Cargando…
Screening Potential Reference Genes in Tuta absoluta with Real-Time Quantitative PCR Analysis under Different Experimental Conditions
Tuta absoluta is one of the most significant invasive pests affecting tomato plants worldwide. RT-qPCR has emerged as one of the most sensitive and accurate methods for detecting gene expression data. The screening of stable internal reference genes is the most critical step for studying the molecul...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8391263/ https://www.ncbi.nlm.nih.gov/pubmed/34440427 http://dx.doi.org/10.3390/genes12081253 |
_version_ | 1783743234029125632 |
---|---|
author | Yang, An-Pei Wang, Yu-Sheng Huang, Cong Lv, Zhi-Chuang Liu, Wan-Xue Bi, Si-Yan Wan, Fang-Hao Wu, Qiang Zhang, Gui-Fen |
author_facet | Yang, An-Pei Wang, Yu-Sheng Huang, Cong Lv, Zhi-Chuang Liu, Wan-Xue Bi, Si-Yan Wan, Fang-Hao Wu, Qiang Zhang, Gui-Fen |
author_sort | Yang, An-Pei |
collection | PubMed |
description | Tuta absoluta is one of the most significant invasive pests affecting tomato plants worldwide. RT-qPCR has emerged as one of the most sensitive and accurate methods for detecting gene expression data. The screening of stable internal reference genes is the most critical step for studying the molecular mechanisms of environmental adaptability. The stable reference genes expressed in T. absoluta under specific experimental conditions have not yet been clarified. In this study, seven candidate reference genes (RPL27, RPS13, RPS15, EF1-α, TUB, TBP, and β-actin) and their optimal numbers were evaluated under biotic (developmental stages and adult tissues) and abiotic (insecticide, temperature, and plant VOC) conditions using four software programs. Our results identified the following reference genes and numbers as optimal: three genes (EF1-α, RPS13, and RPL27) for different developmental stages (egg, larva, pupa, unmated adult), two genes (RPS13 and TBP) for adult tissues (antenna, head, thorax, abdomen, leg), two genes (TBP and RPS13) for insecticides (Bacillus thuringiensis, chlorpyrifos, abamectin-aminomethyl, and chlorantraniliprole), two genes (RPL27 and TUB) for temperature-induced stresses (0, 25, and 40 °C), and two genes (RPS13 and TUB) for VOC-induced stresses (nonanal, α-phellandrene, and tomato leaves). Our results provide a reference for selecting appropriate reference genes for further study of the functional genes of T. absoluta under different experimental conditions. |
format | Online Article Text |
id | pubmed-8391263 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-83912632021-08-28 Screening Potential Reference Genes in Tuta absoluta with Real-Time Quantitative PCR Analysis under Different Experimental Conditions Yang, An-Pei Wang, Yu-Sheng Huang, Cong Lv, Zhi-Chuang Liu, Wan-Xue Bi, Si-Yan Wan, Fang-Hao Wu, Qiang Zhang, Gui-Fen Genes (Basel) Article Tuta absoluta is one of the most significant invasive pests affecting tomato plants worldwide. RT-qPCR has emerged as one of the most sensitive and accurate methods for detecting gene expression data. The screening of stable internal reference genes is the most critical step for studying the molecular mechanisms of environmental adaptability. The stable reference genes expressed in T. absoluta under specific experimental conditions have not yet been clarified. In this study, seven candidate reference genes (RPL27, RPS13, RPS15, EF1-α, TUB, TBP, and β-actin) and their optimal numbers were evaluated under biotic (developmental stages and adult tissues) and abiotic (insecticide, temperature, and plant VOC) conditions using four software programs. Our results identified the following reference genes and numbers as optimal: three genes (EF1-α, RPS13, and RPL27) for different developmental stages (egg, larva, pupa, unmated adult), two genes (RPS13 and TBP) for adult tissues (antenna, head, thorax, abdomen, leg), two genes (TBP and RPS13) for insecticides (Bacillus thuringiensis, chlorpyrifos, abamectin-aminomethyl, and chlorantraniliprole), two genes (RPL27 and TUB) for temperature-induced stresses (0, 25, and 40 °C), and two genes (RPS13 and TUB) for VOC-induced stresses (nonanal, α-phellandrene, and tomato leaves). Our results provide a reference for selecting appropriate reference genes for further study of the functional genes of T. absoluta under different experimental conditions. MDPI 2021-08-17 /pmc/articles/PMC8391263/ /pubmed/34440427 http://dx.doi.org/10.3390/genes12081253 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Yang, An-Pei Wang, Yu-Sheng Huang, Cong Lv, Zhi-Chuang Liu, Wan-Xue Bi, Si-Yan Wan, Fang-Hao Wu, Qiang Zhang, Gui-Fen Screening Potential Reference Genes in Tuta absoluta with Real-Time Quantitative PCR Analysis under Different Experimental Conditions |
title | Screening Potential Reference Genes in Tuta absoluta with Real-Time Quantitative PCR Analysis under Different Experimental Conditions |
title_full | Screening Potential Reference Genes in Tuta absoluta with Real-Time Quantitative PCR Analysis under Different Experimental Conditions |
title_fullStr | Screening Potential Reference Genes in Tuta absoluta with Real-Time Quantitative PCR Analysis under Different Experimental Conditions |
title_full_unstemmed | Screening Potential Reference Genes in Tuta absoluta with Real-Time Quantitative PCR Analysis under Different Experimental Conditions |
title_short | Screening Potential Reference Genes in Tuta absoluta with Real-Time Quantitative PCR Analysis under Different Experimental Conditions |
title_sort | screening potential reference genes in tuta absoluta with real-time quantitative pcr analysis under different experimental conditions |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8391263/ https://www.ncbi.nlm.nih.gov/pubmed/34440427 http://dx.doi.org/10.3390/genes12081253 |
work_keys_str_mv | AT yanganpei screeningpotentialreferencegenesintutaabsolutawithrealtimequantitativepcranalysisunderdifferentexperimentalconditions AT wangyusheng screeningpotentialreferencegenesintutaabsolutawithrealtimequantitativepcranalysisunderdifferentexperimentalconditions AT huangcong screeningpotentialreferencegenesintutaabsolutawithrealtimequantitativepcranalysisunderdifferentexperimentalconditions AT lvzhichuang screeningpotentialreferencegenesintutaabsolutawithrealtimequantitativepcranalysisunderdifferentexperimentalconditions AT liuwanxue screeningpotentialreferencegenesintutaabsolutawithrealtimequantitativepcranalysisunderdifferentexperimentalconditions AT bisiyan screeningpotentialreferencegenesintutaabsolutawithrealtimequantitativepcranalysisunderdifferentexperimentalconditions AT wanfanghao screeningpotentialreferencegenesintutaabsolutawithrealtimequantitativepcranalysisunderdifferentexperimentalconditions AT wuqiang screeningpotentialreferencegenesintutaabsolutawithrealtimequantitativepcranalysisunderdifferentexperimentalconditions AT zhangguifen screeningpotentialreferencegenesintutaabsolutawithrealtimequantitativepcranalysisunderdifferentexperimentalconditions |