P417
Improvement of the Grapevine Genome Assembly

Date: Monday, January 13, 2014
Room: Grand Exhibit Hall
Anne-Francoise Adam-Blondon , INRA - URGI, Versailles, France
Aurélie Canaguier , INRA-URGV, Evry, France
Simone Scalabrin , Istituto di Genomica Applicata, Udine, Italy
Marie-Christine Le Paslier , INRA, US1279 Etude du Polymorphisme des Génomes Végétaux, CEA-IG / Centre National de Génotypage, Evry, France
Eric Duchene , INRA-SVQV, COLMAR, France
Nacer Mohellibi , INRA - URGI, Versailles, France
Aurélie Bérard , INRA, US1279 Etude du Polymorphisme des Génomes Végétaux, CEA-IG / Centre National de Génotypage, Evry, France
Aurélie Chauveau , INRA, US1279 Etude du Polymorphisme des Génomes Végétaux, CEA-IG / Centre National de Génotypage, Evry, France
Jean-Michel Boursiquot , SupAgro Montpellier-AGAP, Montapellier, France
Gabriele Di Gaspero , IGA, Udine, Italy
Ludger Hausmann , JKI, Siebeldingen, Germany
Jose-Miguel Martinez-Zapater , ICVV, Logroño, Spain
Michele Morgante , IGA Istituto di Genomica Applicata, Udine, Italy
The current chromosome assembly of the grapevine reference genome is under improvement using two strategies. First several maps have been densified using SNP markers developed both from a classic Sanger re-sequencing of the parents and from the re-sequencing of a panel of diversity in the Vitaceae genome to develop a 18K genotyping chip (http://urgi.versailles.inra.fr/Species/Vitis/GrapeReSeq_Illumina_20K). This allowed to develop 6 parental genetic maps that were aligned on the scaffold of the genome assembly (www.ncbi.nlm.nih.gov/assembly/317318/; urgi.versailles.inra.fr/Species/Vitis/Data-Sequences ). Second, mate paire sequences were generated from 3kb DNA fragments of V. vinifera cv. Kishmish vatkana and used for further scaffolding. We were able to improve from 85% to 89% the percentage of the ordered sequence along the chromosomes and to improve the overall orientation of the scaffolds along the chromosomes.

Acknowledgements: Grant Plant-KBBE-2008-GrapeReSeq