A Genomic-Systems Biology Map for Cardiovascular Function

Author:

Stoll Monika1,Cowley Allen W.1,Tonellato Peter J.12,Greene Andrew S.1,Kaldunski Mary L.1,Roman Richard J.1,Dumas Pierre13,Schork Nicholas J.456,Wang Zhitao12,Jacob Howard J.13

Affiliation:

1. Department of Physiology,

2. Bioinformatics Research Center, and

3. Human and Molecular Genetics Center, Medical College of Wisconsin, 8701 Watertown Plank Road, Milwaukee, WI 53226–0509, USA.

4. Case Western Reserve University, Cleveland, OH 44106, USA.

5. The Jackson Laboratory, Bar Harbor, ME 04609, USA.

6. Harvard School of Public Health, Boston, MA 02115, USA.

Abstract

With the draft sequence of the human genome available, there is a need to better define gene function in the context of systems biology. We studied 239 cardiovascular and renal phenotypes in 113 male rats derived from an F 2 intercross and mapped 81 of these traits onto the genome. Aggregates of traits were identified on chromosomes 1, 2, 7, and 18. Systems biology was assessed by examining patterns of correlations (“physiological profiles”) that can be used for gene hunting, mechanism-based physiological studies, and, with comparative genomics, translating these data to the human genome.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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