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Genome-wide linkage analysis of a Parkinsonian-pyramidal syndrome pedigree by 500 K SNP arrays |
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| Authors: | Shojaee Seyedmehdi Sina Farzad Banihosseini Setareh Sadat Kazemi Mohammad Hossein Kalhor Reza Shahidi Gholam-Ali Fakhrai-Rad Hossein Ronaghi Mostafa Elahi Elahe |
| Affiliation: | 1 Department of Biotechnology, College of Science, University of Tehran, Tehran, Iran 2 School of Biology, College of Science, University of Tehran, Tehran, Iran 3 Center of Excellence in Biomathematics, School of Mathematics, Statistics and Computer Science, College of Science, University of Tehran, Tehran, Iran 4 Iran University of Medical Sciences, Hazrat Rasool Hospital, Tehran, Iran 5 Tehran University of Medical Sciences, Tehran, Iran 6 Molecular and Computational Biology, Department of Biological Sciences, University of Southern California, Los Angeles, CA 90089, USA 7 Stanford Genome Technology Center, Stanford University, Palo Alto, CA 94304, USA |
| Abstract: | Robust SNP genotyping technologies and data analysis programs have encouraged researchers in recent years to use SNPs for linkage studies. Platforms used to date have been 10 K chip arrays, but the possible value of interrogating SNPs at higher densities has been considered. Here, we present a genome-wide linkage analysis by means of a 500 K SNP platform. The analysis was done on a large pedigree affected with Parkinsonian-pyramidal syndrome (PPS), and the results showed linkage to chromosome 22. Sequencing of candidate genes revealed a disease-associated homozygous variation (R378G) in FBXO7. FBXO7 codes for a member of the F-box family of proteins, all of which may have a role in the ubiquitin-proteosome protein-degradation pathway. This pathway has been implicated in various neurodegenerative diseases, and identification of FBXO7 as the causative gene of PPS is expected to shed new light on its role. The performance of the array was assessed and systematic analysis of effects of SNP density reduction was performed with the real experimental data. Our results suggest that linkage in our pedigree may have been missed had we used chips containing less than 100,000 SNPs across the genome. |
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