Researchers in search of loci in the human genome that are
likely to contribute to the constellation of factors leading to hypertension have compared candidate loci in humans and rats IStoll, M., et al. (2000). New Target Regions for Human Hypertension via Comparative Genomics. Genome Res. $10: 473-482$ ]. Through this research, they identified 26 chromosomal regions that they consider likely to contain hypertension genes. How can comparative genomics aid in the identification of genes responsible for such a complex human disease? The researchers state that comparisons of rat and human candidate loci to those in the mouse may help validate their studies. Why might this be so?