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基于合成参考序列的高通量测序在日本李中的基因座基因型鉴定。

-Locus Genotyping in Japanese Plum by High Throughput Sequencing Using a Synthetic -Loci Reference Sequence.

机构信息

Departamento de Ciencia Vegetal, Centro de Investigación y Tecnología Agroalimentaria de Aragón (CITA), Avda Montañana 930, 50059 Zaragoza, Spain.

Área de Fruticultura Mediterránea, CICYTEX-Centro de Investigación 'Finca La Orden-Valdesequera', A-V, KM 372, Guadajira, 06187 Badajoz, Spain.

出版信息

Int J Mol Sci. 2023 Feb 15;24(4):3932. doi: 10.3390/ijms24043932.

Abstract

Self-incompatibility in species is governed by a single locus consisting of two highly multi-allelic and tightly linked genes, one coding for an F-box protein-i.e., SFB in - controlling the pollen specificity and one coding for an gene controlling the pistil specificity. Genotyping the allelic combination in a fruit tree species is an essential procedure both for cross-based breeding and for establishing pollination requirements. Gel-based PCR techniques using primer pairs designed from conserved regions and spanning polymorphic intronic regions are traditionally used for this task. However, with the great advance of massive sequencing techniques and the lowering of sequencing costs, new genotyping-by-sequencing procedures are emerging. The alignment of resequenced individuals to reference genomes, commonly used for polymorphism detection, yields little or no coverage in the -locus region due to high polymorphism between different alleles within the same species, and cannot be used for this purpose. Using the available sequences of Japanese plum -loci concatenated in a rosary-like structure as synthetic reference sequence, we describe a procedure to accurately genotype resequenced individuals that allowed the analysis of the -genotype in 88 Japanese plum cultivars, 74 of them are reported for the first time. In addition to unraveling two new -alleles from published reference genomes, we identified at least two -alleles in 74 cultivars. According to their -allele composition, they were assigned to 22 incompatibility groups, including nine new incompatibility groups reported here for the first time (XXVII-XXXV).

摘要

自交不亲和性在 物种中由一个单一基因座控制,该基因座由两个高度多等位基因和紧密连锁的基因组成,一个编码 F-box 蛋白,即 - 中的 SFB,控制花粉特异性,另一个编码 基因,控制雌蕊特异性。对果树物种的等位基因组合进行基因分型是基于杂交的育种和建立授粉要求的必要程序。传统上,使用从保守区域设计并跨越多态性内含子区域的引物对的基于凝胶的 PCR 技术用于此任务。然而,随着大规模测序技术的巨大进步和测序成本的降低,新的测序基因分型程序正在出现。将重测序个体与参考基因组进行比对,通常用于检测多态性,由于同一物种内不同等位基因之间的高度多态性,在 - 基因座区域几乎没有或没有覆盖,因此不能用于此目的。我们使用串联成串珠状结构的日本李 - 基因座的可用序列作为合成参考序列,描述了一种准确基因分型重测序个体的程序,该程序允许分析 88 个日本李品种的 - 基因型,其中 74 个品种是首次报道的。除了从已发表的参考基因组中揭示两个新的 - 等位基因外,我们还在 74 个品种中鉴定出至少两个 - 等位基因。根据它们的 - 等位基因组成,它们被分配到 22 个不亲和组,其中包括这里首次报道的 9 个新的不亲和组(XXVII-XXXV)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21e9/9960950/65452d1df28b/ijms-24-03932-g001.jpg

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