Cutler Gene, Marshall Lisa A, Chin Ni, Baribault Helene, Kassner Paul D
Lead Discovery, Amgen, South San Francisco, California 94080, USA.
Genome Res. 2007 Dec;17(12):1743-54. doi: 10.1101/gr.6754607. Epub 2007 Nov 7.
The contribution to genetic diversity of genomic segmental copy number variations (CNVs) is less well understood than that of single-nucleotide polymorphisms (SNPs). While less frequent than SNPs, CNVs have greater potential to affect phenotype. In this study, we have performed the most comprehensive survey to date of CNVs in mice, analyzing the genomes of 42 Mouse Phenome Consortium priority strains. This microarray comparative genomic hybridization (CGH)-based analysis has identified 2094 putative CNVs, with an average of 10 Mb of DNA in 51 CNVs when individual mouse strains were compared to the reference strain C57BL/6J. This amount of variation results in gene content that can differ by hundreds of genes between strains. These genes include members of large families such as the major histocompatibility and pheromone receptor genes, but there are also many singleton genes including genes with expected phenotypic consequences from their deletion or amplification. Using a whole-genome association analysis, we demonstrate that complex multigenic phenotypes, such as food intake, can be associated with specific copy number changes.
与单核苷酸多态性(SNP)相比,基因组片段拷贝数变异(CNV)对遗传多样性的贡献还不太为人所了解。虽然CNV的发生频率低于SNP,但它们影响表型的潜力更大。在本研究中,我们对小鼠的CNV进行了迄今为止最全面的调查,分析了42个小鼠表型组联盟重点品系的基因组。这种基于微阵列比较基因组杂交(CGH)的分析鉴定出了2094个推定的CNV,当将各个小鼠品系与参考品系C57BL/6J进行比较时,在51个CNV中平均有10 Mb的DNA。这种变异量导致不同品系之间的基因含量可能相差数百个基因。这些基因包括大家族的成员,如主要组织相容性和信息素受体基因,但也有许多单拷贝基因,包括那些因缺失或扩增而具有预期表型后果的基因。使用全基因组关联分析,我们证明复杂的多基因表型,如食物摄入量,可能与特定的拷贝数变化有关。