New York Times
SCIENCE
| August 20, 2010
Reanimated 'Junk' DNA Is Found to Cause Disease
By GINA KOLATA
For the first time, geneticists report, they have seen a dead gene come
back to life and cause a disease, a common form of muscular dystrophy.
|
An international
collaboration identifies a region of DNA necessary for FSHD and focuses
attention on DUX4 as the cause of muscle deterioration by Dr. Stephen Tapscott
An
international research collaboration that includes research groups funded by
the Friends of FSH Research has made a critical advance in determining the
cause of facioscapulohumeral dystrophy (FSHD).
The mutation that causes the majority of FSHD cases was identified
almost two decades ago but, in contrast to most genetic diseases, knowledge of
the genetic mutation did not explain the cause of the disease. Although many different models and hypotheses
were proposed for how the FSHD mutation might cause the disease, none had
sufficient experimental support to attain legitimacy, which resulted in
controversy and slow progress in FSHD research. The recent publication in
Science magazine focuses research on a single and testable hypothesis. Their
work identified a DNA variation (polymorphism) necessary for FSHD that occurs
outside the mutation region and is necessary for FSHD. This DNA sequence in individuals susceptible
to FSHD acts to stabilize the product of the DUX4 gene, whereas individuals not
susceptible to FSHD have a different DNA sequence that does not stabilize
DUX4. This finding provides a new and
unifying model for FSHD because it focuses studies on determining whether the
DUX4 protein causes FSHD, as indicated by this group's genetic analysis.
This study,
published in Science magazine, was led by Dr. Silvere van der Maarel at the
Leiden University Medical Center, together with Dr. Rabi Tawil at the
University of Rochester, Dr. Stephen Tapscott at the Fred Hutchinson Cancer
Research Center in Seattle, and Dr. Dan Miller at the University of Washington
in Seattle. Rapid progress was made possible by an unusual degree of
collaboration and data-sharing among the individual groups at yearly workshops
sponsored by the Friends of FSH research.
The Friends of FSH Research, as well as the Shaw Family Foundation,
sponsored yearly workshops that brought these collaborators together to share
their research and also funded research in the laboratories of two of the
groups (Dr. Stephen Tapscott at the Fred Hutchinson Research Center and Dr.
Daniel Miller at the University of Washington). The initial progress supported
by the Friends of FSH Research resulted in successful grant applications to the
National Institutes of Health to continue their FSHD research studies. |