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bioRxiv · 10.1101/2024.12.17.628665

A CRISPR/Cas9 screen reveals proteins at the endosome-Golgi interface that modulate cellular ASO activity

Abstract

Anti-sense oligonucleotides (ASOs) are modified synthetic single-stranded molecules with enhanced stability, activity, and bioavailability. They associate with RNA through sequence complementarity and can reduce or alter mRNA expression upon binding of splice site positions. To target RNA in the nucleus or cytoplasm, ASOs must cross membranes, a poorly understood process. We have performed an unbiased CRISPR/Cas9 knockout screen with a genetic splice reporter to identify genes that can increase or decrease ASOs activity, resulting in the most comprehensive catalog of ASOs-activity modifier genes. Distinct targets were uncovered, including AP1M1 and TBC1D23, linking ASOs activity to transport of cargo between the Golgi and endosomes. AP1M1 absence strongly increased ASO activity by delaying endosome-to-lysosome transport in vitro and in vivo. Prolonged ASOs residence time in the endosomal system may increase the likelihood of ASOs escape from this organelle before they reach lysosomes. This insight into AP1M1 role in ASOs trafficking suggests a way for enhancing the therapeutic efficacy of ASOs by manipulating the endolysosomal pathways.

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BibTeXRIS

Malong, L., Roskosch, J., Hager, C., Fortin, J.-P., Schmucki, R., Callow, M. G., Weile, C., Romeo, V., Patsch, C., Martin, S., Costa, M., Modrusan, Z., Villasenor, R., Koller, E., Haley, B., Spang, A., Roudnicky, F.. 2024-12-18. A CRISPR/Cas9 screen reveals proteins at the endosome-Golgi interface that modulate cellular ASO activity. https://doi.org/10.1101/2024.12.17.628665

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