Cargando…

Transcriptome analysis reveals the genetic basis underlying the seasonal development of keratinized nuptial spines in Leptobrachium boringii

BACKGROUND: The expression of sexually selected traits often varies with populations’ breeding cycles in many animals. The elucidation of mechanisms underlying the expression of such traits is a research topic in evolutionary biology; however, the genetic basis of the seasonal development of their e...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhang, Wei, Guo, Yue, Li, Jun, Huang, Li, Kazitsa, Eric Gilbert, Wu, Hua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5126826/
https://www.ncbi.nlm.nih.gov/pubmed/27894252
http://dx.doi.org/10.1186/s12864-016-3295-9
_version_ 1782470176888848384
author Zhang, Wei
Guo, Yue
Li, Jun
Huang, Li
Kazitsa, Eric Gilbert
Wu, Hua
author_facet Zhang, Wei
Guo, Yue
Li, Jun
Huang, Li
Kazitsa, Eric Gilbert
Wu, Hua
author_sort Zhang, Wei
collection PubMed
description BACKGROUND: The expression of sexually selected traits often varies with populations’ breeding cycles in many animals. The elucidation of mechanisms underlying the expression of such traits is a research topic in evolutionary biology; however, the genetic basis of the seasonal development of their expression remains unknown. Male Leptobrachium boringii develop keratinized nuptial spines on their upper jaw during the breeding season that fall off when the breeding season ends. To illuminate the genetic basis for the expression of this trait and its seasonal development, we assessed the de novo transcriptome for L. boringii using brain, testis and upper jaw skin and compared gene expression profiles of these tissues between two critical periods of the spine growth cycle. RESULTS: We identified 94,900 unigenes in our transcriptome. Among them, 2,131 genes were differentially expressed between the breeding period when the spines developed and the post-breeding period when the spines were sloughed. An increased number of differentially expressed genes (DEGs) were identified in the upper jaw skin compared with the testis and brain. In the upper jaw skin, DEGs were mainly enriched in cytosolic part, peptidase inhibitor activity and peptidase regulator activity based on GO enrichment analysis and in glycolysis/gluconeogenesis, ribosome biogenesis in eukaryotes and retinol metabolism based on KEGG enrichment analysis. In the other two tissues, DEGs were primarily involved in the cell cycle, DNA replication and melatonin production. Specifically, insulin/insulin-like growth factor and sex steroid hormone-related DEGs were identified in the upper jaw skin, indicating . The expression variation of IGF2 and estrogen-related genes may be the main factors regulating the seasonal development of the spines. CONCLUSIONS: Our study provides a list of potential genes involved in the regulation of seasonal development of nuptial spines in L. boringii. This is the first transcriptome survey of seasonally developed sexually selected traits for non-model amphibian species, and candidate genes provided here may provide valuable information for further studies of L. boringii. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-016-3295-9) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-5126826
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-51268262016-12-08 Transcriptome analysis reveals the genetic basis underlying the seasonal development of keratinized nuptial spines in Leptobrachium boringii Zhang, Wei Guo, Yue Li, Jun Huang, Li Kazitsa, Eric Gilbert Wu, Hua BMC Genomics Research Article BACKGROUND: The expression of sexually selected traits often varies with populations’ breeding cycles in many animals. The elucidation of mechanisms underlying the expression of such traits is a research topic in evolutionary biology; however, the genetic basis of the seasonal development of their expression remains unknown. Male Leptobrachium boringii develop keratinized nuptial spines on their upper jaw during the breeding season that fall off when the breeding season ends. To illuminate the genetic basis for the expression of this trait and its seasonal development, we assessed the de novo transcriptome for L. boringii using brain, testis and upper jaw skin and compared gene expression profiles of these tissues between two critical periods of the spine growth cycle. RESULTS: We identified 94,900 unigenes in our transcriptome. Among them, 2,131 genes were differentially expressed between the breeding period when the spines developed and the post-breeding period when the spines were sloughed. An increased number of differentially expressed genes (DEGs) were identified in the upper jaw skin compared with the testis and brain. In the upper jaw skin, DEGs were mainly enriched in cytosolic part, peptidase inhibitor activity and peptidase regulator activity based on GO enrichment analysis and in glycolysis/gluconeogenesis, ribosome biogenesis in eukaryotes and retinol metabolism based on KEGG enrichment analysis. In the other two tissues, DEGs were primarily involved in the cell cycle, DNA replication and melatonin production. Specifically, insulin/insulin-like growth factor and sex steroid hormone-related DEGs were identified in the upper jaw skin, indicating . The expression variation of IGF2 and estrogen-related genes may be the main factors regulating the seasonal development of the spines. CONCLUSIONS: Our study provides a list of potential genes involved in the regulation of seasonal development of nuptial spines in L. boringii. This is the first transcriptome survey of seasonally developed sexually selected traits for non-model amphibian species, and candidate genes provided here may provide valuable information for further studies of L. boringii. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-016-3295-9) contains supplementary material, which is available to authorized users. BioMed Central 2016-11-28 /pmc/articles/PMC5126826/ /pubmed/27894252 http://dx.doi.org/10.1186/s12864-016-3295-9 Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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
Zhang, Wei
Guo, Yue
Li, Jun
Huang, Li
Kazitsa, Eric Gilbert
Wu, Hua
Transcriptome analysis reveals the genetic basis underlying the seasonal development of keratinized nuptial spines in Leptobrachium boringii
title Transcriptome analysis reveals the genetic basis underlying the seasonal development of keratinized nuptial spines in Leptobrachium boringii
title_full Transcriptome analysis reveals the genetic basis underlying the seasonal development of keratinized nuptial spines in Leptobrachium boringii
title_fullStr Transcriptome analysis reveals the genetic basis underlying the seasonal development of keratinized nuptial spines in Leptobrachium boringii
title_full_unstemmed Transcriptome analysis reveals the genetic basis underlying the seasonal development of keratinized nuptial spines in Leptobrachium boringii
title_short Transcriptome analysis reveals the genetic basis underlying the seasonal development of keratinized nuptial spines in Leptobrachium boringii
title_sort transcriptome analysis reveals the genetic basis underlying the seasonal development of keratinized nuptial spines in leptobrachium boringii
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5126826/
https://www.ncbi.nlm.nih.gov/pubmed/27894252
http://dx.doi.org/10.1186/s12864-016-3295-9
work_keys_str_mv AT zhangwei transcriptomeanalysisrevealsthegeneticbasisunderlyingtheseasonaldevelopmentofkeratinizednuptialspinesinleptobrachiumboringii
AT guoyue transcriptomeanalysisrevealsthegeneticbasisunderlyingtheseasonaldevelopmentofkeratinizednuptialspinesinleptobrachiumboringii
AT lijun transcriptomeanalysisrevealsthegeneticbasisunderlyingtheseasonaldevelopmentofkeratinizednuptialspinesinleptobrachiumboringii
AT huangli transcriptomeanalysisrevealsthegeneticbasisunderlyingtheseasonaldevelopmentofkeratinizednuptialspinesinleptobrachiumboringii
AT kazitsaericgilbert transcriptomeanalysisrevealsthegeneticbasisunderlyingtheseasonaldevelopmentofkeratinizednuptialspinesinleptobrachiumboringii
AT wuhua transcriptomeanalysisrevealsthegeneticbasisunderlyingtheseasonaldevelopmentofkeratinizednuptialspinesinleptobrachiumboringii