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Development and Application of EST-SSR Markers in Cephalotaxus oliveri From Transcriptome Sequences
Cephalotaxus oliveri is an endemic conifer of China, which has medicinal and ornamental value. However, the limited molecular markers and genetic information are insufficient for further genetic studies of this species. In this study, we characterized and developed the EST-SSRs from transcriptome se...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8635753/ https://www.ncbi.nlm.nih.gov/pubmed/34868238 http://dx.doi.org/10.3389/fgene.2021.759557 |
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author | Liu, Hanjing Zhang, Yuli Wang, Zhen Su, Yingjuan Wang, Ting |
author_facet | Liu, Hanjing Zhang, Yuli Wang, Zhen Su, Yingjuan Wang, Ting |
author_sort | Liu, Hanjing |
collection | PubMed |
description | Cephalotaxus oliveri is an endemic conifer of China, which has medicinal and ornamental value. However, the limited molecular markers and genetic information are insufficient for further genetic studies of this species. In this study, we characterized and developed the EST-SSRs from transcriptome sequences for the first time. The results showed that a total of 5089 SSRs were identified from 36446 unigenes with a density of one SSR per 11.1 kb. The most common type was trinucleotide repeats, excluding mononucleotide repeats, followed by dinucleotide repeats. AAG/CTT and AT/AT exhibited the highest frequency in the trinucleotide and dinucleotide repeats, respectively. Of the identified SSRs, 671, 1125, and 1958 SSRs were located in CDS, 3′UTR, and 5′UTR, respectively. Functional annotation showed that the SSR-containing unigenes were involved in growth and development with various biological functions. Among successfully designed primer pairs, 238 primer pairs were randomly selected for amplification and validation of EST-SSR markers and 47 primer pairs were identified as polymorphic. Finally, 28 high-polymorphic primers were used for genetic analysis and revealed a moderate level of genetic diversity. Seven natural C. oliveri sampling sites were divided into two genetic groups. Furthermore, the 28 EST-SSRs had 96.43, 71.43, and 78.57% of transferability rate in Cephalotaxus fortune, Ametotaxus argotaenia, and Pseudotaxus chienii, respectively. These markers developed in this study lay the foundation for further genetic and adaptive evolution studies in C. oliveri and related species. |
format | Online Article Text |
id | pubmed-8635753 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-86357532021-12-02 Development and Application of EST-SSR Markers in Cephalotaxus oliveri From Transcriptome Sequences Liu, Hanjing Zhang, Yuli Wang, Zhen Su, Yingjuan Wang, Ting Front Genet Genetics Cephalotaxus oliveri is an endemic conifer of China, which has medicinal and ornamental value. However, the limited molecular markers and genetic information are insufficient for further genetic studies of this species. In this study, we characterized and developed the EST-SSRs from transcriptome sequences for the first time. The results showed that a total of 5089 SSRs were identified from 36446 unigenes with a density of one SSR per 11.1 kb. The most common type was trinucleotide repeats, excluding mononucleotide repeats, followed by dinucleotide repeats. AAG/CTT and AT/AT exhibited the highest frequency in the trinucleotide and dinucleotide repeats, respectively. Of the identified SSRs, 671, 1125, and 1958 SSRs were located in CDS, 3′UTR, and 5′UTR, respectively. Functional annotation showed that the SSR-containing unigenes were involved in growth and development with various biological functions. Among successfully designed primer pairs, 238 primer pairs were randomly selected for amplification and validation of EST-SSR markers and 47 primer pairs were identified as polymorphic. Finally, 28 high-polymorphic primers were used for genetic analysis and revealed a moderate level of genetic diversity. Seven natural C. oliveri sampling sites were divided into two genetic groups. Furthermore, the 28 EST-SSRs had 96.43, 71.43, and 78.57% of transferability rate in Cephalotaxus fortune, Ametotaxus argotaenia, and Pseudotaxus chienii, respectively. These markers developed in this study lay the foundation for further genetic and adaptive evolution studies in C. oliveri and related species. Frontiers Media S.A. 2021-11-17 /pmc/articles/PMC8635753/ /pubmed/34868238 http://dx.doi.org/10.3389/fgene.2021.759557 Text en Copyright © 2021 Liu, Zhang, Wang, Su and Wang. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Genetics Liu, Hanjing Zhang, Yuli Wang, Zhen Su, Yingjuan Wang, Ting Development and Application of EST-SSR Markers in Cephalotaxus oliveri From Transcriptome Sequences |
title | Development and Application of EST-SSR Markers in Cephalotaxus oliveri From Transcriptome Sequences |
title_full | Development and Application of EST-SSR Markers in Cephalotaxus oliveri From Transcriptome Sequences |
title_fullStr | Development and Application of EST-SSR Markers in Cephalotaxus oliveri From Transcriptome Sequences |
title_full_unstemmed | Development and Application of EST-SSR Markers in Cephalotaxus oliveri From Transcriptome Sequences |
title_short | Development and Application of EST-SSR Markers in Cephalotaxus oliveri From Transcriptome Sequences |
title_sort | development and application of est-ssr markers in cephalotaxus oliveri from transcriptome sequences |
topic | Genetics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8635753/ https://www.ncbi.nlm.nih.gov/pubmed/34868238 http://dx.doi.org/10.3389/fgene.2021.759557 |
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