| Literature DB >> 32433973 |
Laurensia Yuniati1, Angela Lauriola2, Manouk Gerritsen1, Susana Abreu1, Eric Ni3, Chiara Tesoriero2, Jacob O Onireti2, Teck Yew Low4, Albert J R Heck5, Andrea Vettori2, Timothy Cardozo3, Daniele Guardavaccaro6.
Abstract
Cullin-RING ligases (CRLs) control key cellular processes by promoting ubiquitylation of a multitude of soluble cytosolic and nuclear proteins. Subsets of CRL complexes are recruited and activated locally at cellular membranes; however, few CRL functions and substrates at these distinct cellular compartments are known. Here, we use a proteomic screen to identify proteins that are ubiquitylated at cellular membranes and found that Lunapark, an endoplasmic reticulum (ER)-shaping protein localized to ER three-way junctions, is ubiquitylated by the CRL3KLHL12 ubiquitin ligase. We demonstrate that Lunapark interacts with mechanistic target of rapamycin complex-1 (mTORC1), a central cellular regulator that coordinates growth and metabolism with environmental conditions. We show that mTORC1 binds Lunapark specifically at three-way junctions, and lysosomes, where mTORC1 is activated, make contact with three-way junctions where Lunapark resides. Inhibition of Lunapark ubiquitylation results in neurodevelopmental defects indicating that KLHL12-dependent ubiquitylation of Lunapark is required for normal growth and development.Entities:
Keywords: ER three-way junction; Lunapark; cullin-RING ligases; endoplasmic reticulum; lysosome; mTORC1; ubiquitin
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Year: 2020 PMID: 32433973 DOI: 10.1016/j.celrep.2020.107664
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423