USDA-ARS, Crop Germplasm Research, College Station, TX 77845, USA ; Texas A&M AgriLife Research and Extension Center, Dallas, TX 75252, USA.
Department of Plant Pathology, Texas A&M University, College Station, TX 77843, USA.
Int J Genomics. 2015;2015:528395. doi: 10.1155/2015/528395. Epub 2015 Jul 12.
Transcriptome analysis was conducted in two popular Lagerstroemia cultivars: "Natchez" (NAT), a white flower and powdery mildew resistant interspecific hybrid and "Carolina Beauty" (CAB), a red flower and powdery mildew susceptible L. indica cultivar. RNA-seq reads were generated from Erysiphe australiana infected leaves and de novo assembled. A total of 37,035 unigenes from 224,443 assembled contigs in both genotypes were identified. Approximately 85% of these unigenes have known function. Of them, 475 KEGG genes were found significantly different between the two genotypes. Five of the top ten differentially expressed genes (DEGs) involved in the biosynthesis of secondary metabolites (plant defense) and four in flavonoid biosynthesis pathway (antioxidant activities or flower coloration). Furthermore, 5 of the 12 assembled unigenes in benzoxazinoid biosynthesis and 7 of 11 in flavonoid biosynthesis showed higher transcript abundance in NAT. The relative abundance of transcripts for 16 candidate DEGs (9 from CAB and 7 from NAT) detected by qRT-PCR showed general agreement with the abundances of the assembled transcripts in NAT. This study provided the first transcriptome analyses in L. indica. The differential transcript abundance between two genotypes indicates that it is possible to identify candidate genes that are associated with the plant defenses or flower coloration.
“纳切兹”(NAT),一个白色的花和白粉病抗性种间杂种和“卡罗莱纳美”(CAB),一个红色的花和白粉病敏感的 L. indica 品种。从 Erysiphe australiana 感染的叶片中生成 RNA-seq 读取,并从头组装。总共从 22443 个组装的连续体中鉴定出 37035 个来自两个基因型的 unigenes。这些 unigenes中约有 85%具有已知功能。其中,在两个基因型之间发现 475 个 KEGG 基因存在显著差异。前十个差异表达基因(DEGs)中有五个参与次生代谢物(植物防御)的生物合成,四个在类黄酮生物合成途径(抗氧化活性或花色)。此外,在苯并恶嗪生物合成中组装的 12 个 unigenes中的 5 个和类黄酮生物合成中的 11 个中的 7 个在 NAT 中表现出更高的转录丰度。通过 qRT-PCR 检测的 16 个候选 DEGs(9 个来自 CAB,7 个来自 NAT)的转录本相对丰度与 NAT 中组装的转录本的丰度基本一致。这项研究提供了 L. indica 的首次转录组分析。两个基因型之间的差异转录丰度表明,可以鉴定与植物防御或花色相关的候选基因。