Cargando…

Expression patterns of cysteine peptidase genes across the Tribolium castaneum life cycle provide clues to biological function

The red flour beetle, Tribolium castaneum, is a major agricultural pest responsible for considerable loss of stored grain and cereal products worldwide. T. castaneum larvae have a highly compartmentalized gut, with cysteine peptidases mostly in the acidic anterior part of the midgut that are critica...

Descripción completa

Detalles Bibliográficos
Autores principales: Perkin, Lindsey, Elpidina, Elena N., Oppert, Brenda
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PeerJ Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4727968/
https://www.ncbi.nlm.nih.gov/pubmed/26819843
http://dx.doi.org/10.7717/peerj.1581
_version_ 1782412049071996928
author Perkin, Lindsey
Elpidina, Elena N.
Oppert, Brenda
author_facet Perkin, Lindsey
Elpidina, Elena N.
Oppert, Brenda
author_sort Perkin, Lindsey
collection PubMed
description The red flour beetle, Tribolium castaneum, is a major agricultural pest responsible for considerable loss of stored grain and cereal products worldwide. T. castaneum larvae have a highly compartmentalized gut, with cysteine peptidases mostly in the acidic anterior part of the midgut that are critical to the early stages of food digestion. In previous studies, we described 26 putative cysteine peptidase genes in T. castaneum (types B, L, O, F, and K) located mostly on chromosomes 3, 7, 8, and 10. In the present study, we hypothesized that specific cysteine peptidase genes could be associated with digestive functions for food processing based on comparison of gene expression profiles in different developmental stages, feeding and non-feeding. RNA-Seq was used to determine the relative expression of cysteine peptidase genes among four major developmental stages (egg, larvae, pupae, and adult) of T. castaneum. We also compared cysteine peptidase genes in T. castaneum to those in other model insects and coleopteran pests. By combining transcriptome expression, phylogenetic comparisons, response to dietary inhibitors, and other existing data, we identified key cysteine peptidases that T. castaneum larvae and adults use for food digestion, and thus new potential targets for biologically-based control products.
format Online
Article
Text
id pubmed-4727968
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher PeerJ Inc.
record_format MEDLINE/PubMed
spelling pubmed-47279682016-01-27 Expression patterns of cysteine peptidase genes across the Tribolium castaneum life cycle provide clues to biological function Perkin, Lindsey Elpidina, Elena N. Oppert, Brenda PeerJ Agricultural Science The red flour beetle, Tribolium castaneum, is a major agricultural pest responsible for considerable loss of stored grain and cereal products worldwide. T. castaneum larvae have a highly compartmentalized gut, with cysteine peptidases mostly in the acidic anterior part of the midgut that are critical to the early stages of food digestion. In previous studies, we described 26 putative cysteine peptidase genes in T. castaneum (types B, L, O, F, and K) located mostly on chromosomes 3, 7, 8, and 10. In the present study, we hypothesized that specific cysteine peptidase genes could be associated with digestive functions for food processing based on comparison of gene expression profiles in different developmental stages, feeding and non-feeding. RNA-Seq was used to determine the relative expression of cysteine peptidase genes among four major developmental stages (egg, larvae, pupae, and adult) of T. castaneum. We also compared cysteine peptidase genes in T. castaneum to those in other model insects and coleopteran pests. By combining transcriptome expression, phylogenetic comparisons, response to dietary inhibitors, and other existing data, we identified key cysteine peptidases that T. castaneum larvae and adults use for food digestion, and thus new potential targets for biologically-based control products. PeerJ Inc. 2016-01-18 /pmc/articles/PMC4727968/ /pubmed/26819843 http://dx.doi.org/10.7717/peerj.1581 Text en http://creativecommons.org/publicdomain/zero/1.0/ This is an open access article, free of all copyright, made available under the Creative Commons Public Domain Dedication (http://creativecommons.org/publicdomain/zero/1.0/) . This work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose.
spellingShingle Agricultural Science
Perkin, Lindsey
Elpidina, Elena N.
Oppert, Brenda
Expression patterns of cysteine peptidase genes across the Tribolium castaneum life cycle provide clues to biological function
title Expression patterns of cysteine peptidase genes across the Tribolium castaneum life cycle provide clues to biological function
title_full Expression patterns of cysteine peptidase genes across the Tribolium castaneum life cycle provide clues to biological function
title_fullStr Expression patterns of cysteine peptidase genes across the Tribolium castaneum life cycle provide clues to biological function
title_full_unstemmed Expression patterns of cysteine peptidase genes across the Tribolium castaneum life cycle provide clues to biological function
title_short Expression patterns of cysteine peptidase genes across the Tribolium castaneum life cycle provide clues to biological function
title_sort expression patterns of cysteine peptidase genes across the tribolium castaneum life cycle provide clues to biological function
topic Agricultural Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4727968/
https://www.ncbi.nlm.nih.gov/pubmed/26819843
http://dx.doi.org/10.7717/peerj.1581
work_keys_str_mv AT perkinlindsey expressionpatternsofcysteinepeptidasegenesacrossthetriboliumcastaneumlifecycleprovidecluestobiologicalfunction
AT elpidinaelenan expressionpatternsofcysteinepeptidasegenesacrossthetriboliumcastaneumlifecycleprovidecluestobiologicalfunction
AT oppertbrenda expressionpatternsofcysteinepeptidasegenesacrossthetriboliumcastaneumlifecycleprovidecluestobiologicalfunction