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SSR marker development in Clerodendrum trichotomum using transcriptome sequencing

Clerodendrum trichotomum, a member of the Lamiaceae (Verbenaceae) family, is an ornamental plant widely distributed in South Asia. Previous studies have focused primarily on its growth characteristics, stress resistance, and pharmacological applications; however, molecular investigations remain limi...

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Autores principales: Chen, Gongwei, Yue, Yuanzheng, Hua, Yajie, Hu, Die, Shi, Tingting, Chang, Zhaojing, Yang, Xiulian, Wang, Lianggui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6867647/
https://www.ncbi.nlm.nih.gov/pubmed/31747430
http://dx.doi.org/10.1371/journal.pone.0225451
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author Chen, Gongwei
Yue, Yuanzheng
Hua, Yajie
Hu, Die
Shi, Tingting
Chang, Zhaojing
Yang, Xiulian
Wang, Lianggui
author_facet Chen, Gongwei
Yue, Yuanzheng
Hua, Yajie
Hu, Die
Shi, Tingting
Chang, Zhaojing
Yang, Xiulian
Wang, Lianggui
author_sort Chen, Gongwei
collection PubMed
description Clerodendrum trichotomum, a member of the Lamiaceae (Verbenaceae) family, is an ornamental plant widely distributed in South Asia. Previous studies have focused primarily on its growth characteristics, stress resistance, and pharmacological applications; however, molecular investigations remain limited. Considering germplasm conservation and the extensive applications of this plant, it is necessary to explore transcriptome resources and SSR makers for C. trichotomum. In the present study, RNA sequencing was used to determine the transcriptome of C. trichotomum. Subsequently, unigene annotations and classifications were obtained, and SSRs were mined with MIcroSAtellite. Finally, primer pairs designed with Oligo 6.0 were selected for polymorphism validation. In total, 127,325,666 high-quality reads were obtained, and 58,345 non-redundant unigenes were generated, of which 36,900 (63.24%) were annotated. Among the annotated unigenes, 35,980 (97.51%) had significant similarity to 607 species in Nr databases. In addition, a total of 6,444 SSRs were identified in 5,530 unigenes, and 200 random primer pairs were designed for polymorphism validation. Furthermore, after primary polymorphism identification, 30 polymorphic primer pairs were selected for the further polymorphism screening, and 200 alleles were identified, 197 of which showed polymorphism. In this work, a large number of unigenes were generated, and numerous SSRs were detected. These findings should be beneficial for further investigations into germplasm conservation and various applications of C. trichotomum. These results should also provide a solid foundation for future molecular biology studies in C. trichotomum.
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spelling pubmed-68676472019-12-07 SSR marker development in Clerodendrum trichotomum using transcriptome sequencing Chen, Gongwei Yue, Yuanzheng Hua, Yajie Hu, Die Shi, Tingting Chang, Zhaojing Yang, Xiulian Wang, Lianggui PLoS One Research Article Clerodendrum trichotomum, a member of the Lamiaceae (Verbenaceae) family, is an ornamental plant widely distributed in South Asia. Previous studies have focused primarily on its growth characteristics, stress resistance, and pharmacological applications; however, molecular investigations remain limited. Considering germplasm conservation and the extensive applications of this plant, it is necessary to explore transcriptome resources and SSR makers for C. trichotomum. In the present study, RNA sequencing was used to determine the transcriptome of C. trichotomum. Subsequently, unigene annotations and classifications were obtained, and SSRs were mined with MIcroSAtellite. Finally, primer pairs designed with Oligo 6.0 were selected for polymorphism validation. In total, 127,325,666 high-quality reads were obtained, and 58,345 non-redundant unigenes were generated, of which 36,900 (63.24%) were annotated. Among the annotated unigenes, 35,980 (97.51%) had significant similarity to 607 species in Nr databases. In addition, a total of 6,444 SSRs were identified in 5,530 unigenes, and 200 random primer pairs were designed for polymorphism validation. Furthermore, after primary polymorphism identification, 30 polymorphic primer pairs were selected for the further polymorphism screening, and 200 alleles were identified, 197 of which showed polymorphism. In this work, a large number of unigenes were generated, and numerous SSRs were detected. These findings should be beneficial for further investigations into germplasm conservation and various applications of C. trichotomum. These results should also provide a solid foundation for future molecular biology studies in C. trichotomum. Public Library of Science 2019-11-20 /pmc/articles/PMC6867647/ /pubmed/31747430 http://dx.doi.org/10.1371/journal.pone.0225451 Text en © 2019 Chen et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Chen, Gongwei
Yue, Yuanzheng
Hua, Yajie
Hu, Die
Shi, Tingting
Chang, Zhaojing
Yang, Xiulian
Wang, Lianggui
SSR marker development in Clerodendrum trichotomum using transcriptome sequencing
title SSR marker development in Clerodendrum trichotomum using transcriptome sequencing
title_full SSR marker development in Clerodendrum trichotomum using transcriptome sequencing
title_fullStr SSR marker development in Clerodendrum trichotomum using transcriptome sequencing
title_full_unstemmed SSR marker development in Clerodendrum trichotomum using transcriptome sequencing
title_short SSR marker development in Clerodendrum trichotomum using transcriptome sequencing
title_sort ssr marker development in clerodendrum trichotomum using transcriptome sequencing
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6867647/
https://www.ncbi.nlm.nih.gov/pubmed/31747430
http://dx.doi.org/10.1371/journal.pone.0225451
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