Why is model organism research important?


Begun in 1990, the U.S. Human Genome Project is a 15-year effort coordinated by the U.S. Department of Energy and the National Institutes of Health to Identify all the estimated 80,000 genes in human DNA, Determine the sequences of the 3 billion chemical bases that make up human DNA, store this information in databases, and develop tools for data analysis. To help achieve these goals, researchers also are studying the genetic makeup of several nonhuman organisms. These include those species:

  • Human 3000 million bases (60,000 to 80,000 genes)
  • Mouse 3000 million bases (50,000 to 100,000 genes)
  • Drosophila (fruit fly) 165 million bases (15,000 to 25,000 genes)
  • Nematode (roundworm) 100 million bases (11,800 to 13,800 genes)
  • Yeast (fungus) 14 million bases (8355 to 8947 genes)
  • E. coli (bacteria) 4.67 million bases (3237 genes)
  • H. influenzae (bacteria) 1.8 million bases
  • M. genitalium (bacteria) 0.58 million bases

Model organisms offer a cost-effective way to follow the inheritance of genes (that are very similar to human genes) through many generations in a relatively short time. Some model organisms being studied in HGP are the bacterium Escherichia coli, yeast Saccharomyces cerevisae, roundworm Caenorhabditis elegans, fruit fly Drosophila melanogaster, and laboratory mouse. Additionally, HGP spinoffs have led to genetic analysis of other environmentally and industrially important organisms in the United States and abroad.

Example:

Of Mice and Humans:

The Value of Comparative Analyses A remaining challenge is to recognize and discriminate all the functional constituents of a gene, particularly regulatory components not represented within cDNAs, and to predict what each gene may actually do in human biology. Comparing human and mouse sequences is an exceptionally powerful way to identify homologous genes and regulatory elements that have been substantially conserved during evolution. Researchers led by Leroy Hood (University of Washington, Seattle) have analyzed more than one million bases of sequence from T-cell receptor (TCR) chromosome regions of both human and mouse genomes. Many subtle functional elements can be recognized only by comparing human and mouse sequences. TCRs play a major role in immunity and autoimmune disease, and insights into their mechanisms may one day help treat or even prevent such diseases as arthritis, diabetes, and multiple sclerosis (possibly even AIDS).