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植物中的辐射杂种(RH)定位和HAPPY定位

Radiation hybrid (RH) and HAPPY mapping in plants.

作者信息

Riera-Lizarazu O, Vales M I, Kianian S F

机构信息

Department of Crop and Soil Science, Oregon State University, Corvallis, OR 97331-3002, USA.

出版信息

Cytogenet Genome Res. 2008;120(3-4):233-40. doi: 10.1159/000121072. Epub 2008 May 22.

Abstract

Radiation hybrid (RH) and HAPPY mapping are two technologies used in animal systems that have attracted the attention of the plant genetics community because they bridge the resolution gap between meiotic and BAC-based physical mapping that would facilitate the analysis of plant species lacking substantial genomics resources. Research has shown that the essence of these approaches can be applied and that a variety of strategies can be used to produce mapping panels. Mapping panels composed of live plants, protoplast fusion cultures, and sub-genomic DNA samples have been described. The resolution achievable by RH mapping panels involving live-plant derivatives of a monosomic maize (Zea mays) chromosome 9 addition in allohexaploid oat (Avena sativa), a monosomic chromosome 1D addition in allotetraploid durum wheat (Triticum turgidum), and interspecific hybrids between two tetraploid cotton species (G. hirsutum and G. barbadense), has been estimated to range from 0.6 to 6 Mb. On the other hand, a more comprehensive evaluation of one panel from durum wheat suggests that a higher mapping resolution (approximately 200 kb) is possible. In cases involving RH mapping panels based on barley (Hordeum vulgare)-tobacco (Nicotiana tabacum) protoplast fusions or a HAPPY mapping panel based on genomic DNA from Arabidopsis thaliana, the potential mapping resolution appears to be higher (50 to 200 kb). Despite these encouraging results, the application of either RH or HAPPY mapping in plants is still in the experimental phase and additional work is clearly needed before these methods are more routinely utilized.

摘要

辐射杂种(RH)图谱构建和HAPPY图谱构建是动物系统中使用的两种技术,它们引起了植物遗传学领域的关注,因为它们弥合了减数分裂图谱和基于细菌人工染色体(BAC)的物理图谱之间的分辨率差距,这将有助于分析缺乏大量基因组学资源的植物物种。研究表明,这些方法的核心可以应用,并且可以使用多种策略来构建作图群体。已经描述了由活植物、原生质体融合培养物和亚基因组DNA样本组成的作图群体。据估计,涉及异源六倍体燕麦(燕麦属)中添加单条玉米(玉米)9号染色体的活植物衍生物、异源四倍体硬粒小麦(普通小麦)中添加单条1D染色体以及两个四倍体棉花物种(陆地棉和海岛棉)之间的种间杂种的RH作图群体的分辨率范围为0.6至6兆碱基。另一方面,对一个来自硬粒小麦的群体进行的更全面评估表明,可能实现更高的作图分辨率(约200千碱基)。在涉及基于大麦(大麦属)-烟草(烟草属)原生质体融合的RH作图群体或基于拟南芥基因组DNA的HAPPY作图群体的情况下,潜在的作图分辨率似乎更高(50至200千碱基)。尽管有这些令人鼓舞的结果,但RH图谱构建或HAPPY图谱构建在植物中的应用仍处于实验阶段,在这些方法更常规地应用之前,显然还需要更多的工作。

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