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Development of microsatellite markers and assembly of the plastid genome in Cistanthe longiscapa (Montiaceae) based on low-coverage whole genome sequencing

Cistanthe longiscapa is an endemic annual herb and characteristic element of the Chilean Atacama Desert. Principal threats are the destruction of its seed deposits by human activities and reduced germination rates due to the decreasing occurrence of precipitation events. To enable population genetic...

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Autores principales: Stoll, Alexandra, Harpke, Dörte, Schütte, Claudia, Stefanczyk, Nadine, Brandt, Ronny, Blattner, Frank R., Quandt, Dietmar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5456083/
https://www.ncbi.nlm.nih.gov/pubmed/28575007
http://dx.doi.org/10.1371/journal.pone.0178402
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author Stoll, Alexandra
Harpke, Dörte
Schütte, Claudia
Stefanczyk, Nadine
Brandt, Ronny
Blattner, Frank R.
Quandt, Dietmar
author_facet Stoll, Alexandra
Harpke, Dörte
Schütte, Claudia
Stefanczyk, Nadine
Brandt, Ronny
Blattner, Frank R.
Quandt, Dietmar
author_sort Stoll, Alexandra
collection PubMed
description Cistanthe longiscapa is an endemic annual herb and characteristic element of the Chilean Atacama Desert. Principal threats are the destruction of its seed deposits by human activities and reduced germination rates due to the decreasing occurrence of precipitation events. To enable population genetic and phylogeographic analyses in this species we performed paired-end shotgun sequencing (2x100 bp) of genomic DNA on the Illumina HiSeq platform and identified microsatellite (SSR) loci in the resulting sequences. From 29 million quality-filtered read pairs we obtained 549,174 contigs (average length 614 bp; N50 = 904). Searching for SSRs revealed 10,336 loci with microsatellite motifs. Initially, we designed primers for 96 loci, which were tested for PCR amplification on three C. longiscapa individuals. Successfully amplifying loci were further tested on eight individuals to screen for length variation in the resulting amplicons, and the alleles were exemplarily sequenced to infer the basis for the observed length variation. Finally we arrived at 26 validated SSR loci for population studies in C. longiscapa, which resulted in 146 bi-allelic SSR markers in our test sample of eight individuals. The genomic sequences were also used to assemble the plastid genome of C. longiscapa, which provides an additional set of maternally inherited genetic markers.
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spelling pubmed-54560832017-06-12 Development of microsatellite markers and assembly of the plastid genome in Cistanthe longiscapa (Montiaceae) based on low-coverage whole genome sequencing Stoll, Alexandra Harpke, Dörte Schütte, Claudia Stefanczyk, Nadine Brandt, Ronny Blattner, Frank R. Quandt, Dietmar PLoS One Research Article Cistanthe longiscapa is an endemic annual herb and characteristic element of the Chilean Atacama Desert. Principal threats are the destruction of its seed deposits by human activities and reduced germination rates due to the decreasing occurrence of precipitation events. To enable population genetic and phylogeographic analyses in this species we performed paired-end shotgun sequencing (2x100 bp) of genomic DNA on the Illumina HiSeq platform and identified microsatellite (SSR) loci in the resulting sequences. From 29 million quality-filtered read pairs we obtained 549,174 contigs (average length 614 bp; N50 = 904). Searching for SSRs revealed 10,336 loci with microsatellite motifs. Initially, we designed primers for 96 loci, which were tested for PCR amplification on three C. longiscapa individuals. Successfully amplifying loci were further tested on eight individuals to screen for length variation in the resulting amplicons, and the alleles were exemplarily sequenced to infer the basis for the observed length variation. Finally we arrived at 26 validated SSR loci for population studies in C. longiscapa, which resulted in 146 bi-allelic SSR markers in our test sample of eight individuals. The genomic sequences were also used to assemble the plastid genome of C. longiscapa, which provides an additional set of maternally inherited genetic markers. Public Library of Science 2017-06-02 /pmc/articles/PMC5456083/ /pubmed/28575007 http://dx.doi.org/10.1371/journal.pone.0178402 Text en © 2017 Stoll 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
Stoll, Alexandra
Harpke, Dörte
Schütte, Claudia
Stefanczyk, Nadine
Brandt, Ronny
Blattner, Frank R.
Quandt, Dietmar
Development of microsatellite markers and assembly of the plastid genome in Cistanthe longiscapa (Montiaceae) based on low-coverage whole genome sequencing
title Development of microsatellite markers and assembly of the plastid genome in Cistanthe longiscapa (Montiaceae) based on low-coverage whole genome sequencing
title_full Development of microsatellite markers and assembly of the plastid genome in Cistanthe longiscapa (Montiaceae) based on low-coverage whole genome sequencing
title_fullStr Development of microsatellite markers and assembly of the plastid genome in Cistanthe longiscapa (Montiaceae) based on low-coverage whole genome sequencing
title_full_unstemmed Development of microsatellite markers and assembly of the plastid genome in Cistanthe longiscapa (Montiaceae) based on low-coverage whole genome sequencing
title_short Development of microsatellite markers and assembly of the plastid genome in Cistanthe longiscapa (Montiaceae) based on low-coverage whole genome sequencing
title_sort development of microsatellite markers and assembly of the plastid genome in cistanthe longiscapa (montiaceae) based on low-coverage whole genome sequencing
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5456083/
https://www.ncbi.nlm.nih.gov/pubmed/28575007
http://dx.doi.org/10.1371/journal.pone.0178402
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