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通过分子标记评估香草(香荚兰安德鲁斯)长期微繁殖茎尖培养物的遗传保真度。

Genetic fidelity of long-term micropropagated shoot cultures of vanilla (Vanilla planifolia Andrews) as assessed by molecular markers.

作者信息

Sreedhar Reddampalli V, Venkatachalam Lakshmanan, Bhagyalakshmi Neelwarne

机构信息

Plant Cell Biotechnology Department, Central Food Technological Research Institute, Mysore, India.

出版信息

Biotechnol J. 2007 Aug;2(8):1007-13. doi: 10.1002/biot.200600229.

Abstract

Occurrence of genetic variants during micropropagation is occasionally encountered when the cultures are maintained in vitro for long period. Therefore, the micropropagated multiple shoots of Vanilla planifolia Andrews developed from axillary bud explants established 10 years ago were used to determine somaclonal variation using random amplified polymorphic DNA (RAPD) and intersimple sequence repeats markers (ISSR). One thousand micro-plants were established in soil of which 95 plantlets (consisting of four phenotypes) along with the mother plant were subjected to genetic analyses using RAPD and ISSR markers. Out of the 45 RAPD and 20 ISSR primers screened, 30 RAPD and 7 ISSR primers showed 317 clear, distinct and reproducible band classes resulting in a total of 30 115 bands. However, no difference was observed in banding patterns of any of the samples for a particular primer, indicating the absence of variation among the micropropagated plants. Our results allow us to conclude that the micropropagation protocol that we have used for in vitro proliferation of vanilla plantlets for the last 10 years might be applicable for the production of clonal plants over a considerable period of time.

摘要

当培养物在体外长期保存时,微繁殖过程中偶尔会出现遗传变异。因此,利用随机扩增多态性DNA(RAPD)和简单序列重复区间标记(ISSR),对10年前建立的从腋芽外植体发育而来的香荚兰微繁殖多芽进行体细胞克隆变异检测。将1000株微型植株移栽到土壤中,其中95株(包含4种表型)连同母株一起,使用RAPD和ISSR标记进行遗传分析。在筛选的45个RAPD引物和20个ISSR引物中,30个RAPD引物和7个ISSR引物显示出317个清晰、独特且可重复的条带类别,总共产生30115条带。然而,对于特定引物,任何样品的条带模式均未观察到差异,表明微繁殖植株之间不存在变异。我们的结果使我们能够得出结论,在过去10年中我们用于香荚兰微型植株体外增殖的微繁殖方案可能在相当长的一段时间内适用于克隆植物的生产。

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