MSU lands NIH grant to study connection between fish genes and human medicine
- Mar 23, 2017
- Faculty & Staff, Research, Integrative Biology
Ingo Braasch (center) and postdocs Solomon David (left) and Andrew Thompson are using the spotted gar to open pathways to advancments in human biomedical research.
Michigan State University has landed a $727,000 grant from the National Institutes of Health to improve the use of fish as disease models for human medicine.
Ingo Braasch, MSU integrative biologist in the College of Natural Science who’s leading the MSU efforts of this collaborative grant that also includes the University of Oregon and Nicholls State University (Louisiana), will focus on the spotted gar, which has a similar genome to humans and zebrafish, a popular biomedical fish model. The ancient, slowly evolving spotted gar can serve as a "bridge species" between human and zebrafish, thereby opening pathways to important advancements in human biomedical research.
“There are potentially thousands of connections that can be made from human to zebrafish and back through gar as a steppingstone that could not be done by comparing human and zebrafish directly,” Braasch said. “This points to a better way to perform biomedical research for studying human disease in zebrafish. With higher precision, researchers will be able to find the right region in the genome of zebrafish to design experiments and mutation models.”
Genome-wide association studies, or GWAS, have detected thousands of genetic variations near hundreds of genes associated with numerous human diseases. The problem is that scientists don’t know which gene near a GWAS region in the human genome may cause the disease. Comparative medicine, using rearranged genomes of fish models to test hypotheses, can help locate those troublesome intersections and lead to personalized approaches to investigate and potentially treat those diseases.
Zebrafish are often used as model fish in biomedical research, but due to their genetic divergence from humans it can be difficult to make direct biological comparisons.
Braasch believes the spotted gar can help biomedical researchers make the jump. He hopes to develop additional resources to help identify disease-associated genetic region in humans. In turn, researchers can then locate the corresponding region in spotted gar and then investigate the appropriate location in the genomes of zebrafish or other fish models.
Gar embryos (pictured above) are being studied by researchers to improve the use of fish as disease models for human medicine.
Yes, but what makes gar so special?
First, ever since the fish and human lineages split about 450 million years ago, the gar genome has not changed as much as that of more modern fish like zebrafish. Second, gars also offer a window into the evolution of vertebrate anatomy because their body plan has not changed as much as those of modern fish. Gar helps to understand how fins evolved into limbs that allowed fish to walk on land and how enamel on our teeth evolved from ancient types of fish scales, which are still found in gar.
“We are using gar to further improve comparisons of humans to zebrafish to make zebrafish an even better model system for disease research,” Braasch said. “And by studying gar, zebrafish and other fishes side-by-side, we also hope to answer many more evolutionary questions about the origin of vertebrate genomes and their biology.”