Polymorphism of microsatellite markers linked with Rf1 and Pl5/Pl8 loci in sunflower Helianthus annuus L.

Q3 Agricultural and Biological Sciences Plant breeding and biotechnology Pub Date : 2022-01-07 DOI:10.30901/2658-6266-2021-4-o1
Yu.I. Karabitsina, N. Alpatieva, E. B. Kusnetsova, V. Gavrilova, N. V. Titov, E. Radchenko, I. Anisimova
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Abstract

Background. Microsatellite (SSR) markers are an effective tool for certifying collections of plant genetic resources, as well as for identifying genes that determine valuable biological and agronomic traits. The knowledge of their polymorphism is important for characterizing genetic diversity within the sunflower (Helianthus annuus L.) collection. The present study was aimed at analyzing nucleotide polymorphism of SSR-markers linked with the genes for fertility restoration (Rf1) and downy mildew resistance (Pl5/Pl8). Materials and methods. The material included 84 self-pollinated lines of VIR sunflower genetic collection, F1 and F2 hybrids from crosses between fertile lines VIR 365 and RIL130, and offspring from test crosses. Polymorphism of SSR markers ORS224, ORS511, ORS799 and НА4011 was studied by means of PCR analysis. To determine the microsatellite structure and variability, the amplified fragments were cloned and sequenced. Results. The unique alleles which differed from the typical ones (characteristic for most genotypes) were revealed in the ORS224 marker locus of four lines, and the unique alleles in the ORS511 locus were observed in 10 lines. The ORS511 unique allele of line VIR 365 included two 161 and 240 bp fragments, while line RIL130 was characterized by a typical 159 bp fragment. The profiles of typical and unique markers were inherited as allelic variants of the same locus in F2 of (VIR 365 × RIL130) and a population from VIR 111A × (VIR 365 × RIL130). The nucleotide sequences of unique alleles differed from typical allelic variants in the length and number of repeat units (GA in ORS224 and AT/GT in ORS511), and also by the presence of indels and nucleotide substitutions. Differences in length of НА4011 marker 240 and 200 bp allele variants were caused by 80, 47 and 44 bp indels. Conclusions. A number of lines in the VIR sunflower genetic collection are marked by the unique alleles of microsatellite loci ORS224 and ORS511, which differ from the frequently occurring variants in the length and number of repeat units, as well as in the presence of indels and nucleotide substitutions. Polymorphism of allele variants of HA4011 microsatellite is associated with the presence of indels of 80, 47 and 4 bp.
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向日葵Rf1和Pl5/Pl8位点微卫星标记多态性研究
背景。微卫星(SSR)标记是鉴定植物遗传资源的有效工具,也是鉴定决定有价值的生物和农艺性状的基因的有效工具。了解它们的多态性对向日葵(Helianthus annuus L.)种质资源的遗传多样性具有重要意义。本研究旨在分析与育性恢复基因(Rf1)和抗霜霉病基因(Pl5/Pl8)相关的ssr标记的核苷酸多态性。材料和方法。材料包括84个VIR向日葵自花授粉系、VIR 365和RIL130可育系杂交的F1和F2杂交种,以及试验杂交后代。采用PCR方法对SSR标记ORS224、ORS511、ORS799和НА4011进行多态性分析。为了确定微卫星的结构和变异,对扩增片段进行了克隆和测序。结果。在4个品系的ORS224标记位点上发现了与典型位点不同的独特等位基因(大多数基因型的特征),在10个品系的ORS511标记位点上发现了独特等位基因。VIR 365系的ORS511独特等位基因包含两个161和240 bp的片段,而RIL130系的ORS511独特等位基因包含一个159 bp的片段。在VIR 365 × RIL130的F2和VIR 111A × (VIR 365 × RIL130)的一个群体中,典型和独特的标记谱作为同一位点的等位变异遗传。独特等位基因的核苷酸序列在长度和重复单元数(ORS224的GA和ORS511的AT/GT)上与典型等位基因变异不同,也存在索引和核苷酸替换。НА4011标记240和200 bp等位基因变异的长度差异由80、47和44 bp引起。结论。VIR向日葵遗传集合中的许多系都具有微卫星位点ORS224和ORS511的独特等位基因,这些等位基因在重复单元的长度和数量以及存在索引和核苷酸替换方面与频繁发生的变异不同。HA4011微卫星等位基因变异的多态性与80、47和4 bp位点的存在有关。
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来源期刊
Plant breeding and biotechnology
Plant breeding and biotechnology Agricultural and Biological Sciences-Plant Science
CiteScore
2.30
自引率
0.00%
发文量
18
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