Analysis of the multi-copy gene family FAM90A as a copy number variant in different ethnic backgrounds

被引:3
|
作者
Bosch, Nina [1 ,2 ]
Escaramis, Georgia [1 ,2 ]
Mercader, Josep M. [1 ,2 ]
Armengol, Lluis [1 ,2 ]
Estivill, Xavier [1 ,2 ,3 ]
机构
[1] CRG UPF, Genes & Dis Programme, Genet Causes Dis Grp, Barcelona 08003, Catalonia, Spain
[2] CIBERESP, Barcelona, Catalonia, Spain
[3] Pompeu Fabra Univ, Dept Hlth & Expt Life Sci, Barcelona, Catalonia, Spain
关键词
FAM90A (family with sequence similarity 90; GenBank; NM_018088); inter-population variability; real-time PCR;
D O I
10.1016/j.gene.2008.05.003
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Copy number variants contribute extensively to inter-individual genomic differences, but little is known about their inter-population variability and diversity. In a previous study (Bosch et al., 2007: 16:2572-2582). we reported that the primate-specific gene family FAM90A, which accounts for as many as 25 members in the human reference assembly, has expanded the number of FAM90A clusters across the hominoid lineage. Here we examined the copy number variability of FAM90A genes in 260 HapMap samples of European, African, and Asian ancestry, and showed significant inter-population differences (p < 0.0001). Based on the recent study of Stranger et al. (2007; 315:848-853), we also explored the correlation between copy number variability and expression levels of the FAM90A gene family. Despite the high genomic variability, we found a low correlation between FAM90A copy number and expression levels, which could be due to the action of independent trans-acting factors. Our results show that FAM90A is highly variable in copy number between individuals and between populations. However, this variability has little impact on gene expression levels, thus highlighting the importance of genomic variability for genes located in regions containing segmental duplications. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:113 / 117
页数:5
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