首页> 外文会议>Biennial Meeting of the American^Society^of^Sugar^Beet^Technologists. >MOLECULAR CLONING OF X LOCUS AND MARKER-ASSISTED SELECTION OF NON-RESTORING ALLELE FOR OWEN CYTOPLASMIC MALE STERILITY
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MOLECULAR CLONING OF X LOCUS AND MARKER-ASSISTED SELECTION OF NON-RESTORING ALLELE FOR OWEN CYTOPLASMIC MALE STERILITY

机译:X基因座的分子克隆和标记辅助选择欧文细胞质雄性不育的非恢复等位基因

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According to Owen (1945), fully male sterile plants have the genotype (S)xxzz, while the remaining eight genotypes usually show varying degree of pollen fertility. To obtain offspring from male-sterile plants, which are themselves male sterile, cytoplasmic male sterility (CMS) plants must be pollinated by so-called maitainer plants (O-type), which carry the same nuclear genes as the male-sterile plants but with normal cytoplasm (N)xxzz. To develop marker-assisted selection (MAS) method, we investigated genetic variation at the Rfl locus (Matsuhira et al. 2012), one of the two i?/loci known in sugar beet. After digestion with Hindlll, DNAs from beet plants known to have a restoring Rfl allele yielded a range of hybridization patterns on Southern blots, indicating that Rfl is a multiallelic locus. However, 22 of 23 maintainer lines showed the same hybridization pattern. The sequences of the rfl coding regions of these 22 maintainer lines were found to be identical, confirming that they shared the same rfl allele (Moritani et al, 2013). Two PCR markers targeting a downstream intergenic sequence and the first intron of Rfl, respectively, were developed. The electrophoretic patterns of both markers showed multiple Rfl alleles. One of these alleles, named the dd(L) type, was associated with the maintainer genotype.
机译:根据欧文(1945),全雄性无菌植物具有基因型XXZZ,而剩余的8个基因型通常会显示出不同程度的花粉生育率。为了从本身是雄性无菌,细胞质雄性不育(CMS)植物必须通过所谓的Maitainer植物(O型)授粉,其携带与雄性无菌植物相同的核基因,但是雄性不育植物的后代具有正常细胞质(n)xxzz。为了开发标记辅助选择(MAS)方法,我们调查了RFL基因座(Matsuhira等,2012)的遗传变异,其中两个I中的一个?/甜菜中已知的基因座。在用HindIMLL消化后,来自已知具有恢复RFL等位基因的甜菜植物的DNA在南部印迹上产生了一系列杂交模式,表明RFL是多晶轨迹。然而,22条维护系列中的22条显示出相同的杂交模式。发现这22个维护系的RFL编码区域的序列是相同的,确认它们共享相同的RFL等位基因(Moritani等,2013)。鉴定靶向下游亚基因序列和RFL的第一个内含子的两个PCR标记物。两个标记的电泳模式显示多个RFL等位基因。其中一个名为DD(L)类型的等位基因之一与维护者基因型相关联。

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