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bioRxiv · 10.1101/2021.05.24.445478

HIV-1 Nef and CycK:CDK13 antagonize SERINC5 for optimal viral infectivity

Chai, Q.·Li, S.·Collins, M. K.·Li, R.·Ahmad, I.·Johnson, S. F.·Frabutt, D. A.·Yang, Z.·Shen, X.·Sun, L.·Hu, J.·Hultquist, J. F.·Peterlin, B. M.·Zheng, Y.-H.
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Abstract

HIV-1 Nef antagonizes SERINC5 by redirecting this potent restriction factor to the endosomes and lysosomes for degradation. However, the precise mechanism remains unclear. Using affinity purification/mass spectrometry, we identified cyclin K and cyclin-dependent kinase 13 (CycK:CDK13) as a new Nef-associated kinase complex. CycK:CDK13 phosphorylates the serine at position 360 (S360) in SERINC5, which is required for Nef downregulation of SERINC5 from the cell surface and its counter activity of the SERINC5 antiviral activity. To understand the role of S360 phosphorylation, we created chimeric proteins between CD8 and SERINC5. Nef not only downregulates, but importantly, also binds to this chimera in a S360-dependent manner. Thus, S360 phosphorylation increases interactions between Nef and SERINC5 and initiates the destruction of SERINC5 by the endocytic machinery.

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Chai, Q., Li, S., Collins, M. K., Li, R., Ahmad, I., Johnson, S. F., Frabutt, D. A., Yang, Z., Shen, X., Sun, L., Hu, J., Hultquist, J. F., Peterlin, B. M., Zheng, Y.-H.. 2021-05-24. HIV-1 Nef and CycK:CDK13 antagonize SERINC5 for optimal viral infectivity. https://doi.org/10.1101/2021.05.24.445478

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