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

被引:1
|
作者
Paul, Swagatika [1 ]
Sarraf, Shireen A. [2 ]
Nam, Ki Hong [3 ]
Zavar, Leila [4 ]
Defoor, Nicole [4 ]
Biswas, Sahitya Ranjan [5 ]
Fritsch, Lauren E. [5 ]
Yaron, Tomer M. [6 ]
Johnson, Jared L. [6 ]
Huntsman, Emily M. [6 ,7 ]
Cantley, Lewis C. [6 ,8 ,9 ]
Ordureau, Alban [3 ]
Pickrell, Alicia M. [4 ]
机构
[1] Virginia Maryland Coll Vet Med, Grad Program Biomed & Vet Sci, Blacksburg, VA USA
[2] NINDS, Biochem Sect, NIH, Bethesda, MD USA
[3] Mem Sloan Kettering Canc Ctr, Cell Biol Program, Sloan Kettering Inst, New York, NY USA
[4] Virginia Polytech Inst & State Univ, Sch Neurosci, Blacksburg, VA 24061 USA
[5] Virginia Polytech Inst & State Univ, Translat Biol Med & Hlth Grad Program, Roanoke, VA USA
[6] Weill Cornell Med, Meyer Canc Ctr, New York, NY USA
[7] Weill Cornell Med, Englander Inst Precis Med, Inst Computat Biomed, New York, NY USA
[8] Harvard Med Sch, Dept Cell Biol, Boston, MA USA
[9] Harvard Med Sch, Dana Farber Canc Inst, Boston, MA USA
来源
JOURNAL OF CELL BIOLOGY | 2023年 / 223卷 / 02期
基金
美国国家卫生研究院;
关键词
BINDING KINASE 1; AUTOPHAGY RECEPTOR; CELL-CYCLE; PHOSPHORYLATION ANALYSIS; DAMAGED MITOCHONDRIA; CROSS-TALK; G1; PHASE; OPTINEURIN; RECRUITMENT; AURORA;
D O I
10.1083/jcb.202303082
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Paul et al. demonstrate that NAP1/AZI2 is a cell cycle protein that activates TBK1 during mitosis and regulates key mitotic and cytokinetic proteins to ensure accurate cell division. 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.
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页数:31
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