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

Authors
Liao YC1, Fernandopulle MS2, Wang G3, Choi H1, Hao L2, Drerup CM4, Patel R2, Qamar S3, Nixon-Abell J3, Shen Y5, Meadows W3, Vendruscolo M5, Knowles TPJ6, Nelson M2, Czekalska MA5, Musteikyte G5, Gachechiladze MA2, Stephens CA2, Pasolli HA1, Forrest LR2, St George-Hyslop P7, Lippincott-Schwartz J8, Ward ME9.
10-16-2019 HSW 1057
12:00pm
PST
Categories
RNA Transport & Localization
Speaker
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.