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First-generation SNP/InDel markers tagging loci for pathogen resistance in the potato genome

机译:第一代SNP / Indel标记标记用于马铃薯基因组的病原体抵抗的基因座

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A panel of 17 tetraploid and 11 diploid potato genotypes was screened by comparative sequence analysis of polymerase chain reaction (PCR) products for single nucleotide polymorphisms (SNPs) and insertion-deletion polymorphisms (InDels), in regions of the potato genome where genes for qualitative and/or quantitative resistance to different pathogens have been localized. Most SNP and InDel markers were derived from bacterial artificial chromosome (BAC) insertions that contain sequences similar to the family of plant genes for pathogen resistance having nucleotide-binding-site and leucine-rich-repeat domains (NBS-LRR-type genes). Forty-four such NBS-LRR-type genes containing BAC-insertions were mapped to 14 loci, which tag most known resistance quantitative trait loci (QTL) in potato. Resistance QTL not linked to known resistance-gene-like (RGL) sequences were tagged with other markers. In total, 78 genomic DNA fragments with an overall length of 31 kb were comparatively sequenced in the panel of 28 genotypes. 1498 SNPs and 127 InDels were identified, which corresponded, on average, to one SNP every 21 base pairs and one InDel every 243 base pairs. The nucleotide diversity of the tetraploid genotypes (pi = 0.72 x 10(-3)) was lower when compared with diploid genotypes (pi = 2.31 x 10(-3)). RGL sequences showed higher nucleotide diversity when compared with other sequences, suggesting evolution by divergent selection. Information on sequences, sequence similarities, SNPs and InDels is provided in a database that can be queried via the Internet.
机译:通过聚合酶链式反应(PCR)产物的比较序列分析(PCR)产物为单核苷酸多态性(SNP)和插入缺失多态性(Indels),在马铃薯基因组的区域中,筛选了17个四倍体和11个二倍体马铃薯基因型的面板。和/或对不同病原体的定量抗性已经局部化。大多数SNP和诱导标记源自细菌人工染色体(BAC)插入,其含有与植物基因系列类似的序列,用于具有核苷酸结合位点和富含亮氨酸富含的重复域(NBS-LRR型基因)。将含有Bac插入的44个这样的NBS-LRR型基因映射到14个基因座,该基因座标记马铃薯中最令人所知的抗性定量性状基因座(QTL)。与已知抗性基因样(RGL)序列的抗性QTL与其他标记标记。总共78个基因组DNA片段在28种基因型的面板中相对测序。鉴定了1498个SNP和127个吲哚,平均相当于每21个碱基对的一个SNP,每243个碱基对。与二倍体基因型相比(PI = 2.31×10(-3))相比,四倍体基因型的核苷酸多样性(PI = 0.72×10(-3))较低。与其他序列相比,RGL序列显示出更高的核苷酸多样性,提示通过发散选择的演变。有关序列,序列相似度,SNP和indels的信息在可以通过因特网查询的数据库中提供。

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