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SAG-RAD: A Method for Single-Cell Population Genomics of Unicellular Eukaryotes

Sequencing of reduced representation libraries enables genotyping of many individuals for population genomic studies. However, high amounts of DNA are required, and the method cannot be applied directly on single cells, preventing its use on most microbes. We developed and implemented the analysis o...

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Detalles Bibliográficos
Autores principales: Gollnisch, Raphael, Wallenius, Joel, Gribble, Kristin E, Ahrén, Dag, Rengefors, Karin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10202595/
https://www.ncbi.nlm.nih.gov/pubmed/37079883
http://dx.doi.org/10.1093/molbev/msad095
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author Gollnisch, Raphael
Wallenius, Joel
Gribble, Kristin E
Ahrén, Dag
Rengefors, Karin
author_facet Gollnisch, Raphael
Wallenius, Joel
Gribble, Kristin E
Ahrén, Dag
Rengefors, Karin
author_sort Gollnisch, Raphael
collection PubMed
description Sequencing of reduced representation libraries enables genotyping of many individuals for population genomic studies. However, high amounts of DNA are required, and the method cannot be applied directly on single cells, preventing its use on most microbes. We developed and implemented the analysis of single amplified genomes followed by restriction-site-associated DNA sequencing to bypass labor-intensive culturing and to avoid culturing bias in population genomic studies of unicellular eukaryotes. This method thus opens the way for addressing important questions about the genetic diversity, gene flow, adaptation, dispersal, and biogeography of hitherto unexplored species.
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spelling pubmed-102025952023-05-23 SAG-RAD: A Method for Single-Cell Population Genomics of Unicellular Eukaryotes Gollnisch, Raphael Wallenius, Joel Gribble, Kristin E Ahrén, Dag Rengefors, Karin Mol Biol Evol Methods Sequencing of reduced representation libraries enables genotyping of many individuals for population genomic studies. However, high amounts of DNA are required, and the method cannot be applied directly on single cells, preventing its use on most microbes. We developed and implemented the analysis of single amplified genomes followed by restriction-site-associated DNA sequencing to bypass labor-intensive culturing and to avoid culturing bias in population genomic studies of unicellular eukaryotes. This method thus opens the way for addressing important questions about the genetic diversity, gene flow, adaptation, dispersal, and biogeography of hitherto unexplored species. Oxford University Press 2023-04-20 /pmc/articles/PMC10202595/ /pubmed/37079883 http://dx.doi.org/10.1093/molbev/msad095 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of Society for Molecular Biology and Evolution. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Methods
Gollnisch, Raphael
Wallenius, Joel
Gribble, Kristin E
Ahrén, Dag
Rengefors, Karin
SAG-RAD: A Method for Single-Cell Population Genomics of Unicellular Eukaryotes
title SAG-RAD: A Method for Single-Cell Population Genomics of Unicellular Eukaryotes
title_full SAG-RAD: A Method for Single-Cell Population Genomics of Unicellular Eukaryotes
title_fullStr SAG-RAD: A Method for Single-Cell Population Genomics of Unicellular Eukaryotes
title_full_unstemmed SAG-RAD: A Method for Single-Cell Population Genomics of Unicellular Eukaryotes
title_short SAG-RAD: A Method for Single-Cell Population Genomics of Unicellular Eukaryotes
title_sort sag-rad: a method for single-cell population genomics of unicellular eukaryotes
topic Methods
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10202595/
https://www.ncbi.nlm.nih.gov/pubmed/37079883
http://dx.doi.org/10.1093/molbev/msad095
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