Abstract

BackgroundReal-time quantitative polymerase chain reaction (RT-qPCR) analysis is a low cost and sensitive technique that is widely used to measure levels of gene expression. Selecting and validating appropriate reference genes for normalising target gene expression should be the first step in any expression study to avoid inaccurate results.ResultsIn this study, ten candidate genes were tested for their suitability for use as reference genes in diurnal and developmental timecourse experiments in lettuce. The candidate reference genes were then used to normalise the expression pattern of the FLOWERING LOCUS T (FT) gene, one of key genes involved in the flowering time pathway whose expression is known to vary throughout the day and at different stages of development. Three reference genes, LsPP2A-1 (PROTEIN PHOSPHATASE 2A-1), LsPP2AA3 (PROTEIN PHOSPHATASE 2A REGULATORY SUBUNIT A3) and LsTIP41 (TAP42-INTERACTING PROTEIN OF 41 kDa), were the most stably expressed candidate reference genes throughout both the diurnal and developmental timecourse experiments. In the developmental experiment using just LsPP2A-1 and LsTIP41 as reference genes would be sufficient for accurate normalisation, whilst in the diurnal experiment all three reference genes, LsPP2A-1, LsPP2AA3 and LsTIP41, would be necessary. The FT expression pattern obtained demonstrates that the use of multiple and robust reference genes for RT-qPCR expression analyses results in a more accurate and reliable expression profile.ConclusionsReference genes suitable for use in diurnal and developmental timecourse experiments in lettuce were identified and used to produce a more accurate and reliable analysis of lsFT expression levels than previously obtained in such timecourse experiments.Electronic supplementary materialThe online version of this article (doi:10.1186/s13007-016-0121-y) contains supplementary material, which is available to authorized users.

Highlights

  • Real-time quantitative polymerase chain reaction (RT-qPCR) analysis is a low cost and sensitive technique that is widely used to measure levels of gene expression

  • A study investigated 17 selected candidate genes and microRNAs for their suitability to be used as reliable and stable reference genes in RTqPCR analysis of gene expression differences in abiotic stress experiments [10]. Some of these were genes such as TAP42-INTERACTING PROTEIN OF 41 kDa (TIP41), ADENOSINE PHOSPHORIBOSYL TRANSFERASE 1 (APT1) and miRNA genes and were selected on the basis that they had been used as reference genes in previously published work [2, 11,12,13]

  • In the present study a geNorm approach was used to investigate 10 candidate genes for their potential to be used as reference genes in diurnal and developmental time-course expression experiments in lettuce

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Summary

Introduction

Real-time quantitative polymerase chain reaction (RT-qPCR) analysis is a low cost and sensitive technique that is widely used to measure levels of gene expression. One of the most common techniques for studying gene expression is real-time quantitative polymerase chain reaction (RT-qPCR) analysis because it is extremely sensitive, specific and cost-effective. A study investigated 17 selected candidate genes and microRNAs (miRNAs) for their suitability to be used as reliable and stable reference genes in RTqPCR analysis of gene expression differences in abiotic stress experiments [10]. Some of these were genes such as TAP42-INTERACTING PROTEIN OF 41 kDa (TIP41), ADENOSINE PHOSPHORIBOSYL TRANSFERASE 1 (APT1) and miRNA genes and were selected on the basis that they had been used as reference genes in previously published work [2, 11,12,13]. In any RTqPCR experiment the identification of a good set of reference genes whose expression remains constant throughout the experimental conditions under study is extremely important in order to be able to obtain reliable results

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