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Characterization of the Lycium barbarum fruit transcriptome and development of EST-SSR markers

Lycium barbarum, commonly known as goji, is important in Chinese herbal medicine and its fruit is a very important agricultural and biological product. However, the molecular mechanism of formation of its fruit and associated medicinal and nutritional components is unexplored. Moreover, this species...

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Autores principales: Chen, Chunling, Xu, Meilong, Wang, Cuiping, Qiao, Gaixia, Wang, Wenwen, Tan, Zhaoyun, Wu, Tiantian, Zhang, Zhengsheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5695279/
https://www.ncbi.nlm.nih.gov/pubmed/29125846
http://dx.doi.org/10.1371/journal.pone.0187738
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author Chen, Chunling
Xu, Meilong
Wang, Cuiping
Qiao, Gaixia
Wang, Wenwen
Tan, Zhaoyun
Wu, Tiantian
Zhang, Zhengsheng
author_facet Chen, Chunling
Xu, Meilong
Wang, Cuiping
Qiao, Gaixia
Wang, Wenwen
Tan, Zhaoyun
Wu, Tiantian
Zhang, Zhengsheng
author_sort Chen, Chunling
collection PubMed
description Lycium barbarum, commonly known as goji, is important in Chinese herbal medicine and its fruit is a very important agricultural and biological product. However, the molecular mechanism of formation of its fruit and associated medicinal and nutritional components is unexplored. Moreover, this species lacks SSR markers due to lack of genomic and transcriptomic information. In this study, a total of 139,333 unigenes with average length of 1049 bp and N50 of 1579 bp are obtained by trinity assembly from Illumina sequencing reads. A total of 92,498 (66.38%) unigenes showed similarities in at least one database including Nr (46.15%), Nt (56.56%), KO (15.56%), Swiss-prot (33.34%), Pfam (33.43%), GO (33.62%) and KOG/COG (17.55%). Genes in flavonoid and taurine biosynthesis pathways were found and validated by RT-qPCR. A total of 50,093 EST-SSRs were identified from 38,922 unigenes, and 22,537 EST-SSR primer pairs were designed. Four hundred pairs of SSR markers were randomly selected to validate assembly quality, of which 352 (88%) were successful in PCR amplification of genomic DNA from 11 Lycium accessions and 210 produced polymorphisms. The polymorphic loci showed that the genetic similarity of the 11 Lycium accessions ranged from 0.50 to 0.99 and the accessions could be divided into 4 groups. These results will facilitate investigations of the molecular mechanism of formation of L. barbarum fruit and associated medicinal and nutritional components, and will be of value to novel gene discovery and functional genomic studies. The EST-SSR markers will be useful for genetic diversity evaluation, genetic mapping and marker-assisted breeding.
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spelling pubmed-56952792017-11-30 Characterization of the Lycium barbarum fruit transcriptome and development of EST-SSR markers Chen, Chunling Xu, Meilong Wang, Cuiping Qiao, Gaixia Wang, Wenwen Tan, Zhaoyun Wu, Tiantian Zhang, Zhengsheng PLoS One Research Article Lycium barbarum, commonly known as goji, is important in Chinese herbal medicine and its fruit is a very important agricultural and biological product. However, the molecular mechanism of formation of its fruit and associated medicinal and nutritional components is unexplored. Moreover, this species lacks SSR markers due to lack of genomic and transcriptomic information. In this study, a total of 139,333 unigenes with average length of 1049 bp and N50 of 1579 bp are obtained by trinity assembly from Illumina sequencing reads. A total of 92,498 (66.38%) unigenes showed similarities in at least one database including Nr (46.15%), Nt (56.56%), KO (15.56%), Swiss-prot (33.34%), Pfam (33.43%), GO (33.62%) and KOG/COG (17.55%). Genes in flavonoid and taurine biosynthesis pathways were found and validated by RT-qPCR. A total of 50,093 EST-SSRs were identified from 38,922 unigenes, and 22,537 EST-SSR primer pairs were designed. Four hundred pairs of SSR markers were randomly selected to validate assembly quality, of which 352 (88%) were successful in PCR amplification of genomic DNA from 11 Lycium accessions and 210 produced polymorphisms. The polymorphic loci showed that the genetic similarity of the 11 Lycium accessions ranged from 0.50 to 0.99 and the accessions could be divided into 4 groups. These results will facilitate investigations of the molecular mechanism of formation of L. barbarum fruit and associated medicinal and nutritional components, and will be of value to novel gene discovery and functional genomic studies. The EST-SSR markers will be useful for genetic diversity evaluation, genetic mapping and marker-assisted breeding. Public Library of Science 2017-11-10 /pmc/articles/PMC5695279/ /pubmed/29125846 http://dx.doi.org/10.1371/journal.pone.0187738 Text en © 2017 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, Chunling
Xu, Meilong
Wang, Cuiping
Qiao, Gaixia
Wang, Wenwen
Tan, Zhaoyun
Wu, Tiantian
Zhang, Zhengsheng
Characterization of the Lycium barbarum fruit transcriptome and development of EST-SSR markers
title Characterization of the Lycium barbarum fruit transcriptome and development of EST-SSR markers
title_full Characterization of the Lycium barbarum fruit transcriptome and development of EST-SSR markers
title_fullStr Characterization of the Lycium barbarum fruit transcriptome and development of EST-SSR markers
title_full_unstemmed Characterization of the Lycium barbarum fruit transcriptome and development of EST-SSR markers
title_short Characterization of the Lycium barbarum fruit transcriptome and development of EST-SSR markers
title_sort characterization of the lycium barbarum fruit transcriptome and development of est-ssr markers
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5695279/
https://www.ncbi.nlm.nih.gov/pubmed/29125846
http://dx.doi.org/10.1371/journal.pone.0187738
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