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Identification of functional enolase genes of the silkworm Bombyx mori from public databases with a combination of dry and wet bench processes

BACKGROUND: Various insect species have been added to genomic databases over the years. Thus, researchers can easily obtain online genomic information on invertebrates and insects. However, many incorrectly annotated genes are included in these databases, which can prevent the correct interpretation...

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Autores principales: Kikuchi, Akira, Nakazato, Takeru, Ito, Katsuhiko, Nojima, Yosui, Yokoyama, Takeshi, Iwabuchi, Kikuo, Bono, Hidemasa, Toyoda, Atsushi, Fujiyama, Asao, Sato, Ryoichi, Tabunoki, Hiroko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5237310/
https://www.ncbi.nlm.nih.gov/pubmed/28086791
http://dx.doi.org/10.1186/s12864-016-3455-y
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author Kikuchi, Akira
Nakazato, Takeru
Ito, Katsuhiko
Nojima, Yosui
Yokoyama, Takeshi
Iwabuchi, Kikuo
Bono, Hidemasa
Toyoda, Atsushi
Fujiyama, Asao
Sato, Ryoichi
Tabunoki, Hiroko
author_facet Kikuchi, Akira
Nakazato, Takeru
Ito, Katsuhiko
Nojima, Yosui
Yokoyama, Takeshi
Iwabuchi, Kikuo
Bono, Hidemasa
Toyoda, Atsushi
Fujiyama, Asao
Sato, Ryoichi
Tabunoki, Hiroko
author_sort Kikuchi, Akira
collection PubMed
description BACKGROUND: Various insect species have been added to genomic databases over the years. Thus, researchers can easily obtain online genomic information on invertebrates and insects. However, many incorrectly annotated genes are included in these databases, which can prevent the correct interpretation of subsequent functional analyses. To address this problem, we used a combination of dry and wet bench processes to select functional genes from public databases. RESULTS: Enolase is an important glycolytic enzyme in all organisms. We used a combination of dry and wet bench processes to identify functional enolases in the silkworm Bombyx mori (BmEno). First, we detected five annotated enolases from public databases using a Hidden Markov Model (HMM) search, and then through cDNA cloning, Northern blotting, and RNA-seq analysis, we revealed three functional enolases in B. mori: BmEno1, BmEno2, and BmEnoC. BmEno1 contained a conserved key amino acid residue for metal binding and substrate binding in other species. However, BmEno2 and BmEnoC showed a change in this key amino acid. Phylogenetic analysis showed that BmEno2 and BmEnoC were distinct from BmEno1 and other enolases, and were distributed only in lepidopteran clusters. BmEno1 was expressed in all of the tissues used in our study. In contrast, BmEno2 was mainly expressed in the testis with some expression in the ovary and suboesophageal ganglion. BmEnoC was weakly expressed in the testis. Quantitative RT-PCR showed that the mRNA expression of BmEno2 and BmEnoC correlated with testis development; thus, BmEno2 and BmEnoC may be related to lepidopteran-specific spermiogenesis. CONCLUSIONS: We identified and characterized three functional enolases from public databases with a combination of dry and wet bench processes in the silkworm B. mori. In addition, we determined that BmEno2 and BmEnoC had species-specific functions. Our strategy could be helpful for the detection of minor genes and functional genes in non-model organisms from public databases. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-016-3455-y) contains supplementary material, which is available to authorized users.
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spelling pubmed-52373102017-01-18 Identification of functional enolase genes of the silkworm Bombyx mori from public databases with a combination of dry and wet bench processes Kikuchi, Akira Nakazato, Takeru Ito, Katsuhiko Nojima, Yosui Yokoyama, Takeshi Iwabuchi, Kikuo Bono, Hidemasa Toyoda, Atsushi Fujiyama, Asao Sato, Ryoichi Tabunoki, Hiroko BMC Genomics Research Article BACKGROUND: Various insect species have been added to genomic databases over the years. Thus, researchers can easily obtain online genomic information on invertebrates and insects. However, many incorrectly annotated genes are included in these databases, which can prevent the correct interpretation of subsequent functional analyses. To address this problem, we used a combination of dry and wet bench processes to select functional genes from public databases. RESULTS: Enolase is an important glycolytic enzyme in all organisms. We used a combination of dry and wet bench processes to identify functional enolases in the silkworm Bombyx mori (BmEno). First, we detected five annotated enolases from public databases using a Hidden Markov Model (HMM) search, and then through cDNA cloning, Northern blotting, and RNA-seq analysis, we revealed three functional enolases in B. mori: BmEno1, BmEno2, and BmEnoC. BmEno1 contained a conserved key amino acid residue for metal binding and substrate binding in other species. However, BmEno2 and BmEnoC showed a change in this key amino acid. Phylogenetic analysis showed that BmEno2 and BmEnoC were distinct from BmEno1 and other enolases, and were distributed only in lepidopteran clusters. BmEno1 was expressed in all of the tissues used in our study. In contrast, BmEno2 was mainly expressed in the testis with some expression in the ovary and suboesophageal ganglion. BmEnoC was weakly expressed in the testis. Quantitative RT-PCR showed that the mRNA expression of BmEno2 and BmEnoC correlated with testis development; thus, BmEno2 and BmEnoC may be related to lepidopteran-specific spermiogenesis. CONCLUSIONS: We identified and characterized three functional enolases from public databases with a combination of dry and wet bench processes in the silkworm B. mori. In addition, we determined that BmEno2 and BmEnoC had species-specific functions. Our strategy could be helpful for the detection of minor genes and functional genes in non-model organisms from public databases. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-016-3455-y) contains supplementary material, which is available to authorized users. BioMed Central 2017-01-13 /pmc/articles/PMC5237310/ /pubmed/28086791 http://dx.doi.org/10.1186/s12864-016-3455-y Text en © The Author(s). 2017 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
Kikuchi, Akira
Nakazato, Takeru
Ito, Katsuhiko
Nojima, Yosui
Yokoyama, Takeshi
Iwabuchi, Kikuo
Bono, Hidemasa
Toyoda, Atsushi
Fujiyama, Asao
Sato, Ryoichi
Tabunoki, Hiroko
Identification of functional enolase genes of the silkworm Bombyx mori from public databases with a combination of dry and wet bench processes
title Identification of functional enolase genes of the silkworm Bombyx mori from public databases with a combination of dry and wet bench processes
title_full Identification of functional enolase genes of the silkworm Bombyx mori from public databases with a combination of dry and wet bench processes
title_fullStr Identification of functional enolase genes of the silkworm Bombyx mori from public databases with a combination of dry and wet bench processes
title_full_unstemmed Identification of functional enolase genes of the silkworm Bombyx mori from public databases with a combination of dry and wet bench processes
title_short Identification of functional enolase genes of the silkworm Bombyx mori from public databases with a combination of dry and wet bench processes
title_sort identification of functional enolase genes of the silkworm bombyx mori from public databases with a combination of dry and wet bench processes
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5237310/
https://www.ncbi.nlm.nih.gov/pubmed/28086791
http://dx.doi.org/10.1186/s12864-016-3455-y
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