首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >Random amplified polymorphic DNA markers tightly linked to a gene for resistance to white pine blister rust in sugar pine.
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Random amplified polymorphic DNA markers tightly linked to a gene for resistance to white pine blister rust in sugar pine.

机译:随机扩增的多态性DNA标记与抗糖松中的白松水泡锈病的基因紧密相连。

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摘要

We have genetically mapped a gene for resistance to white pine blister rust (Cronartium ribicola Fisch.) in sugar pine (Pinus lambertiana Dougl.) by using an approach which relies on three factors: (i) the ability to assay for genetic markers in the haploid stage of the host's life cycle, using megagametophyte seed tissue; (ii) a simple and clearly defined pathosystem; and (iii) the use of random amplified polymorphic DNA (RAPD) markers that can be quickly and efficiently evaluated. Resistance to white pine blister rust in sugar pine is known to be controlled by a single dominant gene (R). Maternal segregation of R and dominant RAPD markers were scored simultaneously following collection of megagametophytes for DNA assays and seedling inoculation with C. ribicola. Bulked samples of haploid megagametophyte DNA from resistant and susceptible offspring of segregating full-sib and half-sib families were used to evaluate 800 random decanucleotide primers. Ten loci linked with the gene for resistance to white pine blister rust were identified and segregation data were obtained from five families. Six of the linked markers were within 5 centimorgans of the gene, and one marker was 0.9 centimorgan from R. These and other markers derived by this approach may provide starting points for map-based cloning of this important gene.
机译:我们使用一种依赖于以下三个因素的方法,对糖松(Pinus lambertiana Dougl。)中的白松水泡锈病(Cronartium ribicola Fisch。)的抗性进行了基因定位,方法是依靠三个因素:(i)在使用大型配子体种子组织的宿主生命周期的单倍体阶段; (ii)一个简单明确的病理系统; (iii)使用可以快速有效评估的随机扩增多态性DNA(RAPD)标记。已知对糖松中的白松水疱锈病的抵抗力由单个显性基因(R)控制。在收集大型配子体用于DNA测定和核糖衣原体接种后,同时对R和主要RAPD标记的母本隔离进行了评分。来自分离的全同胞和半同胞家族的抗性和易感后代的单倍体巨配子体DNA的大块样品用于评估800个随机十核苷酸引物。鉴定了与抗白松水泡锈病基因相关的十个基因座,并从五个家庭获得了隔离数据。六个连接的标记位于该基因的5个厘摩范围内,一个标记来自R的0.9个厘摩。通过此方法衍生的这些和其他标记可能为该重要基因的基于图谱的克隆提供起点。

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