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| Status |
Public on Nov 30, 2015 |
| Title |
Comparative genomic analyses of the human NPHP1 locus reveal complex genomic architecture and its regional evolution in primates |
| Platform organism |
Homo sapiens |
| Sample organisms |
Macaca mulatta; Papio anubis; Gorilla gorilla; Pan troglodytes; Pongo abelii; Homo sapiens |
| Experiment type |
Genome variation profiling by genome tiling array
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| Summary |
Many loci in the human genome harbor complex genomic structures that can result in susceptibility to genomic rearrangements leading to various genomic disorders. Nephronophthisis 1 (NPHP1, MIM# 256100) is an autosomal recessive disorder that can be caused by defects of NPHP1; the gene maps within the human 2q13 region where low copy repeats (LCRs) are abundant. Loss of function of NPHP1 is responsible for approximately 85% of the NPHP1 cases - about 80% of such individuals carry a large recurrent homozygous NPHP1 deletion that occurs via non-allelic homologous recombination (NAHR) between two flanking directly oriented ~45 kb LCRs. Published data revealed a non-pathogenic inversion polymorphism involving the NPHP1 gene flanked by two inverted ~358 kb LCRs. Using optical mapping and array-comparative genomic hybridization, we identified three potential novel structural variant (SV) haplotypes at the NPHP1 locus that may protect a haploid genome from genomic instability and NPHP1 deletion. Inter-species comparative genomic analyses among primate genomes revealed massive genomic changes during evolution. The aggregated data suggest that dynamic genomic rearrangements occurred historically within the NPHP1 locus and generated SV haplotypes observed in the human population today, which may have differential susceptibility to the NPHP1 deletion within a personal genome. Our study documents diverse SV haplotypes at a complex LCR-laden human genomic region. Comparative analyses provide a model for how this complex region arose during primate evolution, and studies among humans reflect the possibility that intra-species polymorphism may potentially modulate an individual’s susceptibility to acquiring disease-associated alleles.
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| Overall design |
aCGH experiments were performed on DNA samples from human subjects without NPHP1 (N=10), DNA samples from human subjects affected with NPHP1 (N=8), and nonhuman primate DNA samples of baboon (N=1), rhesus macaque (N=2), orangutan (N=1), gorilla (N=3) and chimpanzee (N=7). Human DNA sample of NA10851 were used as the universal reference for the aCGH experiment.
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| Contributor(s) |
Yuan B, Lupski JR |
| Citation(s) |
26641089 |
| |
| Submission date |
Oct 13, 2015 |
| Last update date |
Feb 18, 2016 |
| Contact name |
Bo Yuan |
| E-mail(s) |
yuanbo1007@gmail.com
|
| Organization name |
Baylor College of Medicine
|
| Street address |
One Baylor Plaza
|
| City |
Houston |
| ZIP/Postal code |
77030 |
| Country |
USA |
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| Platforms (1) |
| GPL21019 |
Agilent-032837 Homo sapiens 2q13_Pengfei |
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| Samples (32)
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| Relations |
| BioProject |
PRJNA298584 |
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