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A draft genome of Prunus<3i//z//77'Karina' as a tool for genomic studies

机译:Prunus <3i // z // 77'karina的一个基因组作为基因组研究的工具

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Here we present the construction of a partial draft genome of the sweet cherry Prunus avium 'Karina' (2n=2x=16) taking advantage of the NGS technologies available and by implementing a de novo assembly strategy. The estimated assembly size was 352.5 Mb, comprising 904,813 contigs with a N50 of 9,188 bp. The contig merging process resulted in 898,488 scaffolds with a N50 of 13,235 bp and a maximum scaffold length of 419,819 bp. We performed a search for known genes with agronomical importance such asthe dormancy-associated MADS-box transcription factors (DAM) and two members of the eIF4G gene subfamily. The search results showed that six putative DAM genes are present in an apparent tandem array with a mean identity of 89.14% with the genomic sequences of Prunus persica. Similar results were achieved for the elFG genes, obtaining 89.76% of identity with the genomic sequences of Prunus persica and 60.36% of identity with the genomic sequences of Arabidopsis thaliana. With this we are hoping to obtain valuable data to perform genomic studies and to contribute to the better understanding of the genetic background of this cultivar and to obtain a tool to perform genomic studies in sweet cherry.
机译:在这里,我们展示了甜樱桃Prunus Avium'Karina'(2N = 2x = 16)的部分草案的构建,利用了可用的NGS技术,并通过实施De Novo装配策略。估计的组装大小为352.5 MB,包含904,813个ContIG,9,188bp的N50。 CONTIG合并过程导致898,488个支架,N50为13,235bp,最大支架长度为419,819bp。我们对具有农艺重要性的已知基因进行了寻找,这种休眠相关的疯狂箱转录因子(DAM)和eIF4G基因亚家族的两个成员。搜索结果表明,六个推定的坝基基因存在于明显的串联阵列中,其具有89.14%的平均同一性,具有Prunus persica的基因组序列。为ELFG基因达到了类似的结果,获得了89.76%的同一性,与拟南芥的基因组序列的蛋白质PERSICA的基因组序列和60.36%的同一性。通过这一点,我们希望获得有价值的数据来进行基因组研究,并有助于更好地了解该品种的遗传背景,并获得在甜樱桃中进行基因组研究的工具。

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