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A promising target for new RNA therapeutics now accessible

A promising target for new RNA therapeutics now accessible
Newly developed inhibitor (green) prevents METTL16 (purple) from interaction with target RNA (turquois) and thus inhibits the transfer of the methyl group (Me). Credit: MPI of Molecular Physiology

Only recently, a new era in medicine began with the first RNA vaccines. These active substances are modified RNAs that trigger immune responses of the human immune system. Another approach in RNA medicine targets the body's own RNA and its protein modulators by specifically tailored active substances.

Scientists around Peng Wu, research group leader at the Chemical Genomics Center at the Max Planck Institute of Molecular Physiology in Dortmund, have now developed the first small-molecule inhibitors against the RNA-modifying enzyme METTL16. The methyltransferase is responsible for the regulation of different RNAs and is a promising anti-cancer target.

The new findings lay the foundation for a comprehensive investigation of the role of METTL16 in health and disease and are a step closer towards the development of therapeutic agents targeting such RNA modifiers. The research is published in the journal JACS Au.

RNA has long been considered only as a passive messenger in the cell, produced by DNA transcription to transfer genetic information to the protein factories, the ribosomes. However, it has turned out, that RNA does much more than that. In addition to the coding DNA just described, there is also non-coding DNA controlling many by regulating the activity of genes at many levels. No less than a dozen RNA classes have been identified. RNAi for example, is used by the cell to degrade particular RNA targets to silence genes, when it comes to fighting foreign viral DNA.

Readers, writers, and erasers

RNA interacts with a plethora of biomolecules, not only other RNAs or DNA but also proteins and metabolites. The resulting regulatory complexes control diverse vital cellular processes and errors can cause diseases. RNA's fate is determined by chemical modifications that affect its stability, structure and interactions and thereby its fate.

More than 170 distinct RNA modifications have been described thus far. The most abundant is the methylation on the N6-position of the RNA-nucleotide adenosine (m6A). It allows the cell to quickly respond to environmental changes by initiating appropriate cellular responses, such as division, differentiation or migration.

This is why RNA-methylation needs to be tightly controlled, taken care of by a set of proteins: "writers" deposit, "readers" recognize and "erasers" remove the .

New substance prevents writing to RNA

Aberrant RNA methylation has been associated with cancers and other human diseases, making "writers" an attractive therapeutic target. Only a handful of RNA m6A writers have been identified so far. And only for one of them, METTL3, potent inhibitors have been reported. These molecules prevent the writer from absorbing the ink, the biomolecule S-adenosyl methionine (SAM).

The group of Peng Wu has now identified the first inhibitor of the writer METTL16. However, in contrast to the before-mentioned inhibitors, it showed a different mode of action: it prevents the interaction of METTL16 with RNA. The scientists were able to identify this new type of inhibitor by developing an assay evaluating the disruption between METTL16 and a fluorophore-labeled mRNA substrate.

"Certain have elevated writer levels and are also more vulnerable to reduction of SAM levels, which makes them promising anticancer targets. However, the exact biological consequences of METTL16's binding to RNA substrates are not yet clearly determined. With our work, we lay the foundation for a better investigation of the role of METTL16 in disease and health, but also for the development of novel RNA-targeting therapeutics," says Peng Wu.

More information: Yang Liu et al, Aminothiazolone Inhibitors Disrupt the Protein–RNA Interaction of METTL16 and Modulate the m6A RNA Modification, JACS Au (2024). DOI: 10.1021/jacsau.3c00832

Provided by Max Planck Society

Citation: A promising target for new RNA therapeutics now accessible (2024, April 10) retrieved 25 May 2024 from
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