Cargando…
Assessment and validation of a suite of reverse transcription-quantitative PCR reference genes for analyses of density-dependent behavioural plasticity in the Australian plague locust
BACKGROUND: The Australian plague locust, Chortoicetes terminifera, is among the most promising species to unravel the suites of genes underling the density-dependent shift from shy and cryptic solitarious behaviour to the highly active and aggregating gregarious behaviour that is characteristic of...
Autores principales: | , , , , , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2011
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3048552/ https://www.ncbi.nlm.nih.gov/pubmed/21324174 http://dx.doi.org/10.1186/1471-2199-12-7 |
_version_ | 1782199176079081472 |
---|---|
author | Chapuis, Marie-Pierre Tohidi-Esfahani, Donya Dodgson, Tim Blondin, Laurence Ponton, Fleur Cullen, Darron Simpson, Stephen J Sword, Gregory A |
author_facet | Chapuis, Marie-Pierre Tohidi-Esfahani, Donya Dodgson, Tim Blondin, Laurence Ponton, Fleur Cullen, Darron Simpson, Stephen J Sword, Gregory A |
author_sort | Chapuis, Marie-Pierre |
collection | PubMed |
description | BACKGROUND: The Australian plague locust, Chortoicetes terminifera, is among the most promising species to unravel the suites of genes underling the density-dependent shift from shy and cryptic solitarious behaviour to the highly active and aggregating gregarious behaviour that is characteristic of locusts. This is because it lacks many of the major phenotypic changes in colour and morphology that accompany phase change in other locust species. Reverse transcription-quantitative polymerase chain reaction (RT-qPCR) is the most sensitive method available for determining changes in gene expression. However, to accurately monitor the expression of target genes, it is essential to select an appropriate normalization strategy to control for non-specific variation between samples. Here we identify eight potential reference genes and examine their expression stability at different rearing density treatments in neural tissue of the Australian plague locust. RESULTS: Taking advantage of the new orthologous DNA sequences available in locusts, we developed primers for genes encoding 18SrRNA, ribosomal protein L32 (RpL32), armadillo (Arm), actin 5C (Actin), succinate dehydrogenase (SDHa), glyceraldehyde-3P-dehydrogenase (GAPDH), elongation factor 1 alpha (EF1a) and annexin IX (AnnIX). The relative transcription levels of these eight genes were then analyzed in three treatment groups differing in rearing density (isolated, short- and long-term crowded), each made up of five pools of four neural tissue samples from 5(th )instar nymphs. SDHa and GAPDH, which are both involved in metabolic pathways, were identified as the least stable in expression levels, challenging their usefulness in normalization. Based on calculations performed with the geNorm and NormFinder programs, the best combination of two genes for normalization of gene expression data following crowding in the Australian plague locust was EF1a and Arm. We applied their use to studying a target gene that encodes a Ca(2+ )binding glycoprotein, SPARC, which was previously found to be up-regulated in brains of gregarious desert locusts, Schistocerca gregaria. Interestingly, expression of this gene did not vary with rearing density in the same way in brains of the two locust species. Unlike S. gregaria, there was no effect of any crowding treatment in the Australian plague locust. CONCLUSION: Arm and EF1a is the most stably expressed combination of two reference genes of the eight examined for reliable normalization of RT-qPCR assays studying density-dependent behavioural change in the Australian plague locust. Such normalization allowed us to show that C. terminifera crowding did not change the neuronal expression of the SPARC gene, a gregarious phase-specific gene identified in brains of the desert locust, S. gregaria. Such comparative results on density-dependent gene regulation provide insights into the evolution of gregarious behaviour and mass migration of locusts. The eight identified genes we evaluated are also candidates as normalization genes for use in experiments involving other Oedipodinae species, but the rank order of gene stability must necessarily be determined on a case-by-case basis. |
format | Text |
id | pubmed-3048552 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-30485522011-03-05 Assessment and validation of a suite of reverse transcription-quantitative PCR reference genes for analyses of density-dependent behavioural plasticity in the Australian plague locust Chapuis, Marie-Pierre Tohidi-Esfahani, Donya Dodgson, Tim Blondin, Laurence Ponton, Fleur Cullen, Darron Simpson, Stephen J Sword, Gregory A BMC Mol Biol Research Article BACKGROUND: The Australian plague locust, Chortoicetes terminifera, is among the most promising species to unravel the suites of genes underling the density-dependent shift from shy and cryptic solitarious behaviour to the highly active and aggregating gregarious behaviour that is characteristic of locusts. This is because it lacks many of the major phenotypic changes in colour and morphology that accompany phase change in other locust species. Reverse transcription-quantitative polymerase chain reaction (RT-qPCR) is the most sensitive method available for determining changes in gene expression. However, to accurately monitor the expression of target genes, it is essential to select an appropriate normalization strategy to control for non-specific variation between samples. Here we identify eight potential reference genes and examine their expression stability at different rearing density treatments in neural tissue of the Australian plague locust. RESULTS: Taking advantage of the new orthologous DNA sequences available in locusts, we developed primers for genes encoding 18SrRNA, ribosomal protein L32 (RpL32), armadillo (Arm), actin 5C (Actin), succinate dehydrogenase (SDHa), glyceraldehyde-3P-dehydrogenase (GAPDH), elongation factor 1 alpha (EF1a) and annexin IX (AnnIX). The relative transcription levels of these eight genes were then analyzed in three treatment groups differing in rearing density (isolated, short- and long-term crowded), each made up of five pools of four neural tissue samples from 5(th )instar nymphs. SDHa and GAPDH, which are both involved in metabolic pathways, were identified as the least stable in expression levels, challenging their usefulness in normalization. Based on calculations performed with the geNorm and NormFinder programs, the best combination of two genes for normalization of gene expression data following crowding in the Australian plague locust was EF1a and Arm. We applied their use to studying a target gene that encodes a Ca(2+ )binding glycoprotein, SPARC, which was previously found to be up-regulated in brains of gregarious desert locusts, Schistocerca gregaria. Interestingly, expression of this gene did not vary with rearing density in the same way in brains of the two locust species. Unlike S. gregaria, there was no effect of any crowding treatment in the Australian plague locust. CONCLUSION: Arm and EF1a is the most stably expressed combination of two reference genes of the eight examined for reliable normalization of RT-qPCR assays studying density-dependent behavioural change in the Australian plague locust. Such normalization allowed us to show that C. terminifera crowding did not change the neuronal expression of the SPARC gene, a gregarious phase-specific gene identified in brains of the desert locust, S. gregaria. Such comparative results on density-dependent gene regulation provide insights into the evolution of gregarious behaviour and mass migration of locusts. The eight identified genes we evaluated are also candidates as normalization genes for use in experiments involving other Oedipodinae species, but the rank order of gene stability must necessarily be determined on a case-by-case basis. BioMed Central 2011-02-16 /pmc/articles/PMC3048552/ /pubmed/21324174 http://dx.doi.org/10.1186/1471-2199-12-7 Text en Copyright ©2011 Chapuis et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Chapuis, Marie-Pierre Tohidi-Esfahani, Donya Dodgson, Tim Blondin, Laurence Ponton, Fleur Cullen, Darron Simpson, Stephen J Sword, Gregory A Assessment and validation of a suite of reverse transcription-quantitative PCR reference genes for analyses of density-dependent behavioural plasticity in the Australian plague locust |
title | Assessment and validation of a suite of reverse transcription-quantitative PCR reference genes for analyses of density-dependent behavioural plasticity in the Australian plague locust |
title_full | Assessment and validation of a suite of reverse transcription-quantitative PCR reference genes for analyses of density-dependent behavioural plasticity in the Australian plague locust |
title_fullStr | Assessment and validation of a suite of reverse transcription-quantitative PCR reference genes for analyses of density-dependent behavioural plasticity in the Australian plague locust |
title_full_unstemmed | Assessment and validation of a suite of reverse transcription-quantitative PCR reference genes for analyses of density-dependent behavioural plasticity in the Australian plague locust |
title_short | Assessment and validation of a suite of reverse transcription-quantitative PCR reference genes for analyses of density-dependent behavioural plasticity in the Australian plague locust |
title_sort | assessment and validation of a suite of reverse transcription-quantitative pcr reference genes for analyses of density-dependent behavioural plasticity in the australian plague locust |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3048552/ https://www.ncbi.nlm.nih.gov/pubmed/21324174 http://dx.doi.org/10.1186/1471-2199-12-7 |
work_keys_str_mv | AT chapuismariepierre assessmentandvalidationofasuiteofreversetranscriptionquantitativepcrreferencegenesforanalysesofdensitydependentbehaviouralplasticityintheaustralianplaguelocust AT tohidiesfahanidonya assessmentandvalidationofasuiteofreversetranscriptionquantitativepcrreferencegenesforanalysesofdensitydependentbehaviouralplasticityintheaustralianplaguelocust AT dodgsontim assessmentandvalidationofasuiteofreversetranscriptionquantitativepcrreferencegenesforanalysesofdensitydependentbehaviouralplasticityintheaustralianplaguelocust AT blondinlaurence assessmentandvalidationofasuiteofreversetranscriptionquantitativepcrreferencegenesforanalysesofdensitydependentbehaviouralplasticityintheaustralianplaguelocust AT pontonfleur assessmentandvalidationofasuiteofreversetranscriptionquantitativepcrreferencegenesforanalysesofdensitydependentbehaviouralplasticityintheaustralianplaguelocust AT cullendarron assessmentandvalidationofasuiteofreversetranscriptionquantitativepcrreferencegenesforanalysesofdensitydependentbehaviouralplasticityintheaustralianplaguelocust AT simpsonstephenj assessmentandvalidationofasuiteofreversetranscriptionquantitativepcrreferencegenesforanalysesofdensitydependentbehaviouralplasticityintheaustralianplaguelocust AT swordgregorya assessmentandvalidationofasuiteofreversetranscriptionquantitativepcrreferencegenesforanalysesofdensitydependentbehaviouralplasticityintheaustralianplaguelocust |