TY - JOUR
T1 - BN phenome
T2 - Detailed characterization of the cardiovascular, renal, and pulmonary systems of the sequenced rat
AU - Kwitek, Anne E.
AU - Jacob, Howard J.
AU - Baker, John E.
AU - Dwinell, Melinda R.
AU - Forster, Hubert V.
AU - Greene, Andrew S.
AU - Kunert, Mary Pat
AU - Lombard, Julian H.
AU - Mattson, David L.
AU - Pritchard, Kirkwood A.
AU - Roman, Richard J.
AU - Tonellato, Peter J.
AU - Cowley, Allen W.
PY - 2006/4/13
Y1 - 2006/4/13
N2 - The postgenome era has provided resources to link disease phenotypes to the genomic sequence, i.e., creating a disease "phenome." Our detailed characterization of the sequenced BN rat strain (BN/NHsdMcwi) provides the first concerted effort in creating a direct link between a sequenced genome and its resulting biology. For the BN sequence to be of broad value to investigators, these measures need to be put into the context of the spectrum of the laboratory rats, so that their physiology can be benchmarked against the sequenced BN. As a major step in generating a comprehensive cardiovascular and pulmonary disease phenome, we measured 281 traits related to diseases of the heart, lung, and blood (http://pga.mcw.edu) in the sequenced BN. We compared these data with those of the same traits measured across multiple genetic backgrounds, both genders, and differing environments. We show that no single strain, inbred or outbred, can be considered a physiological control strain; what is normal depends on what trait is being measured and the strains' genome backgrounds. We find vast differences between the genders, also dependent on genome background. By combining the values across all strains studied, we generated a "population" mean and normal range of values for each of these traits, which are more genetically representative than the measured values in any single inbred or outbred strain. These data provide a baseline for physiological comparison of traits related to cardiovascular, lung, blood, and renal function in the sequenced BN rats relative to the major strains of rats studied in biomedical research.
AB - The postgenome era has provided resources to link disease phenotypes to the genomic sequence, i.e., creating a disease "phenome." Our detailed characterization of the sequenced BN rat strain (BN/NHsdMcwi) provides the first concerted effort in creating a direct link between a sequenced genome and its resulting biology. For the BN sequence to be of broad value to investigators, these measures need to be put into the context of the spectrum of the laboratory rats, so that their physiology can be benchmarked against the sequenced BN. As a major step in generating a comprehensive cardiovascular and pulmonary disease phenome, we measured 281 traits related to diseases of the heart, lung, and blood (http://pga.mcw.edu) in the sequenced BN. We compared these data with those of the same traits measured across multiple genetic backgrounds, both genders, and differing environments. We show that no single strain, inbred or outbred, can be considered a physiological control strain; what is normal depends on what trait is being measured and the strains' genome backgrounds. We find vast differences between the genders, also dependent on genome background. By combining the values across all strains studied, we generated a "population" mean and normal range of values for each of these traits, which are more genetically representative than the measured values in any single inbred or outbred strain. These data provide a baseline for physiological comparison of traits related to cardiovascular, lung, blood, and renal function in the sequenced BN rats relative to the major strains of rats studied in biomedical research.
KW - BN/NHsdMcwi rat strain
KW - Phenome
KW - Physiological genomics
UR - http://www.scopus.com/inward/record.url?scp=33645761913&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=33645761913&partnerID=8YFLogxK
U2 - 10.1152/physiolgenomics.00288.2005
DO - 10.1152/physiolgenomics.00288.2005
M3 - Article
C2 - 16478827
AN - SCOPUS:33645761913
SN - 1094-8341
VL - 25
SP - 303
EP - 313
JO - Physiological Genomics
JF - Physiological Genomics
IS - 2
ER -