Multiple sclerosis (MS) is a debilitating neuroimmunological and neuro-degenerative disease. Despite substantial evidence for polygenic inheritance, the MHC is the only region that clearly and consistently demonstrates linkage and association in MS studies. The goal of the work presented in this dissertation was to identify additional chromosomal regions harboring MS susceptibility genes. Our studies entailed a new genomic convergence approach incorporating information gained from positional (linkage and association) and functional (comparative sequence) studies. In conjunction with high-throughput genotyping and powerful new statistical analyses methods, this approach identified several regions suggesting the presence of MS loci.
We began our investigation with a genomic linkage screen that identified seven chromosomal regions of interest in a data set of multiplex MS families. To narrow these regions, we developed an approach for more detailed linkage studies that capitalized on new methods for rapid and accurate genotyping of SNPs. In addition to increasing marker coverage in each region, we genotyped an expanded data set and devised covariate analyses schemes to account for genetic effect in the MHC. This method
continued to provide evidence of linkage to several chromosomal regions and was successful in substantially narrowing two regions to only a few Mb.
We then developed a systematic approach to expedite follow-up association studies in the positional candidate regions. In an attempt to increase the likelihood of detecting variants associated with MS, we employed a novel method to select SNPs located in multi-species conserved sequences. Use of this method on chromosome 1q44 resulted in the identification of four subregions demonstrating significant association with MS susceptibility.
The work presented in this dissertation confirmed several regions warranting further investigation for genes conferring susceptibility to MS, including chromosomes 1q44, 2q35, 9q34, and 18p11. It is our hope that these studies will result in the discovery of several genes associated with MS and that our genomic convergence approach will provide researchers with a method for unraveling the genetic heterogeneity of MS and other complex genetic diseases.
| Identifer | oai:union.ndltd.org:VANDERBILT/oai:VANDERBILTETD:etd-04042006-040044 |
| Date | 18 April 2006 |
| Creators | Kenealy, Shannon |
| Contributors | Professor Jonathan L. Haines, Professor Douglas P. Mortlock, Professor John A. Phillips, Professor Subramaniam Sriram, Professor Marshall L. Summar, Professor Scott M. Williams |
| Publisher | VANDERBILT |
| Source Sets | Vanderbilt University Theses |
| Language | English |
| Detected Language | English |
| Type | text |
| Format | application/pdf |
| Source | http://etd.library.vanderbilt.edu/available/etd-04042006-040044/ |
| Rights | unrestricted, I hereby certify that, if appropriate, I have obtained and attached hereto a written permission statement from the owner(s) of each third party copyrighted matter to be included in my thesis, dissertation, or project report, allowing distribution as specified below. I certify that the version I submitted is the same as that approved by my advisory committee. I hereby grant to Vanderbilt University or its agents the non-exclusive license to archive and make accessible, under the conditions specified below, my thesis, dissertation, or project report in whole or in part in all forms of media, now or hereafter known. I retain all other ownership rights to the copyright of the thesis, dissertation or project report. I also retain the right to use in future works (such as articles or books) all or part of this thesis, dissertation, or project report. |
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