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Positional cloning of the rice male sterility gene ms-IR36, widely used in the inter-crossing phase of recurrent selection schemes

机译:水稻雄性不育基因ms-IR36的位置克隆,广泛用于轮回选择方案的杂交阶段

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The monogenetic recessive male-sterile gene ms-IR36 is widely used to facilitate the inter-crossing phase of recurrent selection in rice (Oryza sativa), but its segregation within the progeny disturbs other breeding phases. Marker-assisted early identification of msms and Msms seedlings would help overcome this drawback. Using successively bulked segregant analysis and large F2 populations, we mapped the ms-IR36 gene to a 33-kb region on the short arm of chromosome 2 that includes 10 candidate genes. Sequencing of these candidates together with checking rice genome annotations and expression databases allowed the target to be narrowed down to one candidate gene already isolated and characterized as the tapetum degeneration retardation (TDR) gene and reported to be involved in tapetal programmed cell death. Comparison of the sequence of the TDR gene between male-sterile (MS) and male-fertile (MF) IR36 plants detected one non-synonymous nucleotide substitution affecting the active domain of the encoded protein. Perfect co-segregation was observed between polymorphism at this nucleotide (SNP) and the MS/MF phenotype of 946 F2 plants. Spatial modelling of the active domain of the candidate protein reinforced the candidate status of the only SNP identified. Histological characterization of anther development in MS IR36 revealed defects identical to the ones observed in mutants used for the isolation and characterization of the TDR gene: delayedon-degradation of tapetum tissue and collapse of the haploid microspores. We concluded that ms-IR36 corresponded to the TDR gene with a different mutation from the earlier one described in the same gene. No significant linkage drag was associated with ms-IR36. A SNP-based marker that enables simple early identification of MS plants and MF plants with the Msms genotype was designed.
机译:单基因隐性雄性不育基因ms-IR36被广泛用于促进水稻(Oryza sativa)轮回选择的杂交期,但其后代中的分离干扰了其他育种期。标记辅助的msms和Msms幼苗的早期识别将有助于克服此缺点。使用连续大量的分离子分析和较大的F2种群,我们将ms-IR36基因定位到2号染色体短臂上的33kb区域,该区域包括10个候选基因。通过对这些候选基因的测序以及对水稻基因组注释和表达数据库的检查,可以将靶标缩小为一个已经分离并表征为绒毡层退化阻滞(TDR)基因并据报道参与绒毡层编程性细胞死亡的候选基因。雄性不育(MS)和雄性可育(MF)IR36植物之间的TDR基因序列比较发现一种非同义核苷酸取代影响编码蛋白的活性域。在该核苷酸的多态性(SNP)和946 F2植物的MS / MF表型之间观察到完美的共分离。候选蛋白活性域的空间建模增强了所鉴定的唯一SNP的候选状态。 MS IR36中花药发育的组织学特征表明,与用于分离和表征TDR基因的突变体中观察到的缺陷相同:绒毡层组织延迟/未降解以及单倍体小孢子塌陷。我们得出的结论是,ms-IR36对应于TDR基因,其突变与同一基因中描述的TDR基因不同。没有明显的连锁阻力与ms-IR36相关。设计了一种基于SNP的标记,该标记可以简单地早期识别具有Msms基因型的MS植物和MF植物。

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