Cargando…
Metabolomic insights into system-wide coordination of vertebrate metamorphosis
BACKGROUND: After completion of embryogenesis, many organisms experience an additional obligatory developmental transition to attain a substantially different juvenile or adult form. During anuran metamorphosis, the aquatic tadpole undergoes drastic morphological changes and remodelling of tissues a...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3928663/ https://www.ncbi.nlm.nih.gov/pubmed/24495308 http://dx.doi.org/10.1186/1471-213X-14-5 |
_version_ | 1782304296971272192 |
---|---|
author | Ichu, Taka-Aki Han, Jun Borchers, Christoph H Lesperance, Mary Helbing, Caren C |
author_facet | Ichu, Taka-Aki Han, Jun Borchers, Christoph H Lesperance, Mary Helbing, Caren C |
author_sort | Ichu, Taka-Aki |
collection | PubMed |
description | BACKGROUND: After completion of embryogenesis, many organisms experience an additional obligatory developmental transition to attain a substantially different juvenile or adult form. During anuran metamorphosis, the aquatic tadpole undergoes drastic morphological changes and remodelling of tissues and organs to become a froglet. Thyroid hormones are required to initiate the process, but the mechanism whereby the many requisite changes are coordinated between organs and tissues is poorly understood. Metabolites are often highly conserved biomolecules between species and are the closest reflection of phenotype. Due to the extensive distribution of blood throughout the organism, examination of the metabolites contained therein provides a system-wide overview of the coordinated changes experienced during metamorphosis. We performed an untargeted metabolomic analysis on serum samples from naturally-metamorphosing Rana catesbeiana from tadpoles to froglets using ultraperformance liquid chromatography coupled to a mass spectrometer. Total and aqueous metabolite extracts were obtained from each serum sample to select for nonpolar and polar metabolites, respectively, and selected metabolites were validated by running authentic compounds. RESULTS: The majority of the detected metabolites (74%) showed statistically significant abundance changes (p(adj) < 0.001) between metamorphic stages. We observed extensive remodelling of five core metabolic pathways: arginine and purine/pyrimidine, cysteine/methionine, sphingolipid, and eicosanoid metabolism and the urea cycle, and found evidence for a major role for lipids during this postembryonic process. Metabolites traditionally linked to human disease states were found to have biological linkages to the system-wide changes occuring during the events leading up to overt morphological change. CONCLUSIONS: To our knowledge, this is the first wide-scale metabolomic study of vertebrate metamorphosis identifying fundamental pathways involved in the coordination of this important developmental process and paves the way for metabolomic studies on other metamorphic systems including fish and insects. |
format | Online Article Text |
id | pubmed-3928663 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-39286632014-02-20 Metabolomic insights into system-wide coordination of vertebrate metamorphosis Ichu, Taka-Aki Han, Jun Borchers, Christoph H Lesperance, Mary Helbing, Caren C BMC Dev Biol Research Article BACKGROUND: After completion of embryogenesis, many organisms experience an additional obligatory developmental transition to attain a substantially different juvenile or adult form. During anuran metamorphosis, the aquatic tadpole undergoes drastic morphological changes and remodelling of tissues and organs to become a froglet. Thyroid hormones are required to initiate the process, but the mechanism whereby the many requisite changes are coordinated between organs and tissues is poorly understood. Metabolites are often highly conserved biomolecules between species and are the closest reflection of phenotype. Due to the extensive distribution of blood throughout the organism, examination of the metabolites contained therein provides a system-wide overview of the coordinated changes experienced during metamorphosis. We performed an untargeted metabolomic analysis on serum samples from naturally-metamorphosing Rana catesbeiana from tadpoles to froglets using ultraperformance liquid chromatography coupled to a mass spectrometer. Total and aqueous metabolite extracts were obtained from each serum sample to select for nonpolar and polar metabolites, respectively, and selected metabolites were validated by running authentic compounds. RESULTS: The majority of the detected metabolites (74%) showed statistically significant abundance changes (p(adj) < 0.001) between metamorphic stages. We observed extensive remodelling of five core metabolic pathways: arginine and purine/pyrimidine, cysteine/methionine, sphingolipid, and eicosanoid metabolism and the urea cycle, and found evidence for a major role for lipids during this postembryonic process. Metabolites traditionally linked to human disease states were found to have biological linkages to the system-wide changes occuring during the events leading up to overt morphological change. CONCLUSIONS: To our knowledge, this is the first wide-scale metabolomic study of vertebrate metamorphosis identifying fundamental pathways involved in the coordination of this important developmental process and paves the way for metabolomic studies on other metamorphic systems including fish and insects. BioMed Central 2014-02-05 /pmc/articles/PMC3928663/ /pubmed/24495308 http://dx.doi.org/10.1186/1471-213X-14-5 Text en Copyright © 2014 Ichu 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. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Ichu, Taka-Aki Han, Jun Borchers, Christoph H Lesperance, Mary Helbing, Caren C Metabolomic insights into system-wide coordination of vertebrate metamorphosis |
title | Metabolomic insights into system-wide coordination of vertebrate metamorphosis |
title_full | Metabolomic insights into system-wide coordination of vertebrate metamorphosis |
title_fullStr | Metabolomic insights into system-wide coordination of vertebrate metamorphosis |
title_full_unstemmed | Metabolomic insights into system-wide coordination of vertebrate metamorphosis |
title_short | Metabolomic insights into system-wide coordination of vertebrate metamorphosis |
title_sort | metabolomic insights into system-wide coordination of vertebrate metamorphosis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3928663/ https://www.ncbi.nlm.nih.gov/pubmed/24495308 http://dx.doi.org/10.1186/1471-213X-14-5 |
work_keys_str_mv | AT ichutakaaki metabolomicinsightsintosystemwidecoordinationofvertebratemetamorphosis AT hanjun metabolomicinsightsintosystemwidecoordinationofvertebratemetamorphosis AT borcherschristophh metabolomicinsightsintosystemwidecoordinationofvertebratemetamorphosis AT lesperancemary metabolomicinsightsintosystemwidecoordinationofvertebratemetamorphosis AT helbingcarenc metabolomicinsightsintosystemwidecoordinationofvertebratemetamorphosis |