A recently discovered genetic regulatory mechanism may shape the immune system's ability to fight viral infections, and play a key role in autoimmune diseases that occur when immune cells attack bodily tissues.
The study published today in Genes and Development by researchers at NYU School of Medicine found that chemical changes to key spots on messenger RNA (mRNA) control the production of interferon beta, which causes inflammation and activates immune cells to destroy viral particles. Specifically, the study shows how a pair of enzymes control production of interferon beta by determining whether or not a methyl group is attached to an adenosine.
Methylation at a specific position on adenosine called N-6 by an enzyme called m6A methyltransferase is counter-balanced by the enzyme ALKBH5, which erases this methylation "mark." The researchers found that this writer/eraser pair, in partnership with other proteins, influenced how much interferon beta mRNA was produced in response to infection with human cytomegalovirus (HCMV), a common infection that begins by injecting its DNA into human cells.
The research team found that interfering with the enzyme that installs the methylation marks at N-6 resulted in greater interferon production, while shutting down the enzyme that removes methyl groups there reduced interferon production.
Importantly, say the authors, the proteins that edit RNA methylation marks were also found to control how much interferon beta was produced by human cells not infected by HMCV, when they sensed that human DNA had escaped from the cell nucleus or mitochondria where it belongs. This can happen when DNA is damaged by chemicals or radiation, or with changes to the structure of the nucleus or mitochondria as cells age.
As misplaced DNA is a known trigger of inflammation in autoimmune and inflammatory diseases, not to mention the aging process, the study mechanisms may represent a newfound treatment approach.
"Our study found that the cellular machinery that controls adenosine methylation on position N-6 plays a fundamental role shaping the immune response of human cells," says senior study author Ian Mohr, Ph.D., a professor in the department of microbiology at NYU Langone Health.