TY - JOUR
T1 - Multifunctional human transcriptional coactivator protein PC4 is a substrate of Aurora kinases and activates the Aurora enzymes
AU - Dhanasekaran, Karthigeyan
AU - Kumari, Sujata
AU - Boopathi, Ramachandran
AU - Shima, Hiroki
AU - Swaminathan, Amrutha
AU - Bachu, Mahesh
AU - Ranga, Udaykumar
AU - Igarashi, Kazuhiko
AU - Kundu, Tapas K.
N1 - Publisher Copyright:
© 2016 Federation of European Biochemical Societies.
Copyright:
Copyright 2017 Elsevier B.V., All rights reserved.
PY - 2016/3/1
Y1 - 2016/3/1
N2 - Positive coactivator 4 (PC4), a human transcriptional coactivator, is involved in diverse processes like chromatin organization and transcription regulation. It is hyperphosphorylated during mitosis, with unknown significance. For the first time, we demonstrate the function of PC4 outside the nucleus upon nuclear envelope breakdown. A fraction of PC4 associates with Aurora A and Aurora B and undergoes phosphorylation, following which PC4 activates both Aurora A and B to sustain optimal kinase activity to maintain the phosphorylation gradient for the proper functioning of the mitotic machinery. This mitotic role is evident in PC4 knockdown cells where the defects are rescued only by the catalytically active Aurora kinases, but not the kinase-dead mutants. Similarly, the PC4 phosphodeficient mutant failed to rescue such defects. Hence, our observations establish a novel mitotic function of PC4 that might be dependent on Aurora kinase-mediated phosphorylation.
AB - Positive coactivator 4 (PC4), a human transcriptional coactivator, is involved in diverse processes like chromatin organization and transcription regulation. It is hyperphosphorylated during mitosis, with unknown significance. For the first time, we demonstrate the function of PC4 outside the nucleus upon nuclear envelope breakdown. A fraction of PC4 associates with Aurora A and Aurora B and undergoes phosphorylation, following which PC4 activates both Aurora A and B to sustain optimal kinase activity to maintain the phosphorylation gradient for the proper functioning of the mitotic machinery. This mitotic role is evident in PC4 knockdown cells where the defects are rescued only by the catalytically active Aurora kinases, but not the kinase-dead mutants. Similarly, the PC4 phosphodeficient mutant failed to rescue such defects. Hence, our observations establish a novel mitotic function of PC4 that might be dependent on Aurora kinase-mediated phosphorylation.
KW - Aurora kinase
KW - cell cycle
KW - cytokinesis
KW - positive coactivator 4
KW - spindle organization
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U2 - 10.1111/febs.13653
DO - 10.1111/febs.13653
M3 - Review article
C2 - 26777301
AN - SCOPUS:84975709014
VL - 283
SP - 968
EP - 985
JO - FEBS Journal
JF - FEBS Journal
SN - 1742-464X
IS - 6
ER -