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High variability in SSU rDNA gene copy number among planktonic foraminifera revealed by single-cell qPCR

Metabarcoding has become the workhorse of community ecology. Sequencing a taxonomically informative DNA fragment from environmental samples gives fast access to community composition across taxonomic groups, but it relies on the assumption that the number of sequences for each taxon correlates with...

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Autores principales: Milivojević, Tamara, Rahman, Shirin Nurshan, Raposo, Débora, Siccha, Michael, Kucera, Michal, Morard, Raphaël
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9723665/
https://www.ncbi.nlm.nih.gov/pubmed/36750661
http://dx.doi.org/10.1038/s43705-021-00067-3
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author Milivojević, Tamara
Rahman, Shirin Nurshan
Raposo, Débora
Siccha, Michael
Kucera, Michal
Morard, Raphaël
author_facet Milivojević, Tamara
Rahman, Shirin Nurshan
Raposo, Débora
Siccha, Michael
Kucera, Michal
Morard, Raphaël
author_sort Milivojević, Tamara
collection PubMed
description Metabarcoding has become the workhorse of community ecology. Sequencing a taxonomically informative DNA fragment from environmental samples gives fast access to community composition across taxonomic groups, but it relies on the assumption that the number of sequences for each taxon correlates with its abundance in the sampled community. However, gene copy number varies among and within taxa, and the extent of this variability must therefore be considered when interpreting community composition data derived from environmental sequencing. Here we measured with single-cell qPCR the SSU rDNA gene copy number of 139 specimens of five species of planktonic foraminifera. We found that the average gene copy number varied between of ~4000 to ~50,000 gene copies between species, and individuals of the same species can carry between ~300 to more than 350,000 gene copies. This variability cannot be explained by differences in cell size and considering all plausible sources of bias, we conclude that this variability likely reflects dynamic genomic processes acting during the life cycle. We used the observed variability to model its impact on metabarcoding and found that the application of a correcting factor at species level may correct the derived relative abundances, provided sufficiently large populations have been sampled.
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spelling pubmed-97236652023-01-04 High variability in SSU rDNA gene copy number among planktonic foraminifera revealed by single-cell qPCR Milivojević, Tamara Rahman, Shirin Nurshan Raposo, Débora Siccha, Michael Kucera, Michal Morard, Raphaël ISME Commun Article Metabarcoding has become the workhorse of community ecology. Sequencing a taxonomically informative DNA fragment from environmental samples gives fast access to community composition across taxonomic groups, but it relies on the assumption that the number of sequences for each taxon correlates with its abundance in the sampled community. However, gene copy number varies among and within taxa, and the extent of this variability must therefore be considered when interpreting community composition data derived from environmental sequencing. Here we measured with single-cell qPCR the SSU rDNA gene copy number of 139 specimens of five species of planktonic foraminifera. We found that the average gene copy number varied between of ~4000 to ~50,000 gene copies between species, and individuals of the same species can carry between ~300 to more than 350,000 gene copies. This variability cannot be explained by differences in cell size and considering all plausible sources of bias, we conclude that this variability likely reflects dynamic genomic processes acting during the life cycle. We used the observed variability to model its impact on metabarcoding and found that the application of a correcting factor at species level may correct the derived relative abundances, provided sufficiently large populations have been sampled. Nature Publishing Group UK 2021-10-30 /pmc/articles/PMC9723665/ /pubmed/36750661 http://dx.doi.org/10.1038/s43705-021-00067-3 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Milivojević, Tamara
Rahman, Shirin Nurshan
Raposo, Débora
Siccha, Michael
Kucera, Michal
Morard, Raphaël
High variability in SSU rDNA gene copy number among planktonic foraminifera revealed by single-cell qPCR
title High variability in SSU rDNA gene copy number among planktonic foraminifera revealed by single-cell qPCR
title_full High variability in SSU rDNA gene copy number among planktonic foraminifera revealed by single-cell qPCR
title_fullStr High variability in SSU rDNA gene copy number among planktonic foraminifera revealed by single-cell qPCR
title_full_unstemmed High variability in SSU rDNA gene copy number among planktonic foraminifera revealed by single-cell qPCR
title_short High variability in SSU rDNA gene copy number among planktonic foraminifera revealed by single-cell qPCR
title_sort high variability in ssu rdna gene copy number among planktonic foraminifera revealed by single-cell qpcr
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9723665/
https://www.ncbi.nlm.nih.gov/pubmed/36750661
http://dx.doi.org/10.1038/s43705-021-00067-3
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