Identification and validation of reference genes for real-time quantitative RT-PCR analysis in jute

• Published in: BMC molecular biology Vol. 20; no. 1; p. 13
• Main Authors: Hossain, Md Sabbir, Ahmed, Rasel, Haque, Md Samiul, Alam, Md Monjurul, Islam, Md Shahidul
• Format: Journal Article
• Language: English
• Published: England BioMed Central Ltd 29-04-2019; BioMed Central
• Subjects: Abiotic stress; Algorithms; Bark; Biochemistry; Biological research; Chromosomes, Plant - genetics; Corchorus - genetics; Criminal investigation; Cytochrome P-450; Deoxyribonucleic acid; DNA; Drought; Gene expression; Gene Expression Profiling; Gene Expression Regulation, Plant; Genes; Genetic aspects; Genetic engineering; Genetic regulation; Genetic research; Genomes; Genomics; Glyceraldehyde-3-phosphate dehydrogenase; Humidity; Identification and classification; Inoculation; Jute (Plant); Macrophomina phaseolina; Physiological aspects; Plant Components, Aerial - genetics; Plant development; Plant Roots - genetics; Polymerase chain reaction; Reference Standards; Reverse Transcriptase Polymerase Chain Reaction - methods; Reverse Transcriptase Polymerase Chain Reaction - standards; Reverse transcription; Ribonucleic acid; RNA; Salinity; Salinity effects; Seeds; Signal transduction; Sorghum; Studies; Textile fibers; Transcription (Genetics); Transcriptome; United States > US; Reference gene; Gene expression; qRT-PCR; Jute
• ISSN: 1471-2199; 1471-2199
• DOI: 10.1186/s12867-019-0130-2

With the availability of genome sequences, gene expression analysis of jute has drawn considerable attention for understanding the regulatory mechanisms of fiber development and improving fiber quality. Gene expression profiles of a target gene can provide valuable clues towards the understanding of its biological function. Reverse transcription quantitative real-time PCR (qRT-PCR) is the best method for targeted gene expression analysis due to its sensitivity and reproducibility. However, calculating relative expression requires reference genes, which must be stable across various biological conditions. For this purposes, 11 prospective genes namely, 28S RNA, ACT7, CYP, EF1A, EF2, ETIF3E, GAPDH, PP2Ac, PTB, UBC2 and UBI1 were evaluated for their potential use as reference genes in jute.
The expression stabilities of eleven prospective genes were analyzed in various jute plant tissues, such as the root, stick, bark, leaf, flower, seed and fiber, as well as under abiotic (waterlogged, drought and salinity) and biotic stress (infestation with Macrophomina phaseolina) conditions with different time points. All 11 genes were variably expressed in different tissues and stress conditions. To find suitable reference genes in different sample sets, a comprehensive approach based on four statistical algorithms such as GeNorm, BestKeeper, NormFinder the ΔCt was used. The PP2Ac and EF2 genes were the most stably expressed across the different tissues. ACT7 and UBC2 were suitable reference genes under drought stress, and CYP and PP2Ac were the most appropriate after inoculation with Macrophomina phaseolina. Under salinity stress, PP2Ac and UBC2 were the best genes, and ACT7 and PP2Ac were the most suitable under waterlogged conditions.
Expression stability of reference genes from jute varied in different tissues and selected experimental conditions. Our results provide a valuable resource for the accurate normalization of gene expression experiments in fiber research for important bast fiber crops.