The gene appears to be essential for proper development of part of the nervous system, they report in the
January, 1998, issue of Nature Genetics. The scientists expect to find that the equivalent human gene, when
mutated, also causes Hirschsprung disease in people, as has been the case with the four previously discovered
mouse Hirschsprung genes.
Hirschsprung disease is a highly variable inborn disorder whose chief feature is impaired intestinal function in
which part of the colon lacks nerve cells and so is unable to relax. The result is chronic constipation and distention
of the abdomen. The disorder, which affects about one in 5,000 US newborns, is usually diagnosed in infancy.
Treatment involves surgical removal of the affected portion of the colon.
The scientists believe the product of the newly identified gene, which they call SOX10, is one of many
transcription factors proteins that control which genes are expressed at any given time in any given tissue. The
SOX10 protein appears in the very early embryo in the cells that will eventually become the peripheral nervous
system (the nerves that conduct impulses to and from the spinal cord).
"By studying this gene and what genes it regulates we will really have an insight into the early development of the
peripheral nervous system. So, in addition to its relevance for Hirschsprung's disease, this finding will provide a
powerful tool to be used for future studies," said corresponding author William J. Pavan.
Dr. Pavan heads the mouse embryo section of NHGRI's Laboratory of Genetic Disease Research, where the study was done.
NHGRI oversees the NIH's role in the Human Genome Project, an international research effort to develop tools
for gene discovery.
For more information or to arrange an interview with Dr. Paven, contact Jeff Witherly at (301) 402-8564 or
Galen Perry at (301) 402-3035.
The NHGRI website contains this and many other genetic story ideas and press releases at www.nhgri.nih.gov.