Franck P, Garnery L, Loiseau A, Oldroyd B P, Hepburn H R, Solignac M, Cornuet J M
Centre de Biologie et de Gestion des Populations, Campus International de Baillarguet, 34980 Monferrier-sur-Lez, France.
Heredity (Edinb). 2001 Apr;86(Pt 4):420-30. doi: 10.1046/j.1365-2540.2001.00842.x.
A total of 738 colonies from 64 localities along the African continent have been analysed using the DraI RFLP of the COI-COII mitochondrial region. Mitochondrial DNA of African honeybees appears to be composed of three highly divergent lineages. The African lineage previously reported (named A) is present in almost all the localities except those from north-eastern Africa. In this area, two newly described lineages (called O and Y), putatively originating from the Near East, are observed in high proportion. This suggests an important differentiation of Ethiopian and Egyptian honeybees from those of other African areas. The A lineage is also present in high proportion in populations from the Iberian Peninsula and Sicily. Furthermore, eight populations from Morocco, Guinea, Malawi and South Africa have been assayed with six microsatellite loci and compared to a set of eight additional populations from Europe and the Middle East. The African populations display higher genetic variability than European populations at all microsatellite loci studied thus far. This suggests that African populations have larger effective sizes than European ones. According to their microsatellite allele frequencies, the eight African populations cluster together, but are divided in two subgroups. These are the populations from Morocco and those from the other African countries. The populations from southern Europe show very low levels of 'Africanization' at nuclear microsatellite loci. Because nuclear and mitochondrial DNA often display discordant patterns of differentiation in the honeybee, the use of both kinds of markers is preferable when assessing the phylogeography of Apis mellifera and to determine the taxonomic status of the subspecies.
利用细胞色素氧化酶亚基I-细胞色素氧化酶亚基II(COI-COII)线粒体区域的DraI限制性片段长度多态性(RFLP),对来自非洲大陆64个地区的总共738个蜂群进行了分析。非洲蜜蜂的线粒体DNA似乎由三个高度分化的谱系组成。先前报道的非洲谱系(命名为A)几乎存在于所有地区,但非洲东北部的地区除外。在该地区,观察到两个新描述的谱系(称为O和Y),推测起源于近东地区,且比例很高。这表明埃塞俄比亚和埃及的蜜蜂与非洲其他地区的蜜蜂存在重要差异。A谱系在伊比利亚半岛和西西里岛的种群中也占很高比例。此外,对来自摩洛哥、几内亚、马拉维和南非的8个种群进行了6个微卫星位点的检测,并与另外一组来自欧洲和中东的8个种群进行了比较。在目前研究的所有微卫星位点上,非洲种群显示出比欧洲种群更高的遗传变异性。这表明非洲种群的有效种群大小比欧洲种群更大。根据微卫星等位基因频率,这8个非洲种群聚在一起,但分为两个亚组。它们是来自摩洛哥的种群和来自其他非洲国家的种群。南欧种群在核微卫星位点上显示出非常低水平的“非洲化”。由于在蜜蜂中核DNA和线粒体DNA常常表现出不一致的分化模式,因此在评估西方蜜蜂的系统地理学和确定亚种的分类地位时,同时使用这两种标记更为可取。