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January/February 2018^ DISCOVER^33

CLOCKWISE FROM TOP: CLAUS LUNAU/SCIENCE SOURCE; EADWEARD MUYBRIDGE/LIBRARY OF CONGRESS; SETH SHIPMAN


CRISPR Goes to the Movies



EADWEARD MUYBRIDGE’S
“The Horse in Motion” was
an early demonstration
of stop-motion illustration. In
keeping with his pioneering spirit,
Harvard University researchers have
re-created the images by storing
data in living bacteria. The results
were published in Nature in July.
Geneticist Seth Shipman and
his team translated the pixels of
Muybridge’s moving picture into
a code made from the As, Ts, Gs,

and Cs of DNA. Then, using the
CRISPR-Cas gene-editing tool, they
spliced sequences corresponding
to individual video pixels into the
genome. The bacteria strung these
snippets together in order and
stored them in its DNA, letting
scientists replay the video.
Now that they’ve shown
it’s possible to encode
and retrieve information
sequentially in bacteria,
Shipman hopes to create

“molecular recorders” — genetically
engineered cells with a time log of
their activities. These recorders could
someday monitor cellular activities
in our bodies — like an airplane’s
black box — giving scientists insights
into what cells are doing and when.
— CARL ENGELKING

Age Is Just a Number


(of Neural Stem Cells)



SCIENTISTS MAY HAVE IDENTIFIED how to
slow or even reverse our biological clock. Adult
neural stem cells in the hypothalamus — a brain
region that regulates hunger, sleep, body temperature
and other activities — appear to orchestrate
the body’s aging process, they found.
Research on lab animals has shown
that the number of hypothalamus
stem cells diminishes with age. To
determine if this cell loss was
related to aging, scientists killed
off hypothalamic stem cells in
middle-aged mice, according to a
study that appeared in July in Nature.
The mice showed clear signs of aging,
such as loss of memory, endurance
and coordination.

The scientists also discovered that the stem cells
released tiny packets of microRNA, bits of genetic
material that control how genes function. They injected
the mRNA into the middle-aged mice that were missing
hypothalamic stem cells and into healthy
mice of similar age. In both groups,
the treatment slowed aging.
The findings could lead
to better methods of
treating age-related maladies
and prolonging life, says lead
author Dongsheng Cai of
the Albert Einstein College
of Medicine. “But it will take
some time to translate this
into humans,” he says.
— LINDA MARSA

Researchers
encoded the
series “The Horse
in Motion” (right)
and stored the
data in a bacterial
genome for later
replay (left).

Hypothalamus
Free download pdf