Most chromosomes have been around for millions of years. However, researchers from the Stowers Institute for Medical Research have revealed the dynamics of a new, very young chromosome in fruit flies that is similar to chromosomes that arise in humans and is associated with treatment-resistant cancer and infertility. The researchers say the findings may lead to developing more targeted therapies for treating these conditions.
A new study published in Current Biology reveals how this small chromosome that arose less than 20 years ago has persisted in a single, lab-reared strain of the fruit fly, Drosophila melanogaster, and is correlated with supernumerary (extra) chromosomes in humans.
“I feel kind of like an astronomer who’s watching the birth of a star,” said Stowers’ investigator Scott Hawley.
“We are getting to watch the birth of a chromosome and are starting to understand both its capabilities and limitations.”
Previous research from the Hawley Lab had first identified these small, extra chromosomes, but little was known about their form, function, or dynamics during cell division. Former Hawley Lab postdoctoral researcher Stacey Hanlon realized that this discovery could be an ideal system to investigate how new chromosomes arise, which may lead to methods to overcome infertility and more effective cancer treatments.
Supernumerary chromosomes in humans are found in cancer cells and frequently interfere with drugs designed to target tumors, making these types of cancers, like osteosarcoma, difficult to treat. In addition, the presence of supernumerary chromosomes in men can disrupt normal chromosome segregation during sperm production, which can cause infertility.
“Being able to understand how supernumerary chromosomes arise and what their structures are, can potentially illuminate their vulnerabilities,” Hawley said.
“This may enable the development of potential therapeutic targets.”
Called B chromosomes, – as opposed to the standard “A” set of essential chromosomes – these genetic elements naturally appeared in a single laboratory stock of fruit flies in Hawley’s lab. Now, the researchers are witnessing chromosome birth and evolution in less than two decades.
“I like to call these B chromosomes genetic renegades,” said Hanlon.
“They do not follow the rules.”
Hanlon discovered that the fruit fly B chromosomes are maintained by a mechanism called “meiotic drive” that enables them to rebel against the usual rules of inheritance. The B chromosomes drive their way into the next generation during the formation of the egg to ensure their own persistence in more than half of the next generation.
“Their genetic background – meaning the unique features in the B chromosome flies’ genetic make-up – supports their preferential transmission to the next generation,” said Hanlon.
“That buys these guys evolutionary time to become a new chromosome, whether that’s picking up an essential gene or acquiring something that enables them to better cheat.”
Importantly, meiotic drive is a powerful force that can shape how genomes evolve. These findings originating in the Hawley Lab and actively investigated by Hanlon, now in her own lab at the University of Connecticut, can be used to understand the mechanisms behind what keeps meiosis fair, and ensures that cheaters like the B chromosomes, do not gain an advantage.
Additionally, Hanlon is examining how specific mutations can lead to chromosome breakage and new chromosome formation, revealing the mechanism of how supernumeraries arise and become requisite components of a genome.
“We’re always looking for Achilles heels to get rid of these kinds of things,” said Hawley of problematic supernumeraries in humans.
“If we can identify what encouraged their formation, we may be able to identify individuals more likely to form them and take better measures to look for and deal with them.”
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