NAK-associated protein 1/NAP1 activates TBK1 to ensure accurate mitosis and cytokinesis

Author:

Paul Swagatika1ORCID,Sarraf Shireen A.2ORCID,Nam Ki Hong3ORCID,Zavar Leila4ORCID,DeFoor Nicole4ORCID,Biswas Sahitya Ranjan5ORCID,Fritsch Lauren E.5ORCID,Yaron Tomer M.67ORCID,Johnson Jared L.6ORCID,Huntsman Emily M.67ORCID,Cantley Lewis C.689ORCID,Ordureau Alban3ORCID,Pickrell Alicia M.4ORCID

Affiliation:

1. Virginia-Maryland College of Veterinary Medicine 1 Graduate Program in Biomedical and Veterinary Sciences, , Blacksburg, VA, USA

2. National Institutes of Neurological Disorders and Stroke, National Institutes of Health 2 Biochemistry Section, , Bethesda, MD, USA

3. Sloan Kettering Institute, Memorial Sloan Kettering Cancer Center 3 Cell Biology Program, , New York, NY, USA

4. Virginia Polytechnic Institute and State University 4 School of Neuroscience, , Blacksburg, VA, USA

5. Virginia Polytechnic Institute and State University 5 Translational Biology, Medicine, and Health Graduate Program, , Roanoke, VA, USA

6. Weill Cornell Medicine 6 Meyer Cancer Center, , New York, NY, USA

7. Weill Cornell Medicine 7 Englander Institute for Precision Medicine, Institute for Computational Biomedicine, , New York, NY, USA

8. Harvard Medical School 8 Department of Cell Biology, , Boston, MA, USA

9. Harvard Medical School 9 Dana-Farber Cancer Institute, , Boston, MA, USA

Abstract

Subcellular location and activation of Tank Binding Kinase 1 (TBK1) govern precise progression through mitosis. Either loss of activated TBK1 or its sequestration from the centrosomes causes errors in mitosis and growth defects. Yet, what regulates its recruitment and activation on the centrosomes is unknown. We identified that NAK-associated protein 1 (NAP1) is essential for mitosis, binding to and activating TBK1, which both localize to centrosomes. Loss of NAP1 causes several mitotic and cytokinetic defects due to inactivation of TBK1. Our quantitative phosphoproteomics identified numerous TBK1 substrates that are not only confined to the centrosomes but are also associated with microtubules. Substrate motifs analysis indicates that TBK1 acts upstream of other essential cell cycle kinases like Aurora and PAK kinases. We also identified NAP1 as a TBK1 substrate phosphorylating NAP1 at S318 to promote its degradation by the ubiquitin proteasomal system. These data uncover an important distinct function for the NAP1–TBK1 complex during cell division.

Funder

National Institutes of Health

Publisher

Rockefeller University Press

Subject

Cell Biology

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