Development and validation of CAPS-marker associated with the Rf2 gene in sorghum (Sorghum bicolor (L.) Moench)

Q3 Agricultural and Biological Sciences
E. Radchenko, N. Alpatieva, Yu.I. Karabitsina, M. K. Ryazanova, E. B. Kuznetsova, O. Romanova, I. Anisimova
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引用次数: 0

Abstract

Background. The development of heterotic hybrids based on cytoplasmic male sterility (CMS) is the leading strategy in breeding sorghum (Sorghum bicolor (L.) Moench). The trait of pollen fertility restoration in forms with CMS A1 (milo), predominantly used in sorghum breeding, is determined by at least two dominant complementary genes Rf1 and Rf2, and also gene Rf5. The development of accessible molecular markers of sorghum Rf genes is highly relevant for hybrid breeding, since they can significantly accelerate the process of creating female sterile forms (A lines), sterility maintainers (B lines) and pollen fertility restorers (R lines).Material and methods. The studied material included 36 sorghum accessions from the VIR collection, which differed by the ability to restore pollen fertility in forms with A1-type CMS. The nucleotide polymorphism of 935 bp fragments of the PPR genes Sobic.002G057050, Sobic.002G054100, and Sobic.002G054200 located at the chromosome 2 was studied.Results. The fragments obtained with the use of a pair of 2459403fw and 2459403 primers were 935 bp long and included parts of three genes: Sobic.002G057050, Sobic.002G054100, Sobic.002G054200. For identifying the sequence variant Sobic.002G057050-1090 associated with the Rf2 gene, Tru9 I restrictase was chosen, which allows obtaining a 572 bp fragment unique for all the studied R lines. Such a marker was found in 10 sorghum lines from West China and Kyrgyzstan, which are widely used in breeding as fertility restorers. The fragment was found neither in three lines with sterile cytoplasm and their fertile analogues, nor in 7 accessions of kafir sorghum, which lacked functional alleles of Rf genes.Conclusions. It has been demonstrated that the marker can be used for selection and checking purity of R and B/A lines. It is also applicable for verifying hybridity of F1 seeds and analyzing hybrid populations from crosses of R lines 924-4, 928-1, 929-3, 931-1, 933-1/6, 1237-3, 1243-2, 1251, 1150-1, F10BC2 with A lines Nizkorosloe 81s, А-83 and А-10598. It may be suggested that the ability to restore pollen fertility in R lines, which lack the marker CAPS- 572, is determined by another Rf gene. The studied 935 bp fragment of Sobic.002G057050 harbours 22 SNP, therefore the development of CAPS-markers for their identification and differentiation can be promising.
高粱(sorghum bicolor (L.)) Rf2基因相关caps标记的开发与验证Moench)
背景。基于细胞质雄性不育(CMS)的杂种优势培育是高粱育种的主导策略。Moench)。主要用于高粱育种的具有CMS A1 (milo)的花粉育性恢复性状是由至少两个显性互补基因Rf1和Rf2以及基因Rf5决定的。可接近的高粱Rf基因分子标记的开发与杂交育种密切相关,因为它们可以显著加快雌性不育型(A系)、不育保持型(B系)和花粉育性恢复系(R系)的形成过程。材料和方法。研究材料包括来自VIR收集的36份高粱材料,这些材料在a1型CMS形式中恢复花粉育性的能力不同。研究了PPR基因Sobic.002G057050、Sobic.002G054100和Sobic.002G054200位于2号染色体上935 bp片段的核苷酸多态性。使用一对2459403fw和2459403引物获得的片段长935 bp,包含三个基因的部分:Sobic.002G057050, Sobic.002G054100, Sobic.002G054200。为了鉴定与Rf2基因相关的序列变异Sobic.002G057050-1090,选择了tru9i限制性酶,获得了所有R系所特有的572 bp片段。在中国西部和吉尔吉斯斯坦的10个高粱品系中发现了该标记,作为育性恢复系广泛应用于育种。该片段未在3个细胞质不育系及其可育类似物中发现,也未在缺少Rf基因功能等位基因的7份卡菲尔高粱材料中发现。结果表明,该标记可用于R系和B/A系的筛选和纯度检测。也可用于验证F1种子的杂种性,分析R系924-4、928-1、929-3、931-1、933-1/6、1237-3、1243-2、1251、1150-1、F10BC2与A系Nizkorosloe 81s、А-83和А-10598的杂交群体。这可能表明,缺少CAPS- 572标记的R系恢复花粉育性的能力是由另一个Rf基因决定的。Sobic.002G057050 935 bp的片段包含22个SNP,因此开发caps标记对其进行鉴定和分化是有前景的。
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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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