New gene linked to congenital heart defects

December 17, 2009

( -- Researchers from the UC San Diego School of Medicine and colleagues have identified a new gene, ETS-1, that is linked to human congenital heart defects. The landmark study, recently published online in the journal of Human Molecular Genetics, provides important insights into some of the most prevalent forms of congenital heart defects in humans, including ventricular septal defects and potentially hypoplastic left heart syndrome, a uniformly fatal heart abnormality.

"Identification of this gene may have implications for prevention of some of these most common types of congenital ," said Dr. Paul Grossfeld, associate professor of pediatrics for the UC San Diego School of Medicine and pediatric cardiologist for Rady Children's Hospital-San Diego.

The researchers performed high-resolution chromosomal microarray mapping on human patients identified with the 11q- phenotype. Through a combination of human genetics and functional studies in genetically engineered mice, the researchers were able to pinpoint ETS-1 as a gene for causing at least a subset of the heart defects that occur in 11q- and the general human population.

Characterized by a distinctive facial appearance, Jacobsen syndrome, also known as 11q terminal deletion disorder (11q-), is a rare resulting from the partial loss of one copy of human chromosome number 11. It is the loss of genes that leads to multiple clinical challenges associated with 11q- such as congenital heart disease, developmental and behavioral problems, low platelet counts, gastrointestinal, urinary and ophthalmologic abnormalities, failure to thrive and slow growth.

"Nearly 15 years ago, in my first month of pediatric cardiology training at UC San Diego, I came across my first patient with 11q-. To this day, I still care for this child," said Grossfeld. "Since then, I have devoted my career to learning everything about this syndrome and hope that we have now more clearly defined the path to understanding, and perhaps preventing, some forms of congenital heart disease."

Related Stories

Recommended for you

Scientists edit gene mutations in inherited form of anemia

October 26, 2016

A Yale-led research team used a new gene editing strategy to correct mutations that cause thalassemia, a form of anemia. Their gene editing technique provided corrections to the mutations and alleviated the disease in mice, ...

Maternal blood test may predict birth complications

October 24, 2016

A protein found in the blood of pregnant women could be used to develop tests to determine the health of their babies and aid decisions on early elective deliveries, according to an early study led by Queen Mary University ...

Scientists find new genetic roots of schizophrenia

October 19, 2016

UCLA scientists have made a major advance in understanding the biology of schizophrenia. Using a recently developed technology for analyzing DNA, the scientists found dozens of genes and two major biological pathways that ...


Please sign in to add a comment. Registration is free, and takes less than a minute. Read more

Click here to reset your password.
Sign in to get notified via email when new comments are made.