Genes research

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Genes research

Postby bromley » Mon Sep 25, 2006 9:53 am

International team analyses human genetic variation in key immune region

In-depth analysis will enable scientists to identify genetic risk factors for common immune diseases.

An international group of researchers today unveiled a detailed map of human genetic variation within the major histocompatibility complex (MHC), the most important region of the human genome encoding the human response to infection, autoimmune disease and organ transplantation. The work represents a milestone in the analysis of genetic variability for this fundamental immune region and lays the scientific foundation for future efforts aimed at uncovering the genetic roots of immune-related diseases. The findings of this international team, which includes scientists from the Montreal Heart Institute (MHI), the Université de Montréal (UdeM), the Broad Institute of MIT and Harvard and several other research institutions, appear in the September 24 advance online edition of Nature Genetics.

"This new map will be a key resource for researchers to use to find genes affecting health, disease, and responses to medications," said senior author Dr. John D. Rioux, PhD, who is associate professor of medicine at the UdeM and at the MHI where he works as a researcher and director of the Laboratory in Genetics and Genomic Medicine of Inflammation, visiting scientist of the Broad Institute of MIT and Harvard, and holder of the Canada Research Chair in Genetics and Genomic Medicine of Inflammation. "It will provide the information necessary to design powerful studies to identify the genetic risk factors located within the MHC."

The MHC -- specifically, the genes that comprise it -- is associated with more diseases than any other region of the human genome. This includes common diseases such as atherosclerosis, arthritis, diabetes, HIV, lupus, multiple sclerosis and Crohn's disease. However, pinpointing the specific changes that are causative in these diseases has been complicated by two factors: the extremely high degree of genetic diversity that exists in the MHC among different individuals and the tendency for multiple genetic differences in this region to be inherited together in groups called "haplotypes."

To characterise the haplotype patterns of the MHC, the researchers analysed the variability in its DNA sequence in more than 350 individuals from diverse geographic regions, including Africa, Europe, China and Japan. Specifically, the researchers "read" ~7,500 single-letter changes in the genetic code called single nucleotide polymorphisms (SNPs) together with short segments of DNA sequence from a set of highly variable genes within the MHC, called "HLA genes." These genes form a distinctive fingerprint that is recognised by an individual's immune system to distinguish foreign tissues from "self" tissues and the genes' DNA sequences are frequently analysed (a process called "HLA typing") in patients who receive organ transplants or suffer from autoimmune disease.

Importantly, the researchers' data and analyses, which are made available online to the entire scientific community, provide the tools needed to begin the initial efforts toward identifying genetic risk factors in the MHC for common immune-mediated diseases. Such endeavors, involving researchers at the Montreal Heart Institute, the University of California, San Francisco and the Broad Institute of MIT and Harvard, are now underway for several immune system diseases.

In addition, the results offer insights into the evolutionary history of the MHC region -- its early origins and the evolutionary forces that have helped to shape it over time. The findings also suggest that analysing select SNPs within the HLA genes may offer a more economical alternative for characterising the most common genetic variants in the region than standard HLA typing methods.

Nearly three-quarters of the DNA samples that the scientists analysed had been previously examined as part of the International Haplotype Map ("HapMap") Project, a worldwide scientific collaboration to catalogue human genetic variation on a genome-wide scale. The latest findings, particularly the analyses of the HLA gene region, provide new and complementary information that can be integrated with data from the recently completed HapMap Project as well as other genomic efforts, to provide a comprehensive view of genetic variability in the human MHC.

Data access

Data from the project will be made publicly available at the following website:

de Bakker P.I.W. et al. (2006) A high resolution HLA and SNP haplotype map for disease association studies in the extended human MHC. Nature Genetics doi:10.1038/ng1885

A complete list of the study's authors and their affiliations:

Paul I.W. de Bakker(1,2,16), Gil McVean(3,16), Pardis C. Sabeti(1,16), Marcos M. Miretti(4,16), Todd Green(1), Jonathan Marchini(3), Xiayi Ke(5), Alienke J. Monsuur(6), Pamela Whittaker(4), Marcos Delgado(4), Jonathan Morrison(4), Angela Richardson(1), Emily C. Walsh(1), Xiaojiang Gao(7), Luana Galver(8), John Hart(9), David A. Hafler(10), Margaret Pericak-Vance(9), John A. Todd(11), Mark J. Daly(1,2), John Trowsdale(12), Cisca Wijmenga(6), Tim J. Vyse(13), Stephan Beck(4), Sarah Shaw Murray(8), Mary Carrington(7), Simon Gregory(9), Panos Deloukas(4), John D. Rioux(1,14,15)

Program in Medical and Population Genetics, Broad Institute of Harvard and MIT, Cambridge, Massachusetts, USA

Center for Human Genetic Research, Massachusetts General Hospital, Boston, Massachusetts, USA

Department of Statistics, University of Oxford, Oxford, United Kingdom

Wellcome Trust Sanger Institute, Hinxton, United Kingdom

Wellcome Trust Centre for Human Genetics, University of Oxford, United Kingdom

Complex Genetics Section, Department of Medical Genetics, University Medical Center Utrecht, The Netherlands

Laboratory of Genomic Diversity, SAIC-Frederick, Inc., NCI-Frederick, Frederick, Maryland, USA

Illumina, Inc., San Diego, California, USA

Center for Human Genetics, Duke University Medical Center, Durham, North Carolina, USA

Brigham and Women's Hospital, Department of Neurology, Boston, Massachusetts, USA

Juvenile Diabetes Research Foundation/Wellcome Trust Diabetes and Inflammation Laboratory, Cambridge Institute for Medical Research, University of Cambridge

Cambridge Institute for Medical Research, Addensbrookes Hospital, Hills Road, Cambridge, UK

Imperial College of London, London, United Kingdom

Université de Montréal, Department of Medicine, Montréal, Québec, Canada

Montreal Heart Institute, Montréal, Québec, Canada

About the Montreal Heart Institute
Founded in 1954, the Montreal Heart Institute constantly aims for the highest standards of excellence in the cardiovascular field through its leadership in prevention, ultra-specialized care, training of professionals, clinical and fundamental research, and assessment of new technologies. It is affiliated with the Université de Montréal and its clinical outcomes are among the best in the world. The MHI Research Centre officially came into existence in 1976 and has made enormous strides since its creation. Today, there are approximately 450 employees, students and researchers at the MHI Research Center. The MHI's outstanding feature is the balance it achieves between basic research, clinical research and clinical care. Its prime focus areas of research are vascular diseases, myocardial function and electrophysiology. Genomics (including pharmacogenomics), biomarkers and preventive cardiology are other areas of focus.

About the Université de Montréal
Founded in 1878, the Université de Montréal today has 13 faculties and together with its two affiliated schools, HEC Montréal and École Polytechnique, constitutes the largest centre of higher education and research in Québec, the second largest in Canada, and one of the major centres in North America. It brings together 2,400 professors and researchers, accommodates nearly 55,000 students, offers some 650 programs at all academic levels, and awards about 3,000 masters and doctorate diplomas each year.

About the Broad Institute of MIT and Harvard
The Broad Institute of MIT and Harvard was founded in 2003 to bring the power of genomics to biomedicine. It pursues this mission by empowering creative scientists to construct new and robust tools for genomic medicine, to make them accessible to the global scientific community, and to apply them to the understanding and treatment of disease.

The Institute is a research collaboration that involves faculty, professional staff and students from throughout the MIT and Harvard academic and medical communities. It is jointly governed by the two universities.

Organised around Scientific Programs and Scientific Platforms, the unique structure of the Broad Institute enables scientists to collaborate on transformative projects across many scientific and medical disciplines.

Source: The University of Montreal
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Thoughts on gene research

Postby lyndacarol » Mon Sep 25, 2006 5:20 pm

I readily admit that I am "technologically impaired" and unscientific, but I have always wondered about the oft-mentioned genetic component to MS. Why can't a blood sample be drawn by the neuro at the time of diagnosis, analyzed for the gene-mapping (that was so touted in recent years), and simply be compared with thousands of others (There is already a database in Phoenix of several thousand MS patients.)? Couldn't an area in common on the genome be found more easily that way? After all, in this age of computers wouldn't that be quite possible?

Just the ruminations of an idle mind!
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Postby scoobyjude » Mon Sep 25, 2006 7:22 pm

Sounds like a completely logical question to me. Even though they don't know what causes MS you would think they'd at least be able to definitely diagnose it and then study our differences.
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