2017
DOI: 10.1038/ng.3886
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High-quality de novo assembly of the apple genome and methylome dynamics of early fruit development

Abstract: Using the latest sequencing and optical mapping technologies, we have produced a high-quality de novo assembly of the apple (Malus domestica Borkh.) genome. Repeat sequences, which represented over half of the assembly, provided an unprecedented opportunity to investigate the uncharacterized regions of a tree genome; we identified a new hyper-repetitive retrotransposon sequence that was over-represented in heterochromatic regions and estimated that a major burst of different transposable elements (TEs) occurre… Show more

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Cited by 678 publications
(698 citation statements)
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References 80 publications
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“…Additionally, 26 460 genes in the male genome were predicted and supported by transcripts from the male flowers (Table ), of which 3079 genes were not covered by the female gene set, so the total gene number was 32 493 for both female and male. The number of genes was similar to that found in peach (Verde et al ., ) and pomegranate (Yuan et al ., ), but considerably lower than that in apple (Daccord et al ., ). A total of 26 316 (89.5%) genes in the female had substantial homology with those in public databases (Table S10).…”
Section: Resultsmentioning
confidence: 97%
“…Additionally, 26 460 genes in the male genome were predicted and supported by transcripts from the male flowers (Table ), of which 3079 genes were not covered by the female gene set, so the total gene number was 32 493 for both female and male. The number of genes was similar to that found in peach (Verde et al ., ) and pomegranate (Yuan et al ., ), but considerably lower than that in apple (Daccord et al ., ). A total of 26 316 (89.5%) genes in the female had substantial homology with those in public databases (Table S10).…”
Section: Resultsmentioning
confidence: 97%
“…BAC end sequencing was performed by an external service (BIOFAB Research, Rome, Italy) starting from 20 μg of purified plasmids and 24 pmol/ μl of either the Sp6 (5′-AGGTGACACTATAGAATACTC-3′) or T7 (5′-TAATACGACTCACTATAGGG-3′) primers. The sequences were analyzed with the Codon Code Aligner software (version 7.0.1) and alignment was performed both on the 'Golden Delicious' v 1.0 genome (Velasco et al 2010) with the BLASTN tool on the Genome Database of Rosaceae (GDR) website (https://www.rosaceae.org) and on the newly released sequence of the doubled-haploid genome of 'Golden Delicious' (GDDH13) available at https://iris.angers.inra.fr/ gddh13 (Daccord et al 2017).…”
Section: Bac Library Screening and Bac End Sequencingmentioning
confidence: 99%
“…Through the development of new polymorphic markers, the resistant Dp-fl locus was restricted to a physical region of 95 Kb. Structural and functional annotations were performed by comparing the 'Florina' resistant sequence with the homologous region of the 'Golden Delicious' doubled-haploid (GDDH13) genome sequence (Daccord et al 2017). The identification of four candidate resistance genes within the Dp-fl window is discussed.…”
Section: Communicated By E Dirlewangermentioning
confidence: 99%
“…Phenotypic scores for individuals with replicates were averaged for the purposes of QTL analyses. Physical locations for identified QTL that were consistent across years were retrieved by blasting SNP sequences at QTL regions to version 1.1 of the GDDH13 apple reference genome (Daccord et al 2017, https://iris.angers.inra. fr/gddh13/) with BLASTN 2.2.25+ (Zhang et al 2000).…”
Section: Qtl Analysesmentioning
confidence: 99%