In a study published in iScience, Professor Akiyoshi Fukamizu of the Life Science Center for Survival Dynamics, Tsukuba Advanced Research Alliance (University of Tsukuba, JAPAN) and the research group reported a new work on discovery of the important role of PRMT1 in dilated cardiomyopathy(DCM).
The heart pumps blood to all organs and tissues of our body that need the oxygen and nutrients it carries. In the United States, the mortality rate due to cardiomyopathies is greater than 10,000 deaths per year. On the other hand, in one of the most common types of heart disease, DCM, the heart (cardiac) muscle enlarges and weakens, preventing the heart from pumping blood efficiently. Moreover, at the time of listing for heart transplantation, the median age is 4years (Ref. 1), and approximately over 10% of children affected with DCM have died at age 2(Ref. 2). While it is known that mutations in the alternative splicing regulator RBM20 gene have been shown to cause human DCM(Ref. 3), genetic information such as gene expression and alternative splicing related to DCMs remains unidentified.
Arginine methylation is a posttranslational modification of proteins, and is catalyzed by protein arginine methyltransferases (PRMTs). PRMT1, amajormethyltransferase active in mammalian cells, regulates various cellular functions such as gene expression, DNA replication, and cell proliferation. It is of note that these functions were identified by experiments with culture cells, while physiological roles of arginine methylation have been largely unknown.
Previous studies showed the expression levels of PRMT1 were changed in the heart tissue of heart failure patients. However, we did not understand the role of PRMT1 in the normal or the failing heart. To address this question, researchers generated heart-specific PRMT1 knockout mouse, namely PRMT1-cKO mouse, which lacks PRMT1 in cardiomyocytes, the heart muscles. Interestingly, the PRMT1-cKO mice developed severe DCM from the juvenile stage and sudden death, suggesting that PRMT1 is critical for the proper cardiac function.
To uncover the mechanism underlying the heart dysfunction in PRMT1-cKO mice, the researchers focused on messenger RNA (mRNA) alternative splicing, because some splicing regulators were known as methylation targets of PRMT1. Alternative splicing is a cellular system that produces a variety of proteins from a genome by selecting which part of the genes should be translated to proteins. Using a high-throughput RNA sequencing (RNA-seq) for gene analysis, researchers found aberrant mRNA splicing patterns of multiple genes in the PRMT1-deficient heart, suggesting that dysregulation of alternative splicing is strongly linked to the defective cardiac function observed in PRMT1-cKO mice.
Recently, a number of studies have suggested that abnormal mRNA splicing is related to the pathogenesis of DCM; however, its regulatory mechanisms are largely unknown. “Our findings may become a breakthrough for understanding the mechanism of DCM,” says Akiyoshi Fukamizu. “DCM has serious prognosis, especially in cases of patients at young ages, including infants. We hope our study will benefit the development of new treatments for DCM patients.”