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Chimeras in Merlot grapevine revealed by phased assembly

Chimerism is the phenomenon when several genotypes coexist in a single individual. Used to understand plant ontogenesis they also have been valorised through new cultivar breeding. Viticulture has been taking economic advantage out of chimeras when the variant induced an important modification of wi...

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Autores principales: Sichel, V., Sarah, G., Girollet, N., Laucou, V., Roux, C., Roques, M., Mournet, P., Cunff, L. Le, Bert, P.F., This, P., Lacombe, T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10347889/
https://www.ncbi.nlm.nih.gov/pubmed/37452318
http://dx.doi.org/10.1186/s12864-023-09453-8
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author Sichel, V.
Sarah, G.
Girollet, N.
Laucou, V.
Roux, C.
Roques, M.
Mournet, P.
Cunff, L. Le
Bert, P.F.
This, P.
Lacombe, T.
author_facet Sichel, V.
Sarah, G.
Girollet, N.
Laucou, V.
Roux, C.
Roques, M.
Mournet, P.
Cunff, L. Le
Bert, P.F.
This, P.
Lacombe, T.
author_sort Sichel, V.
collection PubMed
description Chimerism is the phenomenon when several genotypes coexist in a single individual. Used to understand plant ontogenesis they also have been valorised through new cultivar breeding. Viticulture has been taking economic advantage out of chimeras when the variant induced an important modification of wine type such as berry skin colour. Crucial agronomic characters may also be impacted by chimeras that aren’t identified yet. Periclinal chimera where the variant has entirely colonised a cell layer is the most stable and can be propagated through cuttings. In grapevine, leaves are derived from both meristem layers, L1 and L2. However, lateral roots are formed from the L2 cell layer only. Thus, comparing DNA sequences of roots and leaves allows chimera detection. In this study we used new generation Hifi long reads sequencing, recent bioinformatics tools and trio-binning with parental sequences to detect periclinal chimeras on ‘Merlot’ grapevine cultivar. Sequencing of cv. ‘Magdeleine Noire des Charentes’ and ‘Cabernet Franc’, the parents of cv. ‘Merlot’, allowed haplotype resolved assembly. Pseudomolecules were built with a total of 33 to 47 contigs and in few occasions a unique contig for one chromosome. This high resolution allowed haplotype comparison. Annotation was transferred from PN40024 VCost.v3 to all pseudomolecules. After strong selection of variants, 51 and 53 ‘Merlot’ specific periclinal chimeras were found on the Merlot-haplotype-CF and Merlot-haplotype-MG respectively, 9 and 7 been located in a coding region. A subset of positions was analysed using Molecular Inversion Probes (MIPseq) and 69% were unambiguously validated, 25% are doubtful because of technological noise or weak depth and 6% invalidated. These results open new perspectives on chimera detection as an important resource to improve cultivars through clonal selection or breeding. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-023-09453-8.
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spelling pubmed-103478892023-07-15 Chimeras in Merlot grapevine revealed by phased assembly Sichel, V. Sarah, G. Girollet, N. Laucou, V. Roux, C. Roques, M. Mournet, P. Cunff, L. Le Bert, P.F. This, P. Lacombe, T. BMC Genomics Research Article Chimerism is the phenomenon when several genotypes coexist in a single individual. Used to understand plant ontogenesis they also have been valorised through new cultivar breeding. Viticulture has been taking economic advantage out of chimeras when the variant induced an important modification of wine type such as berry skin colour. Crucial agronomic characters may also be impacted by chimeras that aren’t identified yet. Periclinal chimera where the variant has entirely colonised a cell layer is the most stable and can be propagated through cuttings. In grapevine, leaves are derived from both meristem layers, L1 and L2. However, lateral roots are formed from the L2 cell layer only. Thus, comparing DNA sequences of roots and leaves allows chimera detection. In this study we used new generation Hifi long reads sequencing, recent bioinformatics tools and trio-binning with parental sequences to detect periclinal chimeras on ‘Merlot’ grapevine cultivar. Sequencing of cv. ‘Magdeleine Noire des Charentes’ and ‘Cabernet Franc’, the parents of cv. ‘Merlot’, allowed haplotype resolved assembly. Pseudomolecules were built with a total of 33 to 47 contigs and in few occasions a unique contig for one chromosome. This high resolution allowed haplotype comparison. Annotation was transferred from PN40024 VCost.v3 to all pseudomolecules. After strong selection of variants, 51 and 53 ‘Merlot’ specific periclinal chimeras were found on the Merlot-haplotype-CF and Merlot-haplotype-MG respectively, 9 and 7 been located in a coding region. A subset of positions was analysed using Molecular Inversion Probes (MIPseq) and 69% were unambiguously validated, 25% are doubtful because of technological noise or weak depth and 6% invalidated. These results open new perspectives on chimera detection as an important resource to improve cultivars through clonal selection or breeding. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-023-09453-8. BioMed Central 2023-07-14 /pmc/articles/PMC10347889/ /pubmed/37452318 http://dx.doi.org/10.1186/s12864-023-09453-8 Text en © The Author(s) 2023 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Sichel, V.
Sarah, G.
Girollet, N.
Laucou, V.
Roux, C.
Roques, M.
Mournet, P.
Cunff, L. Le
Bert, P.F.
This, P.
Lacombe, T.
Chimeras in Merlot grapevine revealed by phased assembly
title Chimeras in Merlot grapevine revealed by phased assembly
title_full Chimeras in Merlot grapevine revealed by phased assembly
title_fullStr Chimeras in Merlot grapevine revealed by phased assembly
title_full_unstemmed Chimeras in Merlot grapevine revealed by phased assembly
title_short Chimeras in Merlot grapevine revealed by phased assembly
title_sort chimeras in merlot grapevine revealed by phased assembly
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10347889/
https://www.ncbi.nlm.nih.gov/pubmed/37452318
http://dx.doi.org/10.1186/s12864-023-09453-8
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