New Gene Linked to Congenital Heart Defects

Key points
- 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.
- “Identification of this gene may have implications for prevention of some of these most common types of congential heart defects,” said Paul Grossfeld, MD, 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.
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 congential heart defects,” said Paul Grossfeld, MD, 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 chromosomal disorder 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.”
This research was funded by grants from the National Institutes of Health, the State of South Dakota, and the Children’s Heart Institute Fund from Rady Children’s Hospital-San Diego.
Researchers involved in this study include Maoqing Ye, UC San Diego; Chris Coldren, University of Colorado Health Sciences Center; Xingqun Liang, UC San Diego, Teresa Mattina, University of Catania; Elizabeth Goldmuntz, Children's Hospital of Philadelphia; D Woodrow Benson, Cincinnati Children's Hospital; Dunbar Ivy, University of Colorado Health Sciences Center; MB Perryman, University of South Dakota; Lee Ann Garrett-Sinha, SUNY-Buffalo; and Paul Grossfeld, UC San Diego.
Source: University of California, San Diego Health Sciences
Written and revised by
Gerald Hurowitz, M.D.
Our doctors write and review articles for accuracy and keep them up to date.
health.am provides general information, not medical advice. Always consult a qualified health professional about your own health.
Explore health topics
More in this topic
Heart & Blood Vessels →
NewsLong-lasting gene therapy benefits advanced heart failure patients
Researchers from the Cardiovascular Research Center at Icahn School of Medicine at Mount Sinai reported the long-term benefits of a single dose of their gene therapy AAV1/SERCA2a in advanced heart failure patients on…
20 November 2013
NewsTV watching linked to young adults' heart risk
Watching a favorite television show may feel relaxing, but in a new study, the longer 30-somethings spent in front of the TV, the stiffer their arteries - a sign of likely heart disease in the future. "The fact that…
16 October 2013
NewsCalcium Linked to Increased Risk of Heart Disease and Death in Patients With Kidney Disease
Kidney patients who take calcium supplements to lower their phosphorus levels may be at a 22 per cent higher risk of death than those who take other non-calcium based treatments, according to a new study by Women's…



