High-Resolution Copy-Number Variation Map Reflects Human Olfactory Receptor Diversity and Evolution

被引:80
|
作者
Hasin, Yehudit [1 ]
Olender, Tsviya [1 ]
Khen, Miriam [1 ]
Gonzaga-Jauregui, Claudia [1 ,2 ]
Kim, Philip M. [3 ]
Urban, Alexander Eckehart [4 ]
Snyder, Michael [3 ,4 ]
Gerstein, Mark B. [3 ,5 ,6 ]
Lancet, Doron [1 ]
Korbel, Jan O. [3 ,7 ]
机构
[1] Weizmann Inst Sci, Dept Mol Genet, IL-76100 Rehovot, Israel
[2] Univ Nacl Autonoma Mexico, Ctr Ciencias Genom, Cuernavaca 62191, Morelos, Mexico
[3] Yale Univ, Dept Mol Biophys & Biochem, New Haven, CT USA
[4] Yale Univ, Dept Mol Cellular & Dev Biol, New Haven, CT USA
[5] Yale Univ, Program Computat Biol & Bioinformat, New Haven, CT USA
[6] Yale Univ, Dept Comp Sci, New Haven, CT 06520 USA
[7] European Mol Biol Lab, Struct & Computat Biol Unit, Heidelberg, Germany
来源
PLOS GENETICS | 2008年 / 4卷 / 11期
关键词
D O I
10.1371/journal.pgen.1000249
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Olfactory receptors (ORs), which are involved in odorant recognition, form the largest mammalian protein superfamily. The genomic content of OR genes is considerably reduced in humans, as reflected by the relatively small repertoire size and the high fraction (similar to 55%) of human pseudogenes. Since several recent low-resolution surveys suggested that OR genomic loci are frequently affected by copy-number variants (CNVs), we hypothesized that CNVs may play an important role in the evolution of the human olfactory repertoire. We used high-resolution oligonucleotide tiling microarrays to detect CNVs across 851 OR gene and pseudogene loci. Examining genomic DNA from 25 individuals with ancestry from three populations, we identified 93 OR gene loci and 151 pseudogene loci affected by CNVs, generating a mosaic of OR dosages across persons. Our data suggest that similar to 50% of the CNVs involve more than one OR, with the largest CNV spanning 11 loci. In contrast to earlier reports, we observe that CNVs are more frequent among OR pseudogenes than among intact genes, presumably due to both selective constraints and CNV formation biases. Furthermore, our results show an enrichment of CNVs among ORs with a close human paralog or lacking a one-to-one ortholog in chimpanzee. Interestingly, among the latter we observed an enrichment in CNV losses over gains, a finding potentially related to the known diminution of the human OR repertoire. Quantitative PCR experiments performed for 122 sampled ORs agreed well with the microarray results and uncovered 23 additional CNVs. Importantly, these experiments allowed us to uncover nine common deletion alleles that affect 15 OR genes and five pseudogenes. Comparison to the chimpanzee reference genome revealed that all of the deletion alleles are human derived, therefore indicating a profound effect of human-specific deletions on the individual OR gene content. Furthermore, these deletion alleles may be used in future genetic association studies of olfactory inter-individual differences.
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页数:14
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