Two studies refute an enzyme’s essential role in remembering and forgetting
January 3, 2013 |
The excitement around the enzyme, called protein kinase M-ζ (PKM-ζ), started building in 2007, when Todd Sacktor at the SUNY Downstate Medical Center in New York City wiped out month-old memories
of unpleasant smells in rats. He did so by injecting their hippocampus — a region of the brain crucial in memory formation — with ZIP, a small peptide that is meant to block
Other teams obtained similar results, erasing different types of memory by injecting ZIP into various brain regions in rodents, flies and sea slugs. And in 2011, Sacktor did the opposite: he
strengthened rats' memory of unpleasant tastes by injecting their brains with viruses carrying extra
copies of PKM-ζ.
These fascinating studies suggested that long-term memory, rather than being static and stable, is surprisingly fragile, and depends on the continuous activity of a single enzyme.
Richard Huganir of Johns Hopkins University in Baltimore, Maryland, was intrigued by these results, but was concerned that much of the data depended on the actions of ZIP. He and his
collaborators took a different route, by deleting two genes — one for PKM-ζ and one for a related protein called PKC-ζ — in embryonic mice. Working independently, Robert Messing and
colleagues at the University of California, San Francisco, created similar mice.
Neither group of mice showed any memory problems. Messing’s animals formed persistent memories for fears, objects, places and movements across a battery of behavioral tests. And Huganir’s mice
showed normal levels of long-term potentiation — the strengthening of synapses between two neurons that is thought to underlie learning and memory.
“Our study pretty conclusively says that PKM-ζ does not regulate memory,” says Huganir. “We were quite surprised.” Even more surprisingly, both teams found that ZIP could still disrupt
established memories in their mice, despite their lack of PKM-ζ.
“Our study doesn’t rule out the possibility that PKM-ζ may play a role in some forms of memory, but it is not the essential master regulator of memory that the current literature suggests it to
be,” says Lenora Volk, a member of Huganir’s team.
But Sacktor argues that the results are “not too surprising” because a different gene might have compensated for the loss, as routinely happens in mice that have had some genes deleted. He
suspects that related proteins like PKM-ι or PKM-λ may be involved. “I think the future will be to try to find the back-up mechanisms for memory.”
However, Huganir’s team also created mice whose PKM-ζ gene could be deleted at will by giving them a specific drug. This allowed the researchers to deplete the enzyme during adulthood, after mice
had grown up with normal levels. The animals still showed normal long-term potentiation.
“These results do not show that PKM-ζ is unimportant,” says Lynn Nadel, a cognitive scientist at the University of Arizona in Tucson. “But they show that the situation is
complicated—surprise!—and that there are multiple possible pathways involved.”
These other pathways are still a mystery. Without PKM-ζ, “there are not many compelling alternatives for how long-term memory is maintained,” says Huganir. His team is now trying to explore other
mechanisms by identifying ZIP’s true targets. “The mechanisms underlying the maintenance of long-term memory will be one of the more exciting areas of neuroscience research for many years to
come,” he says.
This article is reproduced with permission from the magazine Nature.