Abstract

BackgroundCRISPR/Cas9 has been recently demonstrated as an effective and popular genome editing tool for modifying genomes of humans, animals, microorganisms, and plants. Success of such genome editing is highly dependent on the availability of suitable target sites in the genomes to be edited. Many specific target sites for CRISPR/Cas9 have been computationally identified for several annual model and crop species, but such sites have not been reported for perennial, woody fruit species. In this study, we identified and characterized five types of CRISPR/Cas9 target sites in the widely cultivated grape species Vitis vinifera and developed a user-friendly database for editing grape genomes in the future.ResultsA total of 35,767,960 potential CRISPR/Cas9 target sites were identified from grape genomes in this study. Among them, 22,597,817 target sites were mapped to specific genomic locations and 7,269,788 were found to be highly specific. Protospacers and PAMs were found to distribute uniformly and abundantly in the grape genomes. They were present in all the structural elements of genes with the coding region having the highest abundance. Five PAM types, TGG, AGG, GGG, CGG and NGG, were observed. With the exception of the NGG type, they were abundantly present in the grape genomes. Synteny analysis of similar genes revealed that the synteny of protospacers matched the synteny of homologous genes. A user-friendly database containing protospacers and detailed information of the sites was developed and is available for public use at the Grape-CRISPR website (http://biodb.sdau.edu.cn/gc/index.html).ConclusionGrape genomes harbour millions of potential CRISPR/Cas9 target sites. These sites are widely distributed among and within chromosomes with predominant abundance in the coding regions of genes. We developed a publicly-accessible Grape-CRISPR database for facilitating the use of the CRISPR/Cas9 system as a genome editing tool for functional studies and molecular breeding of grapes. Among other functions, the database allows users to identify and select multi-protospacers for editing similar sequences in grape genomes simultaneously.Electronic supplementary materialThe online version of this article (doi:10.1186/s12870-016-0787-3) contains supplementary material, which is available to authorized users.

Highlights

  • clustered regularly interspaced short palindromic repeats (CRISPR)/Cas9 has been recently demonstrated as an effective and popular genome editing tool for modifying genomes of humans, animals, microorganisms, and plants

  • Genomic distribution of protospacers and protospacer-adjacent motif (PAM) A total of 35,767,960 protospacer/PAMs were detected in the draft grape genome, and 63.18 % of them (22,597,817) were present at specific genomic locations

  • When the numbers of total and unique sites were compared, there were no significant differences in their distribution among the different chromosomes (Figs. 1b and c, respectively), suggesting that each chromosome had a similar level of protospacer/PAM abundance and the overall distribution was relatively uniform

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Summary

Introduction

CRISPR/Cas has been recently demonstrated as an effective and popular genome editing tool for modifying genomes of humans, animals, microorganisms, and plants. Success of such genome editing is highly dependent on the availability of suitable target sites in the genomes to be edited. We identified and characterized five types of CRISPR/Cas target sites in the widely cultivated grape species Vitis vinifera and developed a user-friendly database for editing grape genomes in the future. The Cas nuclease can be converted into a nicking enzyme to facilitate homology-directed repair with mutagenic activity [4] These properties of CRISPR/Cas make the system a valuable and versatile tool for many research applications [5, 6]. Several databases and web tools have been established to facilitate related studies [12,13,14]

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