Morelli L, Grosso M G, Vona G, Varesi L, Torroni A, Francalacci P
Dipartimento di Zoologia e Antropologia Biologica, Università di Sassari, Italy.
Hum Biol. 2000 Aug;72(4):585-95.
Mitochondrial DNA (mtDNA) polymorphisms were analyzed by polymerase chain reaction amplification and haplogroup-specific restriction screening in populations from Corsica and Sardinia. These included 56 individuals from the area of Corte, central Corsica (France), 51 individuals from Gallura, northern Sardinia (Italy), and 45 individuals from Barbagia, central Sardinia. The screening revealed that about 95% of mtDNAs could be grouped in 8 of the 9 European haplogroups, including H-K, T-V, and X. Our results confirmed that these haplogroups encompass virtually all the mitochondrial lineages present in Europe and can be detected in both northern and southern European populations. We also discovered 2 restriction sites (-73 Alw441 and +75 SphI) that allow the detection of informative nucleotide changes in the second hypervariable segment of the control region, which help to detect the haplogroup identity of mtDNAs without requiring further DNA sequencing. Haplogroup H was the most common mtDNA lineage in this sample, reaching frequencies from about 40% in Corsican and Gallurese populations, to about 65% in the Barbagian population. Haplogroup V, possibly originating in the Iberian peninsula, was found only in the central Sardinian sample. Of the 5 Corsican mtDNAs belonging to the haplogroup T, 4 had a restriction fragment length polymorphism found only in this population. It seems that this mutation originated in Corsica and has had time to spread in the area, since the maternal grandmothers of the subjects came from different villages of the island. The sample from central Sardinia shows a remarkable discontinuity with those from the northern part of the island and from Corsica. Gallura and Corsica seem to have undergone a more recent peopling event, possibly related to the arrival of new mitochondrial variability from continental Italy, while Barbagia has apparently maintained more archaic haplotypes.
通过聚合酶链反应扩增和单倍群特异性限制性筛选,对来自科西嘉岛和撒丁岛人群的线粒体DNA(mtDNA)多态性进行了分析。这些人群包括来自法国科西嘉岛中部科尔特地区的56人、来自意大利撒丁岛北部加卢拉的51人以及来自撒丁岛中部巴尔巴吉亚的45人。筛选结果显示,约95%的mtDNA可归为9个欧洲单倍群中的8个,包括H-K、T-V和X。我们的结果证实,这些单倍群几乎涵盖了欧洲所有的线粒体谱系,在北欧和南欧人群中均能检测到。我们还发现了2个限制性位点(-73 Alw441和+75 SphI),可用于检测控制区第二高变区中信息丰富的核苷酸变化,这有助于在无需进一步DNA测序的情况下检测mtDNA的单倍群身份。单倍群H是该样本中最常见的mtDNA谱系,在科西嘉人和加卢拉人群中的频率约为40%,在巴尔巴吉亚人群中约为65%。单倍群V可能起源于伊比利亚半岛,仅在撒丁岛中部样本中被发现。在属于单倍群T的5个科西嘉mtDNA中,有4个具有仅在该人群中发现的限制性片段长度多态性。这种突变似乎起源于科西嘉岛,并且有时间在该地区传播,因为受试者的外祖母来自该岛的不同村庄。撒丁岛中部的样本与该岛北部和科西嘉岛的样本存在显著差异。加卢拉和科西嘉似乎经历了更近的人口迁移事件,可能与来自意大利大陆的新线粒体变异的到来有关,而巴尔巴吉亚显然保留了更多古老的单倍型。