Study Supports Link Between SORBS2 and Congenital Heart Disease

Study Supports Link Between SORBS2 and Congenital Heart Disease
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New data on how the SORBS2 gene may cause congenital heart disease (CHD) has been published this week in eLife. The researchers showed that knockdown of SORBS2, a 4q interval gene, disrupted sarcomeric integrity of cardiomyocytes and caused reduced cardiomyocyte number in a human embryonic stem cell differentiation model. Their findings indicate that SORBS2 is a regulator of secondary heart field (SHF) development and the gene’s variants contribute to CHD pathogenesis.

Previous studies have linked heart defects related to chromosome 4q deletion syndrome to a missing copy of the HAND2 gene, which is found on that chromosome and is important for heart development. But not every patient with a congenital heart defect is missing HAND2, suggesting other genes are likely involved as well.

“A previous study of one patient with congenital heart disease suggested mutations in a gene called SORBS2 might be responsible, but this finding had yet to be confirmed,” explains first author Fei Liang, a physician at the Neonatal Intensive Care Unit, Shanghai Children’s Medical Center, China.

Chromosome 4q deletion is one of the most frequently detected genomic imbalance events in CHD patients. Those patients have a spectrum of clinical manifestations including craniofacial, cardiovascular, and gastrointestinal abnormalities, and mental and growth deficiencies. A previous study narrowed the cardiovascular critical region to 4q32.2–q34.3, which contains TLL1HPGD, and HAND2 genes.

To explore the potential role of SORBS2 in congenital heart disease, Liang and colleagues suppressed the gene in developing human heart cells grown in the laboratory. This led to the development of abnormally shaped heart cells and interfered with the ability of cardiac muscle cells to undergo necessary changes in gene expression.

Molecular analyses revealed decreased expression of SHF marker genes and impaired NOTCH and SHH signaling in SORBS2-knockdown cells. Exogenous SHH rescued SORBS2 knockdown-induced cardiomyocyte differentiation defects.

Additional studies in genetically engineered mice showed that a lack of SORBS2 led to the absence or duplication of the wall between the two upper chambers of the heart in 40% of embryos. This duplication is a condition known as double atrial septum. However, the effect was much milder in comparison to human heart defects, suggesting that SORBS2 may be a ‘small effect size’ congenital heart disease gene – that is to say, it plays a minor role in the disease.

The team further examined how a lack of SORBS2 can affect gene expression in both mice and human cells. Their results highlighted how the levels of other genes and proteins are elevated or reduced in response to the lack of SORBS2, ultimately leading to heart defects and damage.

Finally, the teams found that rare, damaging variants of the SORBS2 gene were significantly enriched in 300 congenital heart disease cases where gross chromosomal aberrations did not occur. This provides additional genetic evidence that SORBS2 variants have a role in causing general congenital heart disease.

“Our combined studies help explain the cause of congenital heart disease in chromosome 4q deletion syndrome patients who still have the functional HAND2 gene,” said senior author Zhen Zhang, a professor at Shanghai Pediatric Congenital Heart Disease Institute and Pediatric Translational Medicine Institute, Shanghai Children’s Medical Center.

“They provide an effective approach for identifying other genes that play a minor role in congenital heart disease and other multigenic diseases. Interestingly, we found that SORBS2 deficiency can cause double atrial septum, a very rare cardiac anomaly linked to a condition called paradoxical thromboembolism. The exact causes of this anomaly are currently unknown, and we hope our study paves the way for exploring this further.”