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首页> 外文期刊>Journal of Applied Genetics >Identification and characterization of high-molecular-weight glutenin genes in Polish triticale cultivars by PCR-based DNA markers
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Identification and characterization of high-molecular-weight glutenin genes in Polish triticale cultivars by PCR-based DNA markers

机译:基于PCR的DNA标记鉴定和鉴定波兰小黑麦品种中的高分子量谷蛋白基因

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摘要

Molecular markers were used to identify the allele/gene composition of complex loci Glu-A1 and Glu-B1 of high-molecular-weight (HMW) glutenin subunits in triticale cultivars. Forty-six Polish cultivars of both winter and spring triticale were analysed with 7 PCR-based markers. Amplified DNA fragments of HMW glutenin Glu-1 genes were separated by agarose slab-gel electrophoresis. Differences between all 3 alleles at the locus Glu-A1 [Glu-A1a (encoding Ax1), 1b (Ax2*), and 1c (AxNull)], 4 alleles at Glu-B1-1 [Glu-B1-1a (Bx7), 1b (Bx7*), 1d (Bx6), 1ac (Bx6.8)], and 5 alleles at Glu-B1-2 [Glu-B1-2a (By8), 2b (By9), 2o (By8*), 2s (By18*), and 2z (By20*)] were revealed. In total, 16 allele combinations were observed. Molecular markers are particularly helpful in distinguishing the wheat Glu-A1a and Glu-A1b alleles from the rye Glu-R1a and Glu-R1b alleles in triticale genotypes, respectively, as well as subunits Bx7 from Bx7* and By8 from By8*, which could not be distinguished by SDS-PAGE. Novel glutenin subunits By18* and By20* (unique to triticale) were identified. HMW glutenin subunit combinations of Polish triticale cultivars, earlier identified by SDS-PAGE analyses, were verified by PCR-based DNA markers. Rapid identification of wheat Glu-1 alleles by molecular markers can be an efficient alternative to the standard separation procedure for early selection of useful triticale genotypes with good bread-making quality.
机译:分子标记用于鉴定小黑麦品种中高分子量(HMW)谷蛋白亚基的复杂基因座Glu-A1和Glu-B1的等位基因/基因组成。使用7种基于PCR的标记分析了冬季和春季黑小麦的46个波兰品种。 HMW谷蛋白Glu-1基因的扩增DNA片段通过琼脂糖平板凝胶电泳分离。 Glu-A1 [Glu-A1a(编码Ax1),1b(Ax2 *)和1c(AxNull)]基因座的所有3个等位基因之间的差异,Glu-B1-1 [Glu-B1-1a(Bx7))中的4个等位基因之间的差异,1b(Bx7 *),1d(Bx6),1ac(Bx6.8)]和Glu-B1-2的5个等位基因[Glu-B1-2a(By8),2b(By9),2o(By8 *),揭示了2s(By18 *)和2z(By20 *)]。总共观察到16个等位基因组合。分子标记特别有助于区分小麦的Glu-A1a和Glu-A1b等位基因与黑小麦基因型的黑麦Glu-R1a和Glu-R1b等位基因,以及Bx7 *和By8 *的亚基Bx7和Bx7 *。 SDS-PAGE不能区分。鉴定出新的谷蛋白亚基By18 *和By20 *(小黑麦独有)。波兰小黑麦品种的HMW谷蛋白亚基组合,早先通过SDS-PAGE分析鉴定,已通过基于PCR的DNA标记进行了验证。通过分子标记快速鉴定小麦Glu-1等位基因,可以作为标准分离程序的有效替代方法,以早期选择有用的黑小麦基因型,并具有良好的制面包质量。

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