Lao Oscar, Andrés Aida M, Mateu Eva, Bertranpetit Jaume, Calafell Francesc
Unitat de Biologia Evolutiva, Facultat de Ciències de la Salut i de la Vida, Universitat Pompeu Fabra, Barcelona, Catalonia, Spain.
Eur J Hum Genet. 2003 May;11(5):385-94. doi: 10.1038/sj.ejhg.5200970.
Cystic fibrosis (CF) is the most frequent severe recessive disorder in European populations. We have analyzed its mutation frequency spectrum in 94 European, North African and SW Asian populations taken from the literature. Most major mutations as well as the incidence of CF mutations showed clinals patterns as demonstrated by autocorrelogram analysis. More importantly, measures of mutation diversity did also show clinal patterns, with mutation spectra being more diverse in southern than in northern Europe. This increased diversity would imply roughly a three-fold long-term effective population size in southern than in northern Europe. Distances were computed among populations based on their CF mutation frequencies and compared with distances based on other genic regions. CF-based distances correlated with mtDNA but not with Y-chromosome-based distances, which may be a consequence of the relatively homogeneous CF mutation frequencies in European populations.
囊性纤维化(CF)是欧洲人群中最常见的严重隐性疾病。我们分析了从文献中获取的94个欧洲、北非和西南亚人群的突变频率谱。如自相关图分析所示,大多数主要突变以及CF突变的发生率呈现出临床模式。更重要的是,突变多样性的测量也显示出临床模式,即北欧的突变谱比南欧的突变谱更加多样化。这种增加的多样性意味着南欧的长期有效种群规模大约是北欧的三倍。根据人群的CF突变频率计算了它们之间的距离,并与基于其他基因区域的距离进行了比较。基于CF的距离与线粒体DNA(mtDNA)相关,但与基于Y染色体的距离不相关,这可能是欧洲人群中CF突变频率相对均匀的结果。