用DNA指纹分析监测马铃薯组织培养微块茎病毒

Khalid A. El-Doug, A. Reh, A. Saba, M. Hazza, A. Kandeel
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引用次数: 1

摘要

采用简单的ISSR-PCR方法检测马铃薯微块茎PVY衍生苗的体细胞无性系变异,为快速批量繁殖过程中质量控制的精确监测奠定了基础。有效管理微块茎遗传资源。本研究报道了利用ISSR-PCR检测马铃薯微繁植株遗传变异的方法。利用ISSR-DNA标记对马铃薯微块茎进行筛选。选择3个ISSR引物在离体培养中产生多态dna片段,用于分化所研究的植株和微块茎。dna指纹图谱显示了遗传变异,治疗苗有40%的多态性,分析的马铃薯苗约有50%,每个引物有4.5个多态性片段。从茉莉酸和香豆素制备的微块茎中分离到dna片段,经ISSR扩增,发现微块茎的片段谱明显相同。体细胞无性系变异的频率被发现是病毒治疗和微结核诱导剂。只有在高茉莉素和香豆素浓度下才检测到体细胞无性系变异。虽然在一些无性系的微块茎中记录了微小的形态变化。不同的微繁殖无性系发育的片段特征与供体母株具有一定的相似性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Monitoring of Microtubers Virus Tested-Derived Potato Tissue Culture by DNA Fingerprint Analysis
A simple ISSR-PCR as a routine method of microtuber PVY tested derived potato plantlets for somaclonal variations is aperquist for pricise monitoring of quality control during rapid mass micropropagation. and effective management of microtubers genetic resoures. This study reports on the use of ISSR-PCR for detection of genetic variations in micripropagated potato plants. Microtubers PVY testedderived potato plantlets were screened using ISSR-DNA markers. Three ISSR primers were chosen as producing polymorphic D N A fragments differentiating the investigated plantlets and microtubers in vitro. D N A fingerprint revealed genetic variations, 4 0 % polymorphisms of therapeutic plantlets, approximately 5 0 % of the analyzed potato plantlets with 4.5 polymorphic fragments per primer. While the D N A was isolated from microtubers produced using jasmonic acid and coumarin after ISSR amplification it was obvious that microtuber identical fragments profile. The frequency of somaclonal variations was found to be virus therapeutic and microtuberization inducers. The somaclonal variations were only detected in high jasmonic and coumarin concentrations. Although minor morphological variations were recorded in the microtubers of some clones. The developed fragments profiles of different micropropagated clones were typical to that of the donor mother plants.
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