Harvard: Life itself arose among the oscillations of the waves and the
oscillations between darkness and light. The oscillations are carried in
our heartbeats and in our circadian sleep patterns. A new study in Cell shows how these oscillations reach all the way down into our cells and help mastermind the timing of protein production. It’s a whole new layer of biology that could shed light on our
understanding of conditions such as cancer, autism and metabolic
disorders, which may involve disrupted protein production. And it grew out of research on tuberous sclerosis complex (TSC), a rare genetic disorder that often causes autism.
Altered sleep, altered proteins?
Jonathan Lipton,
HMS instructor of neurology and a sleep specialist at Boston Children’s
Hospital, was intrigued that children with TSC and other
neurodevelopmental disorders—including 50 to 90 percent of children with
autism—have significant sleep disturbances.
“These kids are waking up in the middle of the night for hours at a
time,” said Lipton. “This completely disrupts families’ lives and has
motivated my work in the lab. Why is sleep disruption such a major part
of these disorders?”
Lipton and Mustafa Sahin,
HMS associate professor of neurology who does research on TSC at Boston
Children’s FM Kirby Neurobiology Center, speculated that something is
wrong with these children’s circadian rhythms. TSC’s underlying biology
is fairly well understood, providing an opportunity to delve into this
question.
Lipton and Sahin began by looking at the mTOR pathway, a fundamental
cellular growth pathway that is overactivated in TSC. It regulates gene
transcription, the first step in making proteins. Sahin has shown that
in TSC, overactivation of mTOR causes neurons to develop abnormally and
form improper connections.
But is mTOR connected to circadian rhythms? In looking for a
connection, Lipton and Sahin found that mTOR—through another protein
called S6K1—regulates a protein called BMAL1 that is crucial for the
expression of circadian rhythms.
“It’s been known for about 15 years that without BMAL1, you can’t have circadian rhythms,” said Lipton.
Like two gears in a clock, the mTOR pathway cyclically activates
BMAL1, which then helps activate the cellular protein-making machinery
in the ribosomes, the researchers found. As a result, they observed
peaks and troughs of when proteins are made during a 24-hour day.
Delegating control
They further showed through their experiments that protein synthesis is turned on even when genes aren’t being transcribed.
“A whole part of circadian oscillation is at the level of the protein
synthesis machinery, and occurs independently of DNA transcription,”
said Sahin. “It’s another leg of the stool.”
Why is this important? Protein synthesis is fundamental to pretty
much everything our cells do hour to hour. The circadian system helps
make sure the right proteins are made at the right time—for example,
anticipating the liver enzymes you will need in the morning to digest
your breakfast.
“The single most important thing to test is how this will play out in
disease,” said Lipton, “particularly in disease in which protein
synthesis is implicated.”
If the timing of protein synthesis is thrown off, it could lead to
shortages of certain enzymes when they’re most needed, or cause
accumulations of proteins that aren’t needed.
Here are some disease scenarios Lipton is speculating about:
Neurodevelopmental disorders: Proteins are critical
in signaling at synapses, the junctions between neurons. Too much or too
little of a protein at a given time could disrupt brain function and
contribute to conditions like autism. (Since sleep disruption is common
in these disorders, a big question in the field is whether sleep
disruption is a byproduct or a cause, said Lipton.)
Metabolic disease: The making of enzymes at specific
times is key to our ability to break down food and other compounds.
“Problems with protein oscillations may disrupt cells’ ability to
dispose of metabolic byproducts,” said Lipton. “It can affect their
ability to handle physiological toxicity—like missing a trash pickup.”
Neurodegenerative diseases: The researchers
speculate that disorders such as Parkinson’s could result from a
mismatch between the timing of protein synthesis and synthesis of
enzymes to break the proteins down.
Cancer: Cancer cells are already known to have
dysregulated protein synthesis. Perhaps altered circadian regulation
adds to a cancer’s virulence by removing an important brake in the
system.
Additionally, knowing when certain enzymes are made could inform the
timing of drug therapy. Chronotherapeutics, a concept that began in the
cancer world as an attempt to reduce the side effects of chemotherapy,
takes advantage of these natural oscillations. Boston Children’s is
starting to incorporate it into epilepsy treatment.
Circadian rhythms are coming to be seen as a fundamental part of our
biology, and circadian or sleep disturbances have been linked to
obesity, diabetes, cardiovascular disease and even inflammation. Knowing
how the circadian clock interacts with protein synthesis could provide a
whole new angle on medicine.