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Development and Characterization of Microsatellite Markers Based on the Chloroplast Genome of Tree Peony

Tree peony (Paeonia suffruticosa Andr.) is a famous ornamental and medicinal flowering species. However, few high-efficiency chloroplast microsatellite markers have been developed for it to be employed in taxonomic identifications and evaluation of germplasm resources to date. In the present study,...

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Autores principales: Guo, Qi, Guo, Lili, Li, Yuying, Yang, Haijing, Hu, Xiaoliang, Song, Chengwei, Hou, Xiaogai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9498374/
https://www.ncbi.nlm.nih.gov/pubmed/36140711
http://dx.doi.org/10.3390/genes13091543
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author Guo, Qi
Guo, Lili
Li, Yuying
Yang, Haijing
Hu, Xiaoliang
Song, Chengwei
Hou, Xiaogai
author_facet Guo, Qi
Guo, Lili
Li, Yuying
Yang, Haijing
Hu, Xiaoliang
Song, Chengwei
Hou, Xiaogai
author_sort Guo, Qi
collection PubMed
description Tree peony (Paeonia suffruticosa Andr.) is a famous ornamental and medicinal flowering species. However, few high-efficiency chloroplast microsatellite markers have been developed for it to be employed in taxonomic identifications and evaluation of germplasm resources to date. In the present study, a total of 139 cpSSR loci were identified across eleven tree peony plastomes. Dinucleotide repeat SSRs (97.12%) were most abundantly repeated for the AT motif (58.27%), followed by the TA motif (30.94%) and the TC motif (7.91%). Twenty-one primer pairs were developed, and amplification tests were conducted for nine tree peony individuals. Furthermore, 19 cpSSR markers were amplified on 60 tree peony accessions by a capillary electrophoresis test. Of 19 cpSSR markers, 12 showed polymorphism with different alleles ranging from 1.333 to 3.000. The Shannon’s information index and polymorphism information content values ranged from 0.038 to 0.887 (mean 0.432) and 0.032 to 0.589 (mean 0.268), respectively. The diversity levels for twelve loci ranged from 0.016 (at loci cpSSR-8 and cpSSR-26) to 0.543 (at locus cpSSR-15), averaging 0.268 for all loci. A total of 14 haplotypes (23.33%) were detected in the three populations. The haplotypic richness ranged from 0.949 to 1.751, with a mean of 1.233 per population. The genetic relationship suggested by the neighbor-joining-based dendrogram divided the genotypes into two clusters. The Jiangnan population was allotted to Cluster II, and the other two populations were distributed into both branches. These newly developed cpSSRs can be utilized for future breeding programs, population genetics investigations, unraveling the genetic relationships between related species, and germplasm management.
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spelling pubmed-94983742022-09-23 Development and Characterization of Microsatellite Markers Based on the Chloroplast Genome of Tree Peony Guo, Qi Guo, Lili Li, Yuying Yang, Haijing Hu, Xiaoliang Song, Chengwei Hou, Xiaogai Genes (Basel) Communication Tree peony (Paeonia suffruticosa Andr.) is a famous ornamental and medicinal flowering species. However, few high-efficiency chloroplast microsatellite markers have been developed for it to be employed in taxonomic identifications and evaluation of germplasm resources to date. In the present study, a total of 139 cpSSR loci were identified across eleven tree peony plastomes. Dinucleotide repeat SSRs (97.12%) were most abundantly repeated for the AT motif (58.27%), followed by the TA motif (30.94%) and the TC motif (7.91%). Twenty-one primer pairs were developed, and amplification tests were conducted for nine tree peony individuals. Furthermore, 19 cpSSR markers were amplified on 60 tree peony accessions by a capillary electrophoresis test. Of 19 cpSSR markers, 12 showed polymorphism with different alleles ranging from 1.333 to 3.000. The Shannon’s information index and polymorphism information content values ranged from 0.038 to 0.887 (mean 0.432) and 0.032 to 0.589 (mean 0.268), respectively. The diversity levels for twelve loci ranged from 0.016 (at loci cpSSR-8 and cpSSR-26) to 0.543 (at locus cpSSR-15), averaging 0.268 for all loci. A total of 14 haplotypes (23.33%) were detected in the three populations. The haplotypic richness ranged from 0.949 to 1.751, with a mean of 1.233 per population. The genetic relationship suggested by the neighbor-joining-based dendrogram divided the genotypes into two clusters. The Jiangnan population was allotted to Cluster II, and the other two populations were distributed into both branches. These newly developed cpSSRs can be utilized for future breeding programs, population genetics investigations, unraveling the genetic relationships between related species, and germplasm management. MDPI 2022-08-26 /pmc/articles/PMC9498374/ /pubmed/36140711 http://dx.doi.org/10.3390/genes13091543 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Communication
Guo, Qi
Guo, Lili
Li, Yuying
Yang, Haijing
Hu, Xiaoliang
Song, Chengwei
Hou, Xiaogai
Development and Characterization of Microsatellite Markers Based on the Chloroplast Genome of Tree Peony
title Development and Characterization of Microsatellite Markers Based on the Chloroplast Genome of Tree Peony
title_full Development and Characterization of Microsatellite Markers Based on the Chloroplast Genome of Tree Peony
title_fullStr Development and Characterization of Microsatellite Markers Based on the Chloroplast Genome of Tree Peony
title_full_unstemmed Development and Characterization of Microsatellite Markers Based on the Chloroplast Genome of Tree Peony
title_short Development and Characterization of Microsatellite Markers Based on the Chloroplast Genome of Tree Peony
title_sort development and characterization of microsatellite markers based on the chloroplast genome of tree peony
topic Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9498374/
https://www.ncbi.nlm.nih.gov/pubmed/36140711
http://dx.doi.org/10.3390/genes13091543
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