Visualization
of the genome (green) and a single gene (magenta) in a human cell nucleus, with
genomic motions mapped by arrows and an example of a gene trajectory
highlighted as a colored curve. Credit: Alexandra Zidovska, Department of
Physics, NYU.
A
team of scientists has discovered surprising connections among gene activity,
genome packing, and genome-wide motions, revealing aspects of the genome's
organization that directly affect gene regulation and expression.
The findings, reported in the journal Nature Communications, bolster the
understanding of the mechanics behind transcription-dependent motions of single
genes—the dysfunction of which may lead to neurological and cardiovascular
disorders as well as to cancer.
"The genome is 'stirred' by
transcription-driven motions of single genes," explains Alexandra
Zidovska, a professor of physics at New York University and the senior author
of the study.
"Genes move differently, depending on whether they are being read or not, leading to complex, turbulent-like motions of the human genome. Understanding the mechanics behind transcription-dependent motions of single genes in the nucleus might be critical for understanding the human genome in health and disease."
Motion
of a single gene (white dot) is marked by its trajectory (colored curve) within
the flows of the surrounding genome (arrows). Credit: Alexandra Zidovska,
Department of Physics, NYU.
The
human genome consists of two meters (six and a half feet) of DNA, which is
packed inside the cell in a nucleus barely 10 micrometers in diameter—or
100,000 times smaller than the length of the genome's DNA. The DNA molecule
encodes information for all cellular processes and functions, with genes serving as units of
information.
Different genes are read, and their
information is processed at different times. When a gene is being read, there
is molecular machinery that accesses it and transcribes its information into an
mRNA molecule, a process known as transcription.
It had previously been discovered, by Zidovska and her colleagues, that the genome
undergoes a lot of "stirring," or movement, leading to its
reorganization and repositioning in the nucleus.
Motions (arrows) of the human genome across an
entire cell nucleus. Credit: Alexandra Zidovska,
Department of Physics, NYU.
However, the
origin of these motions is little understood. Scientists have hypothesized that
molecular motors fueled by adenosine
triphosphate (ATP) molecules, which provide energy for many
biological processes, are the drivers.
These active
motors are thought to apply forces on DNA, which can lead to a motion of DNA
and the nucleoplasm—its surrounding fluid. But the larger physical machinations
behind it remain elusive.
With this in
mind, Zidovska and her colleagues focused on RNA polymerase II—responsible for
the transcription and one of the most abundant molecular motors in the cell
nucleus. When a gene is active, i.e. actively transcribed, the
responsible molecular machinery applies forces on DNA
during its processing.
The Nature
Communications study investigated how a motion of a single actively
transcribed gene affects the motions of the genome around it in live human
cells.
To do so, the
authors employed CRISPR technology to fluorescently label single genes,
two-color high-resolution live cell microscopy to visualize the motion of these
labeled genes, and displacement correlation spectroscopy (DCS) to
simultaneously map flows of the genome across the nucleus.
The
high-resolution imaging data were then processed through a physical and mathematical
analysis, uncovering a never-before-seen physical picture of how
genes move inside the cell.
In their
study, the researchers initially examined the motions of the genes—when they
are inactive—then "switched" these genes on and observed how their
motion changes once "active." At the same time, the authors used DCS
to map flows of the surrounding genome, monitoring how the genome flows across
the nucleus before and after gene activation.
Overall, the
authors found that active genes contribute to the stirring motion of the
genome. Through simultaneous mapping of single-gene and genome-wide motions,
they reveal that the compaction of the genome affects how the gene is
contributing.
Specifically,
a motion-correlation analysis indicated that a single active gene drives the
genome's motion in low-compaction regions, but a high-compaction genome drives
gene motion regardless
of its activity state.
"By
revealing these unexpected connections among gene
activity, genome compaction, and genome-wide motions, these findings
uncover aspects of the genome's spatiotemporal organization that directly
impact gene regulation and expression," says
Zidovska.
The work also
adds to our understanding of physics.
"This
research provides new insights into the physics of active and living
systems," she observes. "By revealing an emergent behavior of active
living systems, such as the human genome, it teaches us new physics."
The paper's other authors were Fang-Yi Chu and Alexis S. Clavijo, NYU doctoral students, and Suho Lee, an NYU postdoctoral researcher.
Source: Scientists uncover how transcription drives motion within the genome
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