Our programmable mRNA medicines called Omega Epigenomic Controllers (OECs) leverage nature’s innate mechanism for gene regulation and epigenetically tune dysregulated genes back to normal levels of expression.
What are OECs?
OECs are mRNA-based therapeutics that are programmed to target unique sequences within the genome with high specificity to controllably tune gene expression for a tailored duration, allowing for options beyond just “all on” or “all off.” By acting pre-transcriptionally at the highest level of gene regulation, OECs are designed to overcome the compensatory autoregulation often associated with key disease drivers, including those historically undruggable with conventional approaches.
How Do OECs Work?
Our initial OEC programs leverage lipid-nanoparticle (LNP) technology. When delivered as LNPs, OECs are taken up by cells where the mRNA cargo is translated into therapeutic protein by the cell’s natural machinery.
The mRNA expresses a fusion protein comprised of a highly specific DNA-binding domain and an epigenomic effector capable of controlling the various regulators of gene expression by leveraging a broad set of epigenetic mechanisms, such as DNA methylation/demethylation and those controlling the state of chromatin (e.g., histone modification, acetylation, etc.).
Following translation, the proteins enter the cell nucleus and home into the target IGD, where they make the appropriate epigenetic modifications at the specified Epigenomic Zipcode, or EpiZip™. The mRNA and expressed proteins are degraded within a few days by normal cellular processes, while the programmed epigenetic modification(s) can persist for either days, weeks, or months, depending on the duration engineered into the OEC by virtue of the target and effector domains. Since this approach preserves native nucleic acid sequences, it may eliminate the safety concerns associated with other treatment modalities that modify the genome.