ÖŲæŚĪ¶SM

Cracking the code on human obesity: U of T researchers discover fruit flies may have the answer

Photo of Fruit Fly
University Professor Marla Sokolowski: ā€œThe fly has been an excellent model organism to understand mammalian behaviour and metabolism, and so this work can point to places to look further in humansā€ (photo by Martin Cooper via Flickr)

A ÖŲæŚĪ¶SM study on fruit flies has uncovered a gene that could play a key role in understanding obesity in humans.

The paper published online this month in Genetics examines a ā€œforaging geneā€ humans share in common with fruit flies. The gene plays multiple roles, and it is found in the same locations for both fruit flies and humans ā€“ the nervous system, muscle and fat.

ā€œWhat our study does is nails the gene for being very important for the traits of moving, feeding and fat storage,ā€ says Marla Sokolowski of the department of ecology & evolutionary biology at U of Tā€™s Faculty of Arts & Science.

In nature, fruit flies called rovers with high amounts of the gene tend to move a lot, eat very little and stay lean, while flies with low amounts of the gene called ā€œsittersā€ are the opposite. The ā€œforaging geneā€ encodes a cell signalling molecule called a cGMP dependent protein kinase. 

The same could apply to obesity in humans.

ā€œWhen we say the ā€˜foraging geneā€™ is the same, what weā€™re saying is that when you look at the DNA sequences of the human and the fly there is a lot of similarity, enough that you can see itā€™s the fly version of the gene that the human has,ā€ says Sokolowski, a .

ā€œSo you could imagine if you are a fly, preferences for sugar, the tendency to store a lot of fat and the tendency to move less could all be contributing to the likelihood of being more obese if you have low levels of this gene, or to be leaner if you have higher levels.ā€

Such similarities between species are known as orthologs, meaning they are genes that evolved from a common ancestor eons ago.

When scientists first started mapping human genomes and comparing them to other organisms, they were shocked to discover humans donā€™t have that many more genes than flies do.

Sokolowski says the research is another part of the puzzle, and the beginning of our understanding of how what was once considered ā€œjunk DNAā€ is actually very important for regulating key characteristics such as behaviour and metabolism.

ā€œNo one has analyzed it in the way we have in flies, but itā€™s a hint from the fly. The fly has been an excellent model organism to understand mammalian behaviour and metabolism, and so this work can point to places to look further in humans.ā€

The study involved a technique called recombineering to manipulate DNA at the molecular level, so as to remove and then reinsert the gene in various doses to see the effects on behaviour and metabolism.

Lead author Aaron Allen was a PhD student in cell & systems biology at U of T when the work was done, and he was assisted by Sokolowski, fellow U of T student Ina Anreiter, and Oxford University collaborator Megan Neville, who taught Allen the technique.

ā€œThis kind of work is actually so cutting-edge that it takes a really good student to learn how to do this and then bring the technique back to the lab,ā€ says Sokolowski.

ā€œTo be able to take a gene of this large size and complexity and put it back in the fly so that it works is almost at the edge of what is possible.ā€ 

Sokolowski says itā€™s particularly interesting that one gene should have multiple roles in feeding and obesity in the body, a characteristic known as pleiotropy.

The next question would be how exactly it plays multiple roles.

ā€œLots of genes have multiple roles, but the idea here is that this gene may be involved in the coordination of roles in traits important for feeding and obesity,ā€ she says.

ā€œWe donā€™t know much about pleiotropy, or how it happens, or how itā€™s regulated at the level of the molecules. So this sets the groundwork to be able to look at that in detail.ā€

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