Intra‐individual polymorphism in chloroplasts from NGS data: where does it come from and how to handle it?

Next‐generation sequencing allows access to a large quantity of genomic data. In plants, several studies used whole chloroplast genome sequences for inferring phylogeography or phylogeny. Even though the chloroplast is a haploid organelle, NGS plastome data identified a nonnegligible number of intra...

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Published inMolecular ecology resources Vol. 16; no. 2; pp. 434 - 445
Main Authors Scarcelli, N., Mariac, C., Couvreur, T. L. P., Faye, A., Richard, D., Sabot, F., Berthouly-Salazar, C., Vigouroux, Y.
Format Journal Article
LanguageEnglish
Published England Blackwell Pub 01.03.2016
Blackwell Publishing Ltd
Wiley Subscription Services, Inc
Wiley/Blackwell
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Summary:Next‐generation sequencing allows access to a large quantity of genomic data. In plants, several studies used whole chloroplast genome sequences for inferring phylogeography or phylogeny. Even though the chloroplast is a haploid organelle, NGS plastome data identified a nonnegligible number of intra‐individual polymorphic SNPs. Such observations could have several causes such as sequencing errors, the presence of heteroplasmy or transfer of chloroplast sequences in the nuclear and mitochondrial genomes. The occurrence of allelic diversity has practical important impacts on the identification of diversity, the analysis of the chloroplast data and beyond that, significant evolutionary questions. In this study, we show that the observed intra‐individual polymorphism of chloroplast sequence data is probably the result of plastid DNA transferred into the mitochondrial and/or the nuclear genomes. We further assess nine different bioinformatics pipelines’ error rates for SNP and genotypes calling using SNPs identified in Sanger sequencing. Specific pipelines are adequate to deal with this issue, optimizing both specificity and sensitivity. Our results will allow a proper use of whole chloroplast NGS sequence and will allow a better handling of NGS chloroplast sequence diversity.
Bibliography:http://dx.doi.org/10.1111/1755-0998.12462
Agropolis Foundation - No. ANR-10-LABX-0001-01
ark:/67375/WNG-6LN1K7PD-L
istex:FEAB7BB6E6A1D8A7555A7E69B4A58C3C57090B89
Agence Nationale de Recherche - No. AFRICROP ANR-13-BSV7-0017
Table S1 List of GenBank (.fasta), NCBI-SRA (.fastq) and DRYAD (.fastq, .bam and .vcf) ID resources used in this paper.Table S2 Scripts used to prepare raw data, map to the reference and call SNPs (12 different methods). List of adaptors and tags used during the libraries' construction.Table S3 Number of reads mapping on the chloroplast, mitochondrial and nuclear genomes for the rice sample.Table S4 Total number of SNP [1,1] and polymorphic positions [0,1] observed for each species and for each calling method.
ArticleID:MEN12462
ObjectType-Article-1
SourceType-Scholarly Journals-1
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ISSN:1755-098X
1755-0998
DOI:10.1111/1755-0998.12462