Vandewoestijne S, Baguette M
Unité d'Ecologie et de Biogéographie, Université catholique de Louvain, Place Croix du Sud 4-5, B-1348 Louvain-la-Neuve, Belgium.
Heredity (Edinb). 2002 Dec;89(6):439-45. doi: 10.1038/sj.hdy.6800161.
The genetic population structure of the Cranberry Fritillary Boloria aquilonaris was studied using both RAPDs (random amplified polymorphic DNA) and allozymes. In Belgium, B. aquilonaris has a naturally fragmented distribution that has been accentuated due to human activity during the last century. The genetic population structure of this butterfly was analysed at the regional (several Ardenne uplands) and at the landscape level (several populations within an Ardenne upland). Both population genetic markers confirmed results from a previous CMR study at the landscape scale. At the regional scale however, important incongruences were observed between RAPDs and allozymes. The average gene diversity for the RAPD data was twice that of the allozyme data. The degree of population subdivision was also much greater for RAPDs than for allozymes. The UPGMA clusters produced by each of these markers differed significantly. We believe that, given the higher rate of mutation of RAPDs and the greater number of loci assayed by this method, RAPDs reveal a more accurate and recent population genetic structure than allozymes.
利用随机扩增多态性DNA(RAPD)和等位酶对越橘豹蛱蝶(Boloria aquilonaris)的遗传种群结构进行了研究。在比利时,越橘豹蛱蝶具有自然碎片化的分布,且在上个世纪由于人类活动这种分布碎片化情况加剧。在区域层面(几个阿登高地)和景观层面(一个阿登高地内的几个种群)分析了这种蝴蝶的遗传种群结构。两种种群遗传标记都证实了之前在景观尺度上进行的CMR研究结果。然而,在区域尺度上,观察到RAPD和等位酶之间存在重要的不一致。RAPD数据的平均基因多样性是等位酶数据的两倍。RAPD的种群细分程度也比等位酶大得多。由这些标记各自产生的UPGMA聚类有显著差异。我们认为,鉴于RAPD的突变率更高以及该方法检测的基因座数量更多,与等位酶相比,RAPD揭示了更准确和更新的种群遗传结构。