protein gene (SspNIP2) was selected for functional analysis, of which expression was induced after chilling stress in the cold tolerant TUS05-05. Quantitative real-time PCR showed that SspNIP2 expression was increased ~2.5 fold at 30 minutes after cold treatment and stayed induced throughout the 24 hours of cold treatment. The amino acid sequence analysis of the cloned SspNIP2 confirmed the presence of six transmembrane domains and two NPA (Asn-Pro-Ala) motifs, signature features of major intrinsic protein families. Amino acid analysis confirmed that four amino acids, comprising the ar/R (aromatic residue/arginine) region responsible for the substrate specificity among MIPs, are conserved among monocot silicon transporters and SspNIP2. Salinity stress test on SspNIP2 transgenic tobacco plants resulted in more vigorous transgenic lines than the non-transgenic tobacco plants, suggesting some degree of tolerance to salt stress conferred by SspNIP2. SspNIP2-transgenic plants, exposed to 2 weeks of water stress without irrigation, developed various degrees of water stress symptom. The water stress test confirmed that the SspNIP2 transgenic lines had lower evapotranspiration rates than non-transgenic lines, suggesting that SspNIP2 transgenic lines showed a slight tolerance to the early water stress compared to wild type plants.
利用来自SUCEST - FUN数据库的甘蔗组装序列(SAS)对甘蔗杂交种CP72 - 1210(冷敏感型)和甜根子草TUS05 - 05(耐冷型)进行转录组分析,结果表明,在冷胁迫前后分别共有35340个和34698个SAS基因表达。分析显示,每种基因型在冷胁迫后有600多个基因差异表达。Blast2Go注释显示,冷胁迫后CP72 - 1210和TUS05 - 05基因表达谱的主要差异存在于与跨膜转运蛋白活性相关的基因中。为了进一步研究跨膜转运蛋白活性与非生物胁迫耐受性的相关性(耐冷型TUS05 - 05在冷胁迫后诱导表达),选择了一个类NOD26主要内在蛋白基因(SspNIP2)的甜根子草同源物进行功能分析。定量实时PCR显示,冷处理30分钟后SspNIP2表达增加约2.5倍,并在整个24小时冷处理过程中持续诱导表达。对克隆的SspNIP2进行氨基酸序列分析,证实其存在6个跨膜结构域和2个NPA(天冬酰胺 - 脯氨酸 - 丙氨酸)基序,这是主要内在蛋白家族的特征性结构。氨基酸分析证实,在单子叶植物硅转运蛋白和SspNIP2中,负责MIPs底物特异性的由4个氨基酸组成的ar/R(芳香族残基/精氨酸)区域是保守的。对SspNIP2转基因烟草植株进行盐胁迫试验,结果显示转基因株系比非转基因烟草植株生长更旺盛,这表明SspNIP2赋予了一定程度的耐盐胁迫能力。对SspNIP2转基因植株进行2周无灌溉水分胁迫试验,植株出现了不同程度的水分胁迫症状。水分胁迫试验证实,SspNIP2转基因株系的蒸散速率低于非转基因株系,这表明与野生型植株相比,SspNIP2转基因株系对早期水分胁迫表现出轻微的耐受性。