'Nebbiolo' genome assembly allows surveying the occurrence and functional implications of genomic structural variations in grapevines (Vitis vinifera L.).


Journal

BMC genomics
ISSN: 1471-2164
Titre abrégé: BMC Genomics
Pays: England
ID NLM: 100965258

Informations de publication

Date de publication:
24 Feb 2022
Historique:
received: 08 09 2021
accepted: 15 02 2022
entrez: 25 2 2022
pubmed: 26 2 2022
medline: 1 3 2022
Statut: epublish

Résumé

'Nebbiolo' is a grapevine cultivar typical of north-western Italy, appreciated for producing high-quality red wines. Grapevine cultivars are characterized by possessing highly heterozygous genomes, including a great incidence of genomic rearrangements larger than 50 bp, so called structural variations (SVs). Even though abundant, SVs are an under-explored source of genetic variation mainly due to methodological limitations at their detection. We employed a multiple platform approach to produce long-range genomic data for two different 'Nebbiolo' clones, namely: optical mapping, long-reads and linked-reads. We performed a haplotype-resolved de novo assembly for cultivar 'Nebbiolo' (clone CVT 71) and used an ab-initio strategy to annotate it. The annotated assembly enhanced our ability to detect SVs, enabling the study of genomic regions not present in the grapevines' reference genome and accounting for their functional implications. We performed variant calling analyses at three different organizational levels: i) between haplotypes of clone CVT 71 (primary assembly vs haplotigs), ii) between 'Nebbiolo' and 'Cabernet Sauvignon' assemblies and iii) between clones CVT 71 and CVT 185, representing different 'Nebbiolo' biotypes. The cumulative size of non-redundant merged SVs indicated a total of 79.6 Mbp for the first comparison and 136.1 Mbp for the second one, while no SVs were detected for the third comparison. Interestingly, SVs differentiating cultivars and haplotypes affected similar numbers of coding genes. Our results suggest that SVs accumulation rate and their functional implications in 'Nebbiolo' genome are highly-dependent on the organizational level under study. SVs are abundant when comparing 'Nebbiolo' to a different cultivar or the two haplotypes of the same individual, while they turned absent between the two analysed clones.

Sections du résumé

BACKGROUND BACKGROUND
'Nebbiolo' is a grapevine cultivar typical of north-western Italy, appreciated for producing high-quality red wines. Grapevine cultivars are characterized by possessing highly heterozygous genomes, including a great incidence of genomic rearrangements larger than 50 bp, so called structural variations (SVs). Even though abundant, SVs are an under-explored source of genetic variation mainly due to methodological limitations at their detection.
RESULTS RESULTS
We employed a multiple platform approach to produce long-range genomic data for two different 'Nebbiolo' clones, namely: optical mapping, long-reads and linked-reads. We performed a haplotype-resolved de novo assembly for cultivar 'Nebbiolo' (clone CVT 71) and used an ab-initio strategy to annotate it. The annotated assembly enhanced our ability to detect SVs, enabling the study of genomic regions not present in the grapevines' reference genome and accounting for their functional implications. We performed variant calling analyses at three different organizational levels: i) between haplotypes of clone CVT 71 (primary assembly vs haplotigs), ii) between 'Nebbiolo' and 'Cabernet Sauvignon' assemblies and iii) between clones CVT 71 and CVT 185, representing different 'Nebbiolo' biotypes. The cumulative size of non-redundant merged SVs indicated a total of 79.6 Mbp for the first comparison and 136.1 Mbp for the second one, while no SVs were detected for the third comparison. Interestingly, SVs differentiating cultivars and haplotypes affected similar numbers of coding genes.
CONCLUSIONS CONCLUSIONS
Our results suggest that SVs accumulation rate and their functional implications in 'Nebbiolo' genome are highly-dependent on the organizational level under study. SVs are abundant when comparing 'Nebbiolo' to a different cultivar or the two haplotypes of the same individual, while they turned absent between the two analysed clones.

Identifiants

pubmed: 35209840
doi: 10.1186/s12864-022-08389-9
pii: 10.1186/s12864-022-08389-9
pmc: PMC8867635
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

159

Informations de copyright

© 2022. The Author(s).

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Auteurs

Simone Maestri (S)

Department of Biotechnology, University of Verona, Strada Le Grazie 15, 37134, Verona, Italy.

Giorgio Gambino (G)

Institute for Sustainable Plant Protection, National Research Council (IPSP-CNR), Strada delle Cacce 73, 10135, Torino, Italy.

Giulia Lopatriello (G)

Department of Biotechnology, University of Verona, Strada Le Grazie 15, 37134, Verona, Italy.

Andrea Minio (A)

Department of Viticulture & Enology, University of California Davis, 595 Hilgard Lane, Davis, CA, 95616, USA.

Irene Perrone (I)

Institute for Sustainable Plant Protection, National Research Council (IPSP-CNR), Strada delle Cacce 73, 10135, Torino, Italy.

Emanuela Cosentino (E)

Department of Biotechnology, University of Verona, Strada Le Grazie 15, 37134, Verona, Italy.

Barbara Giovannone (B)

Department of Biotechnology, University of Verona, Strada Le Grazie 15, 37134, Verona, Italy.

Luca Marcolungo (L)

Department of Biotechnology, University of Verona, Strada Le Grazie 15, 37134, Verona, Italy.

Massimiliano Alfano (M)

Department of Biotechnology, University of Verona, Strada Le Grazie 15, 37134, Verona, Italy.

Stephane Rombauts (S)

Department of Bioinformatics and Systems Biology, Ghent University, Technologiepark 927, B-9052, Gent, Belgium.
VIB Center for Plant Systems Biology, 9052, Gent, Belgium.

Dario Cantu (D)

Department of Viticulture & Enology, University of California Davis, 595 Hilgard Lane, Davis, CA, 95616, USA.

Marzia Rossato (M)

Department of Biotechnology, University of Verona, Strada Le Grazie 15, 37134, Verona, Italy.

Massimo Delledonne (M)

Department of Biotechnology, University of Verona, Strada Le Grazie 15, 37134, Verona, Italy. massimo.delledonne@univr.it.

Luciano Calderón (L)

Instituto de Biología Agrícola de Mendoza (IBAM, CONICET-UNCuyo), Almirante Brown 500, M5528AHB. Chacras de Coria, Mendoza, Argentina. lcalderon@mendoza-conicet.gob.ar.

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Classifications MeSH