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Transcriptome profiling of differentially expressed genes in floral buds and flowers of male sterile and fertile lines in watermelon

BACKGROUND: Male sterility is an important mechanism for the production of hybrid seeds in watermelon. Although fruit development has been studied extensively in watermelon, there are no reports on gene expression in floral organs. In this study, RNA-sequencing (RNA-seq) was performed in two near-is...

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Autores principales: Rhee, Sun-Ju, Seo, Minseok, Jang, Yoon-Jeong, Cho, Seoae, Lee, Gung Pyo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4640349/
https://www.ncbi.nlm.nih.gov/pubmed/26552448
http://dx.doi.org/10.1186/s12864-015-2186-9
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author Rhee, Sun-Ju
Seo, Minseok
Jang, Yoon-Jeong
Cho, Seoae
Lee, Gung Pyo
author_facet Rhee, Sun-Ju
Seo, Minseok
Jang, Yoon-Jeong
Cho, Seoae
Lee, Gung Pyo
author_sort Rhee, Sun-Ju
collection PubMed
description BACKGROUND: Male sterility is an important mechanism for the production of hybrid seeds in watermelon. Although fruit development has been studied extensively in watermelon, there are no reports on gene expression in floral organs. In this study, RNA-sequencing (RNA-seq) was performed in two near-isogenic watermelon lines (genic male sterile [GMS] line, DAH3615-MS and male fertile line, DAH3615) to identify the differentially expressed genes (DEGs) related to male sterility. RESULTS: DEG analysis showed that 1259 genes were significantly associated with male sterility at a FDR P-value of < 0.01. Most of these genes were only expressed in the male fertile line. In addition, 11 functional clusters were identified using DAVID functional classification analysis. Of detected genes in RNA-seq analysis, 19 were successfully validated by qRT-PCR. CONCLUSIONS: In this study, we carried out a comprehensive floral transcriptome sequence comparison of a male fertile line and its near-isogenic male sterile line in watermelon. This analysis revealed essential genes responsible for stamen development, including pollen development and pollen tube elongation, and allowed their functional classification. These results provided new information on global mechanisms related to male sterility in watermelon. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-015-2186-9) contains supplementary material, which is available to authorized users.
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spelling pubmed-46403492015-11-11 Transcriptome profiling of differentially expressed genes in floral buds and flowers of male sterile and fertile lines in watermelon Rhee, Sun-Ju Seo, Minseok Jang, Yoon-Jeong Cho, Seoae Lee, Gung Pyo BMC Genomics Research Article BACKGROUND: Male sterility is an important mechanism for the production of hybrid seeds in watermelon. Although fruit development has been studied extensively in watermelon, there are no reports on gene expression in floral organs. In this study, RNA-sequencing (RNA-seq) was performed in two near-isogenic watermelon lines (genic male sterile [GMS] line, DAH3615-MS and male fertile line, DAH3615) to identify the differentially expressed genes (DEGs) related to male sterility. RESULTS: DEG analysis showed that 1259 genes were significantly associated with male sterility at a FDR P-value of < 0.01. Most of these genes were only expressed in the male fertile line. In addition, 11 functional clusters were identified using DAVID functional classification analysis. Of detected genes in RNA-seq analysis, 19 were successfully validated by qRT-PCR. CONCLUSIONS: In this study, we carried out a comprehensive floral transcriptome sequence comparison of a male fertile line and its near-isogenic male sterile line in watermelon. This analysis revealed essential genes responsible for stamen development, including pollen development and pollen tube elongation, and allowed their functional classification. These results provided new information on global mechanisms related to male sterility in watermelon. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-015-2186-9) contains supplementary material, which is available to authorized users. BioMed Central 2015-11-09 /pmc/articles/PMC4640349/ /pubmed/26552448 http://dx.doi.org/10.1186/s12864-015-2186-9 Text en © Rhee et al. 2015 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
Rhee, Sun-Ju
Seo, Minseok
Jang, Yoon-Jeong
Cho, Seoae
Lee, Gung Pyo
Transcriptome profiling of differentially expressed genes in floral buds and flowers of male sterile and fertile lines in watermelon
title Transcriptome profiling of differentially expressed genes in floral buds and flowers of male sterile and fertile lines in watermelon
title_full Transcriptome profiling of differentially expressed genes in floral buds and flowers of male sterile and fertile lines in watermelon
title_fullStr Transcriptome profiling of differentially expressed genes in floral buds and flowers of male sterile and fertile lines in watermelon
title_full_unstemmed Transcriptome profiling of differentially expressed genes in floral buds and flowers of male sterile and fertile lines in watermelon
title_short Transcriptome profiling of differentially expressed genes in floral buds and flowers of male sterile and fertile lines in watermelon
title_sort transcriptome profiling of differentially expressed genes in floral buds and flowers of male sterile and fertile lines in watermelon
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4640349/
https://www.ncbi.nlm.nih.gov/pubmed/26552448
http://dx.doi.org/10.1186/s12864-015-2186-9
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