RAPD-PCR、基因特异性ITS和rbcl标记揭示西番莲物种的进化趋势

Bipin D. Lade, Anita S. Patil
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摘要

背景:本研究通过对西番莲属植物ITS和rbcL特异序列的扩增基因型数据和非特异RAPD-PCR标记进行分子系统发育研究,初步分析了西番莲属植物的遗传多样性。方法:PCR-RAPD采用10条多态DNA引物,在NTSYS软件上编译构建树状图。基因特异性ITS和rbcL引物用于基因组特异性扩增。扩增的ITS和rbcL标记采用最大简约(MP)和最大似然(ML)方法组装。利用BLAST、CLUSTAL W和MEGA 6.0软件进行最终的亲缘关系树分析。结果:PCR-RAPD引物可翻译133个随机扩增的多态性DNA。NTSYS树形图将来自印度那格浦尔Ramdaspeth和Shankar Nagar Nagar的P. vitifolia放在同一枝上(相似系数0.609),证实来自印度那格浦尔。此外,来自英格兰的foetida与印度的foetida在地理上表现出种内变异,并不是同一进化支。此外,还观察了构建树的变化与系统发育方法MS/ML的变化。ITS MP共识树由强100引导值支持,P. vitifolia (HNI和RNI)和P. foetida (UAI和UGI)在相同的进化枝上聚类。然而,在MP和ML方法中,rbcL尚未恢复到单一种。因此,rbcL具有区分西番莲属植物的倾向,不允许在同一枝的同一种周围聚集,并且ITS区域具有简约信息位点,可以在种间水平上提供有效的分辨率和识别。结论:RAPD的性能评价显示100%的PCR成功率,有时扩增率较低。ITS区在种间鉴定上效果最好,而rbcL区在种间鉴定上效果最好,可以作为西番莲种间系统发育群落的局部DNA条形码。
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Evolutionary Trend in Passiflora Species Revealed by RAPD-PCR, Gene Specific ITS and rbcl Markers
Background: The present study represents a preliminary analysis of genetic diversity among Passiflora species using amplified genotypic data of specific ITS and rbcL sequences and non-specific RAPD-PCR markers for investigation of the molecular phylogeny. Methods: The PCR-RAPD uses ten primers for polymorphic DNA, which are compiled on NTSYS software to construct dendrogram.  The gene specific ITS and rbcL primers are used for specific amplification from genomic. The amplified ITS and rbcL markers assembled using Maximum Parsimony (MP) and Maximum likelihood (ML) methods. The BLAST, CLUSTAL W, and MEGA 6.0 have been used to conclude final genetic relation tree. Results: The PCR-RAPD primers translate 133 random amplified polymorphic DNA. NTSYS dendrogram placed P. vitifolia from Ramdaspeth and Shankar Nagar Nagpur, India in same clade (similarity coefficient 0.609) confirming same origin  Nagpur India. Moreover, P. foetida from England is not coming in same clade with Indian P. foetida showing geographically intra-specific variation. In addition, the change in a constructed tree was observed with respect to change in phylogeny methods MS/ML. The ITS MP consensus tree is supported by strong 100 bootstrap value, clusters P. vitifolia (HNI and RNI) and P. foetida (UAI and UGI) in equivalent clade. However, no single species have been recovered using rbcL in MP and ML method. Thus, it is inference that rbcL have tendency to differentiate Passiflora species not allowing clustering around same species in same clade and the ITS region having parsimony informative sites that provide valid resolution and identification at inter-intra species level. Conclusions: The evaluation of properties of RAPD indicates 100% PCR success, sometimes with low rate of amplification. The ITS region found to be best for identification at inter-intra species, On the contrary, rbcL region is good to distinguished inter species, making it best as local DNA barcode for marking a Passiflora species in phylogenetic community.
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