The globe artichoke genome has been recently sequenced [D. Scaglione, S. Reyes-Chin-Wo, A. Acquadro, L. Froenicke, E. Portis, C. Beitel, M. Tirone, R. Mauro, A. Lo Monaco, G. Mauromicale, P. Faccioli, L. Cattivelli, L. Rieseberg, R. Michelmore & S Lanteri. The genome sequence of the outbreeding globe artichoke constructed de novo incorporating a phase-aware low-pass sequencing strategy of F1 progeny. Sci. Rep. 6, 19427; doi: 10.1038/srep19427 (2016)]. It represents the first published genome sequence of a Compositae crop species fully available to the scientific community. The genome sequence has been unravelled by a consortium including the University of Torino (DISAFA, Plant Genetics and Breeding, Italy, team leader Sergio Lanteri), the University of California (The Genome Center, Davis, CA, USA, team leader Richard Michelmore) and the Università di Catania (Di3A, Italy, team leader Giovanni Mauromicale) in the framework of the Compositae Genome Project (CGP). The project started in 2011 and later on was joined by the University of British Columbia (Canada, team leader Loren Rieseberg) and Crea (Genomics Research Centre, Fiorenzuola d’Arda, Italy, team leader Luigi Cattivelli). The genome draft was assembled from ~133-fold next-generation sequencing data, into 13K scaffolds (N50= 125 Kbp, L50=1411), which represent 725 Mb of genomic sequence with a de novo prediction of 26,906 gene models. Thanks to a low coverage whole genome-sequencing of an F1 highly segregating mapping population, a dense genetic map based on the two-way pseudo test cross strategy, was built up and used for anchoring and orienting 73% of the assembled scaffolds in 17 reconstructed pseudomolecules. This was achieved thanks to the development of a novel pipeline, namely SOILoCo (Scaffold Ordering by Imputation with Low Coverage), which detects heterozygous regions and assigns parental haplotypes with low sequencing read depth (missing genotypes per block/type = 30-40%) and of unknown phase. In the manuscript major emphasis is given to the newly developed tool applied for genetically anchoring de novo assembled scaffolds without the availability of a validated reference genome, and whose accuracy and robustness was validated by aligning the two parental maps we independently generated. Although our pipeline was developed to analyze F1 progeny data, it may be also used for mapping with other progenies, such as F2, RILs, and BC populations. Actually, this scenario has not been approached in literature so far and can be of interest to a wide range of plant as well as animal genetics and genomics investigators. Bioinformatics analyses have also provided insights on the globe artichoke genome biology in terms of: i) protein coding genes along with distribution of gene families and inferences on speciation time, ii) miRNA genes and their repetitive context, iii) repetitive elements and insertion time.

Globe Artichoke Genome Database

Portis, E.;Comino, C.;Moglia, A.;Barchi, L.;Valentino, D;Milani, A;Lanteri, S.;Acquadro, A.
2016-01-01

Abstract

The globe artichoke genome has been recently sequenced [D. Scaglione, S. Reyes-Chin-Wo, A. Acquadro, L. Froenicke, E. Portis, C. Beitel, M. Tirone, R. Mauro, A. Lo Monaco, G. Mauromicale, P. Faccioli, L. Cattivelli, L. Rieseberg, R. Michelmore & S Lanteri. The genome sequence of the outbreeding globe artichoke constructed de novo incorporating a phase-aware low-pass sequencing strategy of F1 progeny. Sci. Rep. 6, 19427; doi: 10.1038/srep19427 (2016)]. It represents the first published genome sequence of a Compositae crop species fully available to the scientific community. The genome sequence has been unravelled by a consortium including the University of Torino (DISAFA, Plant Genetics and Breeding, Italy, team leader Sergio Lanteri), the University of California (The Genome Center, Davis, CA, USA, team leader Richard Michelmore) and the Università di Catania (Di3A, Italy, team leader Giovanni Mauromicale) in the framework of the Compositae Genome Project (CGP). The project started in 2011 and later on was joined by the University of British Columbia (Canada, team leader Loren Rieseberg) and Crea (Genomics Research Centre, Fiorenzuola d’Arda, Italy, team leader Luigi Cattivelli). The genome draft was assembled from ~133-fold next-generation sequencing data, into 13K scaffolds (N50= 125 Kbp, L50=1411), which represent 725 Mb of genomic sequence with a de novo prediction of 26,906 gene models. Thanks to a low coverage whole genome-sequencing of an F1 highly segregating mapping population, a dense genetic map based on the two-way pseudo test cross strategy, was built up and used for anchoring and orienting 73% of the assembled scaffolds in 17 reconstructed pseudomolecules. This was achieved thanks to the development of a novel pipeline, namely SOILoCo (Scaffold Ordering by Imputation with Low Coverage), which detects heterozygous regions and assigns parental haplotypes with low sequencing read depth (missing genotypes per block/type = 30-40%) and of unknown phase. In the manuscript major emphasis is given to the newly developed tool applied for genetically anchoring de novo assembled scaffolds without the availability of a validated reference genome, and whose accuracy and robustness was validated by aligning the two parental maps we independently generated. Although our pipeline was developed to analyze F1 progeny data, it may be also used for mapping with other progenies, such as F2, RILs, and BC populations. Actually, this scenario has not been approached in literature so far and can be of interest to a wide range of plant as well as animal genetics and genomics investigators. Bioinformatics analyses have also provided insights on the globe artichoke genome biology in terms of: i) protein coding genes along with distribution of gene families and inferences on speciation time, ii) miRNA genes and their repetitive context, iii) repetitive elements and insertion time.
2016
http://www.artichokegenome.unito.it/
Portis, E.; Portis, F.; Valente, L.; Comino, C.; Moglia, A.; Barchi, L.; Valentino, D; Milani, A; Lanteri, S.; Acquadro, A.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2318/1549128
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