Stable reference genes for the measurement of transcript abundance during larval caste development in the honeybee

Many genes are differentially regulated by caste development in the honeybee. Identifying and understanding these differences is key to discovering the mechanisms underlying this process. To identify these gene expression differences requires robust methods to measure transcript abundance. RT-qPCR i...

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Published inApidologie Vol. 44; no. 4; pp. 357 - 366
Main Authors Cameron, Rosannah C, Duncan, Elizabeth J, Dearden, Peter K
Format Journal Article
LanguageEnglish
Published Paris Springer-Verlag 01.07.2013
EDP Sciences
Springer Verlag
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ISSN0044-8435
1297-9678
1297-9678
DOI10.1007/s13592-012-0187-0

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Abstract Many genes are differentially regulated by caste development in the honeybee. Identifying and understanding these differences is key to discovering the mechanisms underlying this process. To identify these gene expression differences requires robust methods to measure transcript abundance. RT-qPCR is currently the gold standard to measure gene expression, but requires stable reference genes to compare gene expression changes. Such reference genes have not been established for honeybee caste development. Here, we identify and test potential reference genes that have stable expression throughout larval development between the two female castes. In this study, 15 candidate reference genes were examined to identify the most stable reference genes. Three algorithms (GeNorm, Bestkeeper and NormFinder) were used to rank the candidate reference genes based on their stability between the castes throughout larval development. Of these genes Ndufa8 (the orthologue of a component of complex one of the mitochondrial electron transport chain) and Pros54 (orthologous to a component of the 26S proteasome) were identified as being the most stable. When these two genes were used to normalise expression of two target genes (previously found to be differentially expressed between queen and worker larvae by microarray analysis) they were able to more accurately detect differential expression than two previously used reference genes (awd and RpL12). The identification of these novel reference genes will be of benefit to future studies of caste development in the honeybee.
AbstractList Many genes are differentially regulated by caste development in the honeybee. Identifying and understanding these differences is key to discovering the mechanisms underlying this process. To identify these gene expression differences requires robust methods to measure transcript abundance. RT-qPCR is currently the gold standard to measure gene expression, but requires stable reference genes to compare gene expression changes. Such reference genes have not been established for honeybee caste development. Here, we identify and test potential reference genes that have stable expression throughout larval development between the two female castes. In this study, 15 candidate reference genes were examined to identify the most stable reference genes. Three algorithms (GeNorm, Bestkeeper and NormFinder) were used to rank the candidate reference genes based on their stability between the castes throughout larval development. Of these genes Ndufa8 (the orthologue of a component of complex one of the mitochondrial electron transport chain) and Pros54 (orthologous to a component of the 26S proteasome) were identified as being the most stable. When these two genes were used to normalise expression of two target genes (previously found to be differentially expressed between queen and worker larvae by microarray analysis) they were able to more accurately detect differential expression than two previously used reference genes ( awd and RpL12 ). The identification of these novel reference genes will be of benefit to future studies of caste development in the honeybee.
Many genes are differentially regulated by caste development in the honeybee. Identifying and understanding these differences is key to discovering the mechanisms underlying this process. To identify these gene expression differences requires robust methods to measure transcript abundance. RT-qPCR is currently the gold standard to measure gene expression, but requires stable reference genes to compare gene expression changes. Such reference genes have not been established for honeybee caste development. Here, we identify and test potential reference genes that have stable expression throughout larval development between the two female castes. In this study, 15 candidate reference genes were examined to identify the most stable reference genes. Three algorithms (GeNorm, Bestkeeper and NormFinder) were used to rank the candidate reference genes based on their stability between the castes throughout larval development. Of these genes Ndufa8 (the orthologue of a component of complex one of the mitochondrial electron transport chain) and Pros54 (orthologous to a component of the 26S proteasome) were identified as being the most stable. When these two genes were used to normalise expression of two target genes (previously found to be differentially expressed between queen and worker larvae by microarray analysis) they were able to more accurately detect differential expression than two previously used reference genes (awd and RpL12). The identification of these novel reference genes will be of benefit to future studies of caste development in the honeybee.
Author Cameron, Rosannah C
Duncan, Elizabeth J
Dearden, Peter K
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Issue 4
Keywords caste development
larval development
gene expression
Insecta
Apidae
Social insect
Gene expression
Apis mellifera
Apoidea
Arthropoda
Development
Caste
Intraspecific comparison
Hymenoptera
Invertebrata
Aculeata
Language English
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Snippet Many genes are differentially regulated by caste development in the honeybee. Identifying and understanding these differences is key to discovering the...
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StartPage 357
SubjectTerms Agricultural sciences
algorithms
Animal biology
Animal production studies
Animal productions
Apiculture
Biochemistry. Physiology. Immunology
Biodiversity
Biological and medical sciences
Biomedical and Life Sciences
Ecology, environment
electron transport chain
Entomology
Fundamental and applied biological sciences. Psychology
gene expression
gene expression regulation
genes
honey bees
Insecta
Invertebrate Zoology
Invertebrates
larvae
larval development
Life Sciences
microarray technology
Physiology. Development
proteasome endopeptidase complex
Terrestrial animal productions
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Title Stable reference genes for the measurement of transcript abundance during larval caste development in the honeybee
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