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bioRxiv · 10.1101/2020.07.20.213066

Regulated assembly of the ER membrane protein complex

Pleiner, T.·Januszyk, K.·Tomaleri, G. P.·Oania, R. S.·Hazu, M.·Sweredoski, M. J.·Moradian, A.·Guna, A.·Voorhees, R. M.
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Abstract

The assembly of nascent proteins into multi-subunit complexes is tightly regulated to maintain cellular homeostasis. The ER membrane protein complex (EMC) is an essential insertase that requires seven membrane-spanning and two soluble subunits for function. Here we show that the kinase With no lysine 1 (WNK1), known for its role in hypertension and neuropathy, is required for assembly of the human EMC. WNK1 uses a conserved amphipathic helix to stabilize the soluble subunit, EMC2, by binding to the EMC2-8 interface. Shielding this hydrophobic surface prevents promiscuous interactions of unassembled EMC2 and precludes binding of ubiquitin ligases, permitting assembly. Using biochemical reconstitution, we show that after EMC2 reaches the membrane, its interaction partners within the EMC displace WNK1, and similarly shield its exposed hydrophobic surfaces. This work describes an unexpected role for WNK1 in protein biogenesis, and defines the general requirements of an assembly factor that will apply across the proteome.

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Pleiner, T., Januszyk, K., Tomaleri, G. P., Oania, R. S., Hazu, M., Sweredoski, M. J., Moradian, A., Guna, A., Voorhees, R. M.. 2020-07-21. Regulated assembly of the ER membrane protein complex. https://doi.org/10.1101/2020.07.20.213066

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