De Novo assembly, characterization and development of EST-SSRs from Bletilla striata transcriptomes profiled throughout the whole growing period.

Bletilla striata is an endangered orchid that has been used for millennia as a medicinal herb, in cosmetics and as a horticultural plant. To construct the first nucleotide database for this species and to develop abundant EST-SSR markers for facilitating further studies, various tissues and organs o...

Full description

Bibliographic Details
Main Authors: Delin Xu, Hongbo Chen, Murat Aci, Yinchi Pan, Yanni Shangguan, Jie Ma, Lin Li, Gang Qian, Qianxing Wang
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2018-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC6203367?pdf=render
id doaj-a97c1bc25eca4564a684274568b7cf87
record_format Article
spelling doaj-a97c1bc25eca4564a684274568b7cf872020-11-25T01:26:49ZengPublic Library of Science (PLoS)PLoS ONE1932-62032018-01-011310e020595410.1371/journal.pone.0205954De Novo assembly, characterization and development of EST-SSRs from Bletilla striata transcriptomes profiled throughout the whole growing period.Delin XuHongbo ChenMurat AciYinchi PanYanni ShangguanJie MaLin LiGang QianQianxing WangBletilla striata is an endangered orchid that has been used for millennia as a medicinal herb, in cosmetics and as a horticultural plant. To construct the first nucleotide database for this species and to develop abundant EST-SSR markers for facilitating further studies, various tissues and organs of plants in the main developmental stages were harvested for mRNA isolation and subsequent RNA sequencing. A total of 106,054,784 clean reads were generated by using Illumina paired-end sequencing technology. The reads were assembled into 127,261 unigenes by the Trinity package; the unigenes had an average length of 612 bp and an N50 of 957 bp. Of these unigenes, 67,494 (51.86%) were annotated in a series of databases. Of these annotated unigenes, 41,818 and 24,615 were assigned to gene ontology categories and clusters of orthologous groups, respectively. Additionally, 20,764 (15.96%) unigenes were mapped onto 275 pathways using the KEGG database. In addition, 25,935 high-quality EST-SSR primer pairs were developed from the 15,433 unigenes by MISA mining. To validate the accuracy of the newly designed markers, 87 of 100 randomly selected primers were effectively amplified; 63 of those yielded PCR products of the expected size, and 25 yielded products with significant amounts of polymorphism among the 4 landraces. Furthermore, the transferability test of the 25 polymorphic markers was performed in 6 individuals of two closely related genus Phalaenopsis and dendrobium. Which results showed a total of 5 markers can successfully amplified among these populations. This research provides a comprehensive nucleotide database and lays a solid foundation for functional gene mining and genomic research in B. striata. The developed EST-SSR primers could facilitate phylogenetic studies and breeding.http://europepmc.org/articles/PMC6203367?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Delin Xu
Hongbo Chen
Murat Aci
Yinchi Pan
Yanni Shangguan
Jie Ma
Lin Li
Gang Qian
Qianxing Wang
spellingShingle Delin Xu
Hongbo Chen
Murat Aci
Yinchi Pan
Yanni Shangguan
Jie Ma
Lin Li
Gang Qian
Qianxing Wang
De Novo assembly, characterization and development of EST-SSRs from Bletilla striata transcriptomes profiled throughout the whole growing period.
PLoS ONE
author_facet Delin Xu
Hongbo Chen
Murat Aci
Yinchi Pan
Yanni Shangguan
Jie Ma
Lin Li
Gang Qian
Qianxing Wang
author_sort Delin Xu
title De Novo assembly, characterization and development of EST-SSRs from Bletilla striata transcriptomes profiled throughout the whole growing period.
title_short De Novo assembly, characterization and development of EST-SSRs from Bletilla striata transcriptomes profiled throughout the whole growing period.
title_full De Novo assembly, characterization and development of EST-SSRs from Bletilla striata transcriptomes profiled throughout the whole growing period.
title_fullStr De Novo assembly, characterization and development of EST-SSRs from Bletilla striata transcriptomes profiled throughout the whole growing period.
title_full_unstemmed De Novo assembly, characterization and development of EST-SSRs from Bletilla striata transcriptomes profiled throughout the whole growing period.
title_sort de novo assembly, characterization and development of est-ssrs from bletilla striata transcriptomes profiled throughout the whole growing period.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2018-01-01
description Bletilla striata is an endangered orchid that has been used for millennia as a medicinal herb, in cosmetics and as a horticultural plant. To construct the first nucleotide database for this species and to develop abundant EST-SSR markers for facilitating further studies, various tissues and organs of plants in the main developmental stages were harvested for mRNA isolation and subsequent RNA sequencing. A total of 106,054,784 clean reads were generated by using Illumina paired-end sequencing technology. The reads were assembled into 127,261 unigenes by the Trinity package; the unigenes had an average length of 612 bp and an N50 of 957 bp. Of these unigenes, 67,494 (51.86%) were annotated in a series of databases. Of these annotated unigenes, 41,818 and 24,615 were assigned to gene ontology categories and clusters of orthologous groups, respectively. Additionally, 20,764 (15.96%) unigenes were mapped onto 275 pathways using the KEGG database. In addition, 25,935 high-quality EST-SSR primer pairs were developed from the 15,433 unigenes by MISA mining. To validate the accuracy of the newly designed markers, 87 of 100 randomly selected primers were effectively amplified; 63 of those yielded PCR products of the expected size, and 25 yielded products with significant amounts of polymorphism among the 4 landraces. Furthermore, the transferability test of the 25 polymorphic markers was performed in 6 individuals of two closely related genus Phalaenopsis and dendrobium. Which results showed a total of 5 markers can successfully amplified among these populations. This research provides a comprehensive nucleotide database and lays a solid foundation for functional gene mining and genomic research in B. striata. The developed EST-SSR primers could facilitate phylogenetic studies and breeding.
url http://europepmc.org/articles/PMC6203367?pdf=render
work_keys_str_mv AT delinxu denovoassemblycharacterizationanddevelopmentofestssrsfrombletillastriatatranscriptomesprofiledthroughoutthewholegrowingperiod
AT hongbochen denovoassemblycharacterizationanddevelopmentofestssrsfrombletillastriatatranscriptomesprofiledthroughoutthewholegrowingperiod
AT murataci denovoassemblycharacterizationanddevelopmentofestssrsfrombletillastriatatranscriptomesprofiledthroughoutthewholegrowingperiod
AT yinchipan denovoassemblycharacterizationanddevelopmentofestssrsfrombletillastriatatranscriptomesprofiledthroughoutthewholegrowingperiod
AT yannishangguan denovoassemblycharacterizationanddevelopmentofestssrsfrombletillastriatatranscriptomesprofiledthroughoutthewholegrowingperiod
AT jiema denovoassemblycharacterizationanddevelopmentofestssrsfrombletillastriatatranscriptomesprofiledthroughoutthewholegrowingperiod
AT linli denovoassemblycharacterizationanddevelopmentofestssrsfrombletillastriatatranscriptomesprofiledthroughoutthewholegrowingperiod
AT gangqian denovoassemblycharacterizationanddevelopmentofestssrsfrombletillastriatatranscriptomesprofiledthroughoutthewholegrowingperiod
AT qianxingwang denovoassemblycharacterizationanddevelopmentofestssrsfrombletillastriatatranscriptomesprofiledthroughoutthewholegrowingperiod
_version_ 1725108841203367936