THUMPD2 catalyzesN2-methylation on the spliceosome catalytic center of U6 snRNA and regulates pre-mRNA splicing

Abstract

AbstractHow the relatively evolutionarily conserved spliceosome is able to manage the enormously expanded number of splicing events that occur in humans (∼200,000 vs. ∼400 reported for yeast) is not well understood. Here, we show deposition of one RNA modification-N2-methylguanosine (m2G)-on the G72 nucleoside of U6 snRNA (known to function as the catalytic center of the spliceosome) results in profoundly increased pre-mRNA splicing activity in human cells. This U6 m2G72 modification is conserved among vertebrates. Further, we demonstrate that THUMPD2 is the methyltransferase responsible for U6 m2G72 and show that it interacts with an auxiliary protein (TRMT112) to specifically recognize both sequence and structural elements of U6.THUMPD2KO blocks U6 m2G72 and down-regulates the pre-mRNA splicing activity of major spliceosome, yielding thousands of changed alternative splicing events of endogenous pre-mRNAs. Notably, the aberrantly spliced pre-mRNA population of theTHUMPD2KO cells elicits the nonsense-mediated mRNA decay (NMD) pathway and restricts cell proliferation. Our study thus demonstrates how an RNA epigenetic modification of the major spliceosome differentially regulates global pre-mRNA splicing.