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The genome sequence of sweet cherry (Prunus avium) for use in genomics-assisted breeding

We determined the genome sequence of sweet cherry (Prunus avium) using next-generation sequencing technology. The total length of the assembled sequences was 272.4 Mb, consisting of 10,148 scaffold sequences with an N50 length of 219.6 kb. The sequences covered 77.8% of the 352.9 Mb sweet cherry gen...

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Autores principales: Shirasawa, Kenta, Isuzugawa, Kanji, Ikenaga, Mitsunobu, Saito, Yutaro, Yamamoto, Toshiya, Hirakawa, Hideki, Isobe, Sachiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5737369/
https://www.ncbi.nlm.nih.gov/pubmed/28541388
http://dx.doi.org/10.1093/dnares/dsx020
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author Shirasawa, Kenta
Isuzugawa, Kanji
Ikenaga, Mitsunobu
Saito, Yutaro
Yamamoto, Toshiya
Hirakawa, Hideki
Isobe, Sachiko
author_facet Shirasawa, Kenta
Isuzugawa, Kanji
Ikenaga, Mitsunobu
Saito, Yutaro
Yamamoto, Toshiya
Hirakawa, Hideki
Isobe, Sachiko
author_sort Shirasawa, Kenta
collection PubMed
description We determined the genome sequence of sweet cherry (Prunus avium) using next-generation sequencing technology. The total length of the assembled sequences was 272.4 Mb, consisting of 10,148 scaffold sequences with an N50 length of 219.6 kb. The sequences covered 77.8% of the 352.9 Mb sweet cherry genome, as estimated by k-mer analysis, and included >96.0% of the core eukaryotic genes. We predicted 43,349 complete and partial protein-encoding genes. A high-density consensus map with 2,382 loci was constructed using double-digest restriction site–associated DNA sequencing. Comparing the genetic maps of sweet cherry and peach revealed high synteny between the two genomes; thus the scaffolds were integrated into pseudomolecules using map- and synteny-based strategies. Whole-genome resequencing of six modern cultivars found 1,016,866 SNPs and 162,402 insertions/deletions, out of which 0.7% were deleterious. The sequence variants, as well as simple sequence repeats, can be used as DNA markers. The genomic information helps us to identify agronomically important genes and will accelerate genetic studies and breeding programs for sweet cherries. Further information on the genomic sequences and DNA markers is available in DBcherry (http://cherry.kazusa.or.jp (8 May 2017, date last accessed)).
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spelling pubmed-57373692018-01-08 The genome sequence of sweet cherry (Prunus avium) for use in genomics-assisted breeding Shirasawa, Kenta Isuzugawa, Kanji Ikenaga, Mitsunobu Saito, Yutaro Yamamoto, Toshiya Hirakawa, Hideki Isobe, Sachiko DNA Res Full Papers We determined the genome sequence of sweet cherry (Prunus avium) using next-generation sequencing technology. The total length of the assembled sequences was 272.4 Mb, consisting of 10,148 scaffold sequences with an N50 length of 219.6 kb. The sequences covered 77.8% of the 352.9 Mb sweet cherry genome, as estimated by k-mer analysis, and included >96.0% of the core eukaryotic genes. We predicted 43,349 complete and partial protein-encoding genes. A high-density consensus map with 2,382 loci was constructed using double-digest restriction site–associated DNA sequencing. Comparing the genetic maps of sweet cherry and peach revealed high synteny between the two genomes; thus the scaffolds were integrated into pseudomolecules using map- and synteny-based strategies. Whole-genome resequencing of six modern cultivars found 1,016,866 SNPs and 162,402 insertions/deletions, out of which 0.7% were deleterious. The sequence variants, as well as simple sequence repeats, can be used as DNA markers. The genomic information helps us to identify agronomically important genes and will accelerate genetic studies and breeding programs for sweet cherries. Further information on the genomic sequences and DNA markers is available in DBcherry (http://cherry.kazusa.or.jp (8 May 2017, date last accessed)). Oxford University Press 2017-10 2017-05-25 /pmc/articles/PMC5737369/ /pubmed/28541388 http://dx.doi.org/10.1093/dnares/dsx020 Text en © The Author 2017. Published by Oxford University Press on behalf of Kazusa DNA Research Institute. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Full Papers
Shirasawa, Kenta
Isuzugawa, Kanji
Ikenaga, Mitsunobu
Saito, Yutaro
Yamamoto, Toshiya
Hirakawa, Hideki
Isobe, Sachiko
The genome sequence of sweet cherry (Prunus avium) for use in genomics-assisted breeding
title The genome sequence of sweet cherry (Prunus avium) for use in genomics-assisted breeding
title_full The genome sequence of sweet cherry (Prunus avium) for use in genomics-assisted breeding
title_fullStr The genome sequence of sweet cherry (Prunus avium) for use in genomics-assisted breeding
title_full_unstemmed The genome sequence of sweet cherry (Prunus avium) for use in genomics-assisted breeding
title_short The genome sequence of sweet cherry (Prunus avium) for use in genomics-assisted breeding
title_sort genome sequence of sweet cherry (prunus avium) for use in genomics-assisted breeding
topic Full Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5737369/
https://www.ncbi.nlm.nih.gov/pubmed/28541388
http://dx.doi.org/10.1093/dnares/dsx020
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