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bioRxiv · 10.1101/2023.06.21.545957

Functional interaction of torsinA and its activators in liver lipid metabolism

Abstract

TorsinA is an atypical ATPase that lacks intrinsic activity unless it is bound to its activators lamina-associated polypeptide 1 (LAP1) in the perinuclear space or luminal domain-like LAP1 (LULL1) throughout the endoplasmic reticulum. However, the interaction of torsinA with LAP1 and LULL1 has not yet been shown to modulate a defined physiological process in mammals in vivo. We previously demonstrated that depletion of torsinA from mouse hepatocytes leads to reduced liver triglyceride secretion and marked steatosis, whereas depletion of LAP1 had more modest similar effects. We now show that depletion of LULL1 alone does not significantly decrease liver triglyceride secretion or cause steatosis. However, simultaneous depletion of both LAP1 and LULL1 from hepatocytes leads to defective triglyceride secretion and marked steatosis similar to that observed with depletion of torsinA. Our results demonstrate that torsinA and its activators dynamically regulate a physiological process in mammals in vivo.

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BibTeXRIS

Hernandez-Ono, A., Zhao, Y. P., Murray, J. M., Ostlund, C. A., Lee, M. J., Ginsberg, H. N., Worman, H. J., Shin, J.-Y.. 2023-06-22. Functional interaction of torsinA and its activators in liver lipid metabolism. https://doi.org/10.1101/2023.06.21.545957

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