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Moult cycle specific differential gene expression profiling of the crab Portunus pelagicus

BACKGROUND: Crustacean moulting is a complex process involving many regulatory pathways. A holistic approach to examine differential gene expression profiles of transcripts relevant to the moulting process, across all moult cycle stages, was used in this study. Custom cDNA microarrays were construct...

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Autores principales: Kuballa, Anna V, Holton, Timothy A, Paterson, Brian, Elizur, Abigail
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3062621/
https://www.ncbi.nlm.nih.gov/pubmed/21396120
http://dx.doi.org/10.1186/1471-2164-12-147
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author Kuballa, Anna V
Holton, Timothy A
Paterson, Brian
Elizur, Abigail
author_facet Kuballa, Anna V
Holton, Timothy A
Paterson, Brian
Elizur, Abigail
author_sort Kuballa, Anna V
collection PubMed
description BACKGROUND: Crustacean moulting is a complex process involving many regulatory pathways. A holistic approach to examine differential gene expression profiles of transcripts relevant to the moulting process, across all moult cycle stages, was used in this study. Custom cDNA microarrays were constructed for Portunus pelagicus. The printed arrays contained 5000 transcripts derived from both the whole organism, and from individual organs such as the brain, eyestalk, mandibular organ and Y-organ from all moult cycle stages. RESULTS: A total of 556 clones were sequenced from the cDNA libraries used to construct the arrays. These cDNAs represented 175 singletons and 62 contigs, resulting in 237 unique putative genes. The gene sequences were classified into the following biological functions: cuticular proteins associated with arthropod exoskeletons, farnesoic acid O-methyltransferase (FaMeT), proteins belonging to the hemocyanin gene family, lectins, proteins relevant to lipid metabolism, mitochondrial proteins, muscle related proteins, phenoloxidase activators and ribosomal proteins. Moult cycle-related differential expression patterns were observed for many transcripts. Of particular interest were those relating to the formation and hardening of the exoskeleton, and genes associated with cell respiration and energy metabolism. CONCLUSIONS: The expression data presented here provide a chronological depiction of the molecular events associated with the biological changes that occur during the crustacean moult cycle. Tracing the temporal expression patterns of a large variety of transcripts involved in the moult cycle of P. pelagicus can provide a greater understanding of gene function, interaction, and regulation of both known and new genes with respect to the moulting process.
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spelling pubmed-30626212011-03-23 Moult cycle specific differential gene expression profiling of the crab Portunus pelagicus Kuballa, Anna V Holton, Timothy A Paterson, Brian Elizur, Abigail BMC Genomics Research Article BACKGROUND: Crustacean moulting is a complex process involving many regulatory pathways. A holistic approach to examine differential gene expression profiles of transcripts relevant to the moulting process, across all moult cycle stages, was used in this study. Custom cDNA microarrays were constructed for Portunus pelagicus. The printed arrays contained 5000 transcripts derived from both the whole organism, and from individual organs such as the brain, eyestalk, mandibular organ and Y-organ from all moult cycle stages. RESULTS: A total of 556 clones were sequenced from the cDNA libraries used to construct the arrays. These cDNAs represented 175 singletons and 62 contigs, resulting in 237 unique putative genes. The gene sequences were classified into the following biological functions: cuticular proteins associated with arthropod exoskeletons, farnesoic acid O-methyltransferase (FaMeT), proteins belonging to the hemocyanin gene family, lectins, proteins relevant to lipid metabolism, mitochondrial proteins, muscle related proteins, phenoloxidase activators and ribosomal proteins. Moult cycle-related differential expression patterns were observed for many transcripts. Of particular interest were those relating to the formation and hardening of the exoskeleton, and genes associated with cell respiration and energy metabolism. CONCLUSIONS: The expression data presented here provide a chronological depiction of the molecular events associated with the biological changes that occur during the crustacean moult cycle. Tracing the temporal expression patterns of a large variety of transcripts involved in the moult cycle of P. pelagicus can provide a greater understanding of gene function, interaction, and regulation of both known and new genes with respect to the moulting process. BioMed Central 2011-03-12 /pmc/articles/PMC3062621/ /pubmed/21396120 http://dx.doi.org/10.1186/1471-2164-12-147 Text en Copyright ©2011 Kuballa 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
Kuballa, Anna V
Holton, Timothy A
Paterson, Brian
Elizur, Abigail
Moult cycle specific differential gene expression profiling of the crab Portunus pelagicus
title Moult cycle specific differential gene expression profiling of the crab Portunus pelagicus
title_full Moult cycle specific differential gene expression profiling of the crab Portunus pelagicus
title_fullStr Moult cycle specific differential gene expression profiling of the crab Portunus pelagicus
title_full_unstemmed Moult cycle specific differential gene expression profiling of the crab Portunus pelagicus
title_short Moult cycle specific differential gene expression profiling of the crab Portunus pelagicus
title_sort moult cycle specific differential gene expression profiling of the crab portunus pelagicus
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3062621/
https://www.ncbi.nlm.nih.gov/pubmed/21396120
http://dx.doi.org/10.1186/1471-2164-12-147
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