Abstract

Selecting suitable internal reference genes is an important prerequisite for the application of quantitative real-time PCR (qRT-PCR). However, no systematic studies have been conducted on reference genes in luffa. In this study, seven reference genes were selected, and their expression levels in luffa plants exposed to various simulated abiotic stresses [i.e., cold, drought, heat, salt, H2O2, and abscisic acid (ABA) treatments] were analyzed by qRT-PCR. The stability of the reference gene expression levels was validated using the geNorm, NormFinder, BestKeeper, and RefFinder algorithms. The results indicated that EF-1α was the most stably expressed and suitable reference gene overall and for the heat, cold, and ABA treatments. Additionally, UBQ expression was stable following the salt treatment, whereas TUB was identified as a suitable reference gene for H2O2 and drought treatments. The reliability of the selected reference genes was verified by analyzing the expression of copper/zinc superoxide dismutase (Cu/Zn-SOD) gene in luffa. When the most unstable reference genes were used for data normalizations, the resulting expression patterns had obvious biases when compared with the expression patterns for the most ideal reference genes used alone or combined. These results will be conducive to more accurate quantification of gene expression levels in luffa.

Highlights

  • Selecting suitable internal reference genes is an important prerequisite for the application of quantitative real-time PCR

  • The TUB amino acid sequence was more than 96% identical to Cucumis sativus (XP_004139067.1), Momordica charantia (XP_022153267.1), and Brassica oleracea (VDD33972.1) sequences

  • The glyceraldehyde-3-phosphate dehydrogenase (GAPDH) amino acid sequence was more than 96% identical to Cucurbita moschata (XP_022937833.1), Cucumis melo (XP_008456541.1), and Momordica charantia (XP_022143215.1) sequences

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Summary

Introduction

Selecting suitable internal reference genes is an important prerequisite for the application of quantitative real-time PCR (qRT-PCR). Seven reference genes were selected, and their expression levels in luffa plants exposed to various simulated abiotic stresses [i.e., cold, drought, heat, salt, ­H2O2, and abscisic acid (ABA) treatments] were analyzed by qRT-PCR. Five common reference genes (ACT,TUA,TUB, EF-1α, and GAPDH) were cloned from luffa seedlings These genes along with two previously cloned reference genes, UBQ16 and 18S, were analyzed to identify the most reliable reference genes for normalizing target gene expression via qRT-PCR. To assess the utility of the validated reference genes, the expression levels of copper/zinc superoxide dismutase (Cu/Zn-SOD) gene under the above conditions were examined The results of these analyses may provide the basis for future qRT-PCR-based investigations of the transcription of important functional genes in luffa

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