Graduate Program of Plant Biotechnology, Federal University of Lavras, 37200-000, Lavras, MG, CP 3037, Brazil.
Brazilian Agricultural Research Corporation, Embrapa Agroenergy, 70770-901, Brasília, DF, Brazil.
BMC Genomics. 2022 Oct 31;23(1):735. doi: 10.1186/s12864-022-08926-6.
Soil salinity is a problem in more than 100 countries across all continents. It is one of the abiotic stress that threatens agriculture the most, negatively affecting crops and reducing productivity. Transcriptomics is a technology applied to characterize the transcriptome in a cell, tissue, or organism at a given time via RNA-Seq, also known as full-transcriptome shotgun sequencing. This technology allows the identification of most genes expressed at a particular stage, and different isoforms are separated and transcript expression levels measured. Once determined by this technology, the expression profile of a gene must undergo validation by another, such as quantitative real-time PCR (qRT-PCR). This study aimed to select, annotate, and validate stress-inducible genes-and their promoters-differentially expressed in the leaves of oil palm (Elaeis guineensis) plants under saline stress.
The transcriptome analysis led to the selection of 14 genes that underwent structural and functional annotation, besides having their expression validated using the qRT-PCR technique. When compared, the RNA-Seq and qRT-PCR profiles of those genes resulted in some inconsistencies. The structural and functional annotation analysis of proteins coded by the selected genes showed that some of them are orthologs of genes reported as conferring resistance to salinity in other species. There were those coding for proteins related to the transport of salt into and out of cells, transcriptional regulatory activity, and opening and closing of stomata. The annotation analysis performed on the promoter sequence revealed 22 distinct types of cis-acting elements, and 14 of them are known to be involved in abiotic stress.
This study has helped validate the process of an accurate selection of genes responsive to salt stress with a specific and predefined expression profile and their promoter sequence. Its results also can be used in molecular-genetics-assisted breeding programs. In addition, using the identified genes is a window of opportunity for strategies trying to relieve the damages arising from the salt stress in many glycophyte crops with economic importance.
土壤盐渍化是一个在各大洲超过 100 个国家都存在的问题。它是威胁农业的最主要非生物胁迫因素之一,对作物产生负面影响,降低生产力。转录组学是一种通过 RNA-Seq(也称为全转录组鸟枪法测序)在特定时间对细胞、组织或生物体的转录组进行特征描述的技术。该技术可以识别特定阶段表达的大多数基因,并分离不同的异构体,测量转录表达水平。通过该技术确定后,必须通过另一种技术(如定量实时 PCR(qRT-PCR))验证基因的表达谱。本研究旨在选择、注释和验证在盐胁迫下油棕(Elaeis guineensis)叶片中差异表达的诱导应激基因及其启动子。
转录组分析导致选择了 14 个基因,这些基因进行了结构和功能注释,并且使用 qRT-PCR 技术验证了它们的表达。比较时,这些基因的 RNA-Seq 和 qRT-PCR 图谱存在一些不一致。所选基因编码蛋白的结构和功能注释分析表明,其中一些是其他物种中报道的耐盐性基因的同源物。有一些编码与盐进出细胞运输、转录调控活性和气孔开闭有关的蛋白。对启动子序列的注释分析揭示了 22 种不同类型的顺式作用元件,其中 14 种已知参与非生物胁迫。
本研究有助于验证准确选择具有特定和预定义表达谱的盐胁迫响应基因及其启动子序列的过程。其结果还可用于分子遗传学辅助育种计划。此外,利用鉴定出的基因是一种机会之窗,可以尝试减轻许多具有经济重要性的糖质作物因盐胁迫而产生的损害的策略。