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通过单亲单倍体实现四倍体马铃薯中耦合连锁标记的最大化

Maximization of Markers Linked in Coupling for Tetraploid Potatoes via Monoparental Haploids.

作者信息

Bartkiewicz Annette M, Chilla Friederike, Terefe-Ayana Diro, Lübeck Jens, Strahwald Josef, Tacke Eckhard, Hofferbert Hans-Reinhard, Linde Marcus, Debener Thomas

机构信息

Department of Molecular Plant Breeding, Institute of Plant Genetics, Leibniz University Hannover, Hannover, Germany.

Westhoff, Südlohn, Germany.

出版信息

Front Plant Sci. 2018 May 7;9:620. doi: 10.3389/fpls.2018.00620. eCollection 2018.

Abstract

Haploid potato populations derived from a single tetraploid donor constitute an efficient strategy to analyze markers segregating from a single donor genotype. Analysis of marker segregation in populations derived from crosses between polysomic tetraploids is complicated by a maximum of eight segregating alleles, multiple dosages of the markers and problems related to linkage analysis of marker segregation in repulsion. Here, we present data on two monoparental haploid populations generated by prickle pollination of two tetraploid cultivars with and genotyped with the 12.8 k SolCAP single nucleotide polymorphism (SNP) array. We show that in a population of monoparental haploids, the number of biallelic SNP markers segregating in linkage to loci from the tetraploid donor genotype is much larger than in putative crosses of this genotype to a diverse selection of 125 tetraploid cultivars. Although this strategy is more laborious than conventional breeding, the generation of haploid progeny for efficient marker analysis is straightforward if morphological markers and flow cytometry are utilized to select true haploid progeny. The level of introgressed fragments from , the haploid inducer, is very low, supporting its suitability for genetic analysis. Mapping with single-dose markers allowed the analysis of quantitative trait loci (QTL) for four phenotypic traits.

摘要

源自单个四倍体供体的单倍体马铃薯群体是分析从单个供体基因型分离的标记的有效策略。多体四倍体之间杂交产生的群体中标记分离的分析因最多八个分离等位基因、标记的多个剂量以及与排斥中标记分离的连锁分析相关的问题而变得复杂。在这里,我们展示了通过用 对两个四倍体品种进行针刺授粉产生并使用 12.8 k SolCAP 单核苷酸多态性(SNP)阵列进行基因分型的两个单亲单倍体群体的数据。我们表明,在单亲单倍体群体中,与四倍体供体基因型的基因座连锁分离的双等位基因 SNP 标记的数量比该基因型与 125 个不同四倍体品种的假定杂交中要多得多。尽管这种策略比传统育种更费力,但如果利用形态学标记和流式细胞术来选择真正的单倍体后代,那么为了进行有效的标记分析而产生单倍体后代是直接可行的。单倍体诱导剂 渗入片段的水平非常低,这支持了它适用于遗传分析。用单剂量标记进行图谱绘制允许对四个表型性状进行数量性状位点(QTL)分析。

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