Gene editing gone wrong: Scientists accidentally create angry hamsters
- Of all rodents, hamsters have a social organization and stress response that is most human-like.
- To study aggression in hamsters, a team of scientists used gene editing to create what they thought would be a calmer rodent. Instead, the gene-edited rodents were angrier — chasing, biting, and pinning down other same-sex hamsters.
- The research underscores that the field of behavioral genetics has a long way to go.
Hamsters have a social organization and stress response that is more human-like than any other rodent. Thus, behavioral scientists have relied on hamsters to understand the forces that govern behavior. According to a recent study, however, these forces are less well-understood than previously thought. The researchers used gene-editing technology to delete a receptor thought to cause aggression in hamsters. Instead of becoming more cuddly, however, the hamsters got mean.
A gene that regulates aggression
In 1984, a group of researchers set out to study the circadian rhythm by injecting small amounts of hormones into the brains of hamsters. One of the hormones, arginine vasopressin (AVP), had an immediate and surprising effect. It didn’t alter the hamsters’ sleep cycle, but it did induce a dramatic behavioral change. The hamsters began soaking their hips (where the scent glands are located) with saliva and rubbing themselves vigorously against the wall of the cage, a behavior indicative of aggressively claiming their territory.
Subsequent pharmacological studies thoroughly examined the function of AVP’s receptor, called Avpr1a. According to the studies, Avpr1a seemed to have sex-dependent effects. When male hamsters received injections of Avpr1a activators (such as AVP), they became more aggressive, whereas the female hamsters became less aggressive. Alternatively, when hamsters received injections of Avpr1a inhibitors, males became less aggressive, and females becomes more aggressive. Almost four decades of studies overwhelmingly showed that Avpr1a directly regulated aggression and anxiety-like behavior.
One study, however, created an air of mystery around Avpr1a. In 2007, a team of researchers at the University of Buffalo knocked out the Avpr1a gene in male mice, expecting the mice to show reduced aggression due to a lack of AVP signaling. However, the Avpr1a-lacking mice were no more or less aggressive than normal mice. For over a decade, this discrepancy was explained as being due to developmental compensation — that is, the embryo compensated for the lack of Avpr1a by modulating other behavioral pathways.
A team of researchers at Georgia State University led by Elliott Albers and Kim Huhman, however, disagreed. The major gripe that they had with the 2007 study was that Avpr1a was knocked out in mice, rather than hamsters. Such differences matter. So, the researchers used CRISPR-Cas9 gene-editing technology to mutate the Avpr1a receptor gene (so that it was no longer functional) in male and female hamsters.
The researchers believed that, by removing the hamster’s ability to make Avpr1a, the hamsters would become less aggressive. Their hypothesis was incorrect. To the contrary, all Avpr1a-lacking hamsters, regardless of sex, exhibited far more aggressive behavior, doing twice as much flank marking as well as chasing, biting, and pinning down other same-sex hamsters.
The authors did not expect angry hamsters. “This suggests a startling conclusion,” Albers said. “Even though we know that [AVP] increases social behaviors by acting within a number of brain regions, it is possible that the more global effects of the Avpr1a receptor are inhibitory. We don’t understand this system as well as we thought we did. The counterintuitive findings tell us we need to start thinking about the actions of these receptors across entire circuits of the brain and not just in specific brain regions.”