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A kinase-independent function for AURORA-A in replisome assembly during DNA replication initiation.

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Guarino Almeida, Estrella 
Renaudin, Xavier 
Venkitaraman, Ashok R 


The catalytic activity of human AURORA-A kinase (AURKA) regulates mitotic progression, and its frequent overexpression in major forms of epithelial cancer is associated with aneuploidy and carcinogenesis. Here, we report an unexpected, kinase-independent function for AURKA in DNA replication initiation whose inhibition through a class of allosteric inhibitors opens avenues for cancer therapy. We show that genetic depletion of AURKA, or its inhibition by allosteric but not catalytic inhibitors, blocks the G1-S cell cycle transition. A catalytically inactive AURKA mutant suffices to overcome this block. We identify a multiprotein complex between AURKA and the replisome components MCM7, WDHD1 and POLD1 formed during G1, and demonstrate that allosteric but not catalytic inhibitors prevent the chromatin assembly of functional replisomes. Indeed, allosteric but not catalytic AURKA inhibitors sensitize cancer cells to inhibition of the CDC7 kinase subunit of the replication-initiating factor DDK. Thus, our findings define a mechanism essential for replisome assembly during DNA replication initiation that is vulnerable to inhibition as combination therapy in cancer.



Allosteric Regulation, Aurora Kinase A, Cell Cycle Checkpoints, Cell Cycle Proteins, Cell Line, DNA Replication, DNA-Directed DNA Polymerase, G1 Phase Cell Cycle Checkpoints, HeLa Cells, Humans, Interphase, Multienzyme Complexes, Protein Kinase Inhibitors, Protein Serine-Threonine Kinases, Replication Origin

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Nucleic Acids Res

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Oxford University Press (OUP)
Medical Research Council (MC_UU_12022/1)
MRC (MC_UU_12022/8)
Wellcome Trust (101134/Z/13/Z)