Learning the alphabet of gene control
Karolinska Institutet |
Scientists at Karolinska Institutet in Sweden have made a large
step towards the understanding of how human genes are regulated. In a new
study, published in the journal Cell, they identified the DNA
sequences that bind to over four hundred proteins that control expression of
genes. This knowledge is required for understanding of how differences in
genomes of individuals affect their risk to develop disease. After the human
genome was sequenced in 2000, it was hoped that the knowledge of the entire
sequence of human DNA could rapidly be translated to medical benefits such as
novel drugs, and predictive tools that would identify individuals at risk of
disease. This however turned out to be harder than anticipated, one of the
reasons being that only 1 percent of the genome that code for proteins was in
fact possible to read. The remaining part, much of which describes how these
proteins should be expressed in different cells and tissues, could not be
understood. This, in turn, because the scientists did not know which DNA
sequences are functional, and bind to the specific proteins called
transcription factors that regulate gene expression.
"The
genome is like a book written in a foreign language, we know the letters but
cannot understand why a human genome makes a human or the mouse genome a
mouse," says Professor Jussi Taipale, who led the study at the Department
of Biosciences and Nutrition. "Why some individuals have higher risk to
develop common diseases such as heart disease or cancer has been even less
understood."
The human genome encodes approximately 1000 transcription
factors, and they bind specifically to short sequences of DNA, and control the
production of other proteins. In the work published in Cell, the scientists at Karolinska Institutet
describe DNA sequences that bind to over 400 such proteins, representing
approximately half of all human transcription factors. Data was generated with
a new method that uses a modern DNA sequencer that produces hundreds of millions
of sequences, giving the results unprecedented accuracy and reliability.
In
addition, binding specificities of human transcription factors were compared to
those of the mouse. Surprisingly, no differences were found. According to the
scientists, these results suggest that the basic machinery of gene expression
is similar in humans and mice, and that the differences in size and shape are
caused not by differences in transcription factor proteins, but by presence or
absence of the specific sequences that bind to them.
"Taken
together, the work represents a large step towards deciphering the code that
controls gene expression, and provides an invaluable resource to scientists all
over the world to further understand the function of the whole human
genome," says Professor Taipale. "The resulting increase in our
ability to read the genome will also improve our ability to translate the
rapidly accumulating genomic information to medical benefits.
Source: Karolinska
Institutet
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