Rong Liping, Li Qianzhong, Li Shushun, Tang Ling, Wen Jing
Institute of Horticulture, Jiangsu Academy of Agricultural Sciences/Jiangsu Key Laboratory for Horticultural Crop Genetic Improvement, Nanjing, China.
Mol Genet Genomics. 2016 Apr;291(2):575-86. doi: 10.1007/s00438-015-1127-2. Epub 2015 Oct 16.
Maple (Acer palmatum) is an important species for landscape planting worldwide. Salt stress affects the normal growth of the Maple leaf directly, leading to loss of esthetic value. However, the limited availability of Maple genomic information has hindered research on the mechanisms underlying this tolerance. In this study, we performed comprehensive analyses of the salt tolerance in two genotypes of Maple using RNA-seq. Approximately 146.4 million paired-end reads, representing 181,769 unigenes, were obtained. The N50 length of the unigenes was 738 bp, and their total length over 102.66 Mb. 14,090 simple sequence repeats and over 500,000 single nucleotide polymorphisms were identified, which represent useful resources for marker development. Importantly, 181,769 genes were detected in at least one library, and 303 differentially expressed genes (DEGs) were identified between salt-sensitive and salt-tolerant genotypes. Among these DEGs, 125 were upregulated and 178 were downregulated genes. Two MYB-related proteins and one LEA protein were detected among the first 10 most downregulated genes. Moreover, a methyltransferase-related gene was detected among the first 10 most upregulated genes. The three most significantly enriched pathways were plant hormone signal transduction, arginine and proline metabolism, and photosynthesis. The transcriptome analysis provided a rich genetic resource for gene discovery related to salt tolerance in Maple, and in closely related species. The data will serve as an important public information platform to further our understanding of the molecular mechanisms involved in salt tolerance in Maple.
枫树(鸡爪槭)是全球景观种植的重要树种。盐胁迫直接影响枫叶的正常生长,导致美学价值丧失。然而,枫树基因组信息的有限可用性阻碍了对这种耐受性潜在机制的研究。在本研究中,我们使用RNA测序对两种基因型的枫树的耐盐性进行了综合分析。获得了约1.464亿对末端测序读段,代表181,769个单基因。单基因的N50长度为738 bp,总长度超过1.0266 Mb。鉴定出14,090个简单序列重复和超过50万个单核苷酸多态性,它们是标记开发的有用资源。重要的是,在至少一个文库中检测到181,769个基因,并且在盐敏感和耐盐基因型之间鉴定出303个差异表达基因(DEG)。在这些DEG中,125个是上调基因,178个是下调基因。在前10个下调最显著的基因中检测到两种MYB相关蛋白和一种LEA蛋白。此外,在前10个上调最显著的基因中检测到一个与甲基转移酶相关的基因。三个最显著富集的途径是植物激素信号转导、精氨酸和脯氨酸代谢以及光合作用。转录组分析为与枫树以及密切相关物种的耐盐性相关的基因发现提供了丰富的遗传资源。这些数据将作为一个重要的公共信息平台,以加深我们对枫树耐盐性分子机制的理解。