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Molecular Markers for Genetic Fidelity Assay ofTissue Cultured Crops

机译:组织培养农作物遗传保真度测定的分子标记

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Tissue culture techniques are being widely used for the production of large-scale disease-free planting material aseptically on artificial media within a lesser span of time and space. This technique has gained tremendous popularity in recent days for the commercial production of several clonally propagated plants such as banana, bamboo, pointed guard, seed potato, strawberry, pineapple, papaya etc. Even in seed-grown plants, this technology has application in overcoming the barriers like dormancy, sexual compatibility, germination etc. But the major drawback of tissue culture raised plantlets is that they show somaclonal variation, i.e. alteration in the genetic constitution of the plant leading to the disappearance of true-to-type nature and resulting variants may not be desirable.? In such case, the genetic fidelity test is mandatory to confirm the true-to-type genetic makeup of newly derived plantlets. Several strategies have been used to ascertain the genetic fidelity of the in vitro raised progenies comprising morpho-physiological, biochemical and cytological approaches. These approaches are mainly based on phenotypic characters, which can be affected by the in-vitro manipulation, environment and types of plant tissue; hence it is not easy to differentiate clonal fidelity with a high probability. In contrast, for a similar purpose, the DNA- based molecular markers are versatile tools with broader applicability in various fields of applied biology. These molecular markers have the edge over aforementioned traditional non-DNA based markers concerning environmental interaction, developmental stage, tissue, time and cost. The present paper contains different techniques of genetic fidelity assay to confirm the true-to-type genetic constitution in tissue culture raised crops.
机译:组织培养技术被广泛用于在较短的时间和空间范围内在人工培养基上无菌生产大规模无病的种植材料。近年来,这项技术已广泛用于商业化生产多种克隆繁殖的植物,例如香蕉,竹子,尖尖的护枝,种薯,草莓,菠萝,木瓜等。即使在种子种植的植物中,该技术也可用于克服但是,组织培养引起的幼苗的主要缺点是它们表现出体细胞克隆变异,即植物的遗传组成发生改变,导致真实型自然和所导致的变异消失可能不是理想的。在这种情况下,必须进行遗传保真度测试以确认新近衍生的小植株的真实类型的基因组成。已经使用了几种策略来确定体外产生的后代的遗传保真度,包括形态生理,生化和细胞学方法。这些方法主要基于表型特征,这些特征可能会受到体外操作,环境和植物组织类型的影响。因此,很难轻易地区分出克隆保真度。相反,出于相似的目的,基于DNA的分子标记是用途广泛的工具,在应用生物学的各个领域具有更广泛的适用性。这些分子标记在环境相互作用,发育阶段,组织,时间和成本方面比上述传统的基于非DNA的标记具有优势。本文包含不同的遗传保真度分析技术,以确认组织培养的农作物中的真实型遗传组成。

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