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RNA Granules Hitchhike on Lysosomes for Long-Distance Transport, Using Annexin A11 as a Molecular Tether

Ya-Cheng Liao, Michael S. Fernandopulle, Guozhen Wang, Heejun Choi, Ling Hao, Catherine M. Drerup, Rajan Patel, Seema Qamar, Jonathon Nixon‐Abell, Yi Shen, William Meadows, Michele Vendruscolo, Tuomas P. J. Knowles, Matthew P. Nelson, Magdalena A. Czekalska, Greta Musteikytė, Mariam Alexandra Gachechiladze, Christina A. Stephens, Hilda Amalia Pasolli, Lucy R. Forrest, Peter St George‐Hyslop, Jennifer Lippincott‐Schwartz, Michael Emmerson Ward

📄 Abstract

Long-distance RNA transport enables local protein synthesis at metabolically-active sites distant from the nucleus. This process ensures an appropriate spatial organization of proteins, vital to polarized cells such as neurons. Here, we present a mechanism for RNA transport in which RNA granules “hitchhike” on moving lysosomes. In vitro biophysical modeling, live-cell microscopy, and unbiased proximity labeling proteomics reveal that annexin A11 (ANXA11), an RNA granule-associated phosphoinositide-binding protein, acts as a molecular tether between RNA granules and lysosomes. ANXA11 possesses an N-terminal low complexity domain, facilitating its phase separation into membraneless RNA granules, and a C-terminal membrane binding domain, enabling interactions with lysosomes. RNA granule transport requires ANXA11, and amyotrophic lateral sclerosis (ALS)-associated mutations in ANXA11 impair RNA granule transport by disrupting their interactions with lysosomes. Thus, ANXA11 mediates neuronal RNA transport by tethering RNA granules to actively-transported lysosomes, performing a critical cellular function that is disrupted in ALS.

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