Long stretches of DNA once considered inert dark matter
appear to be uniquely active in a part of the brain known to control
the body’s 24-hour cycle, according to researchers at the National
Institutes of Health.
Working with material from rat brains, the researchers found some
expanses of DNA contained the information that generate biologically
active molecules. The levels of these molecules rose and fell, in
synchrony with 24-hour cycles of light and darkness. Activity of some
of the molecules peaked at night and diminished during the day, while
the remainder peaked during the day and diminished during the night.
The material came from the brain structure known as the pineal gland.
Located in the center of the human brain, the pineal gland helps
regulate the body’s responses to day and night cycles, the researchers
explained. In the evenings and at night, the pineal gland increases
production of melatonin, a hormone that synchronizes the body’s rhythms
with the cycle of light and dark. In many species, the pineal gland
also plays a role in seasonally associated behaviors, such as
hibernation and mating, as well as in sexual maturation.
The biologically active material arising from the pineal gland DNA is
called long noncoding RNA (lncRNA). The lncRNA is distinct from the
better-known messenger RNA (mRNA), which serves as a kind of template to
translate the information contained in DNA for the manufacturing of
proteins. The lncRNAs appear instead to be involved in activating,
blocking or altering the activity of genes or influencing the function
of the proteins, or acting as scaffolds for the organization of
complexes of proteins. The researchers’ use of next-generation
sequencing methods detected the lncRNA activity in addition to the mRNA
they originally targeted, which helped them in making their discovery.
"These lncRNAs come from areas of the genome that we thought were
quiet," said senior author David Klein, Ph.D., head of the Section on
Neuroendocrinology at the NIH's Eunice Kennedy Shriver National
Institute of Child Health and Human Development (NICHD), in much of the
research was conducted. "But current research in the field makes it
unequivocally clear that the information-carrying capacity of the
genome is a lot greater than we realized previously."
The
study was a collaboration between Dr. Klein and NIH colleagues at
the NICHD; the National Human Genome Research Institute (NHGRI); the NIH
Intramural Sequencing Center, administered by NHGRI and the Center for
Information Technology.
In addition, researchers from King’s College London; the University of
Copenhagen, in Denmark; the Genomatix Software company, in Munich
contributed to the study.
Their findings appear online in the Proceedings of the National Academy of Sciences.
To conduct their analysis, the researchers examined RNA from the
pineal glands of rats exposed to cycles of 14 hours of light and 10
hours of darkness. The researchers identified 112 lncRNAs with 24 hour
cycles. For nearly 60 percent of these lncRNAs, the rats' DNA produced
twice as many lncRNA molecules at night as during the day. In addition,
nearly 90 percent of the lncRNAs were produced in significantly greater
quantities in the pineal gland than in other tissues of the body, most
of which did not have detectable levels of these lncRNAs.
The researchers also disrupted the rats' regular day–night light
cycle by turning on a light during a typical dark period. Within 30
minutes of the light going on, most of the lncRNAs decreased by half.
The
role of the pineal gland lncRNAs is unclear; however, they have
circadian patterns of activity. Dr. Klein previously documented hundreds
of genes in the pineal gland with consistent day–night cycles of
activity.
"The lncRNAs show such strong activity, they obviously have something
to tell us about the biology of daily body rhythms," Dr. Klein said.
"We are only beginning to understand how the pineal gland helps maintain
the body's 24 hour rhythms."
No comments:
Post a Comment