CDK9 interacts with a RanGTP-NEMP1-Importin β complex to regulate erythroid enucleation
Erythroid enucleation is the final stage of erythroid terminal differentiation and involves the separation of an orthochromatic erythroblast into two daughter cells; a pyrenocyte containing the extruded nucleus, and a reticulocyte that will become a red blood cell. Our previous work identified CDK9 as a regulator of erythroid enucleation that appears to act independently of its known role in regulating RNA polymerase II transcription, suggesting the potential for a new CDK9 role. Using a co-immunoprecipitation and mass spectrometry approach, we identified the interactome of CDK9 in differentiating erythroblasts. We show that CDK9 interacts with a RanGTP-NEMP1-Importin-{beta} complex during erythroid terminal differentiation, and inhibition of importin-{beta} in erythroblasts blocks erythroid enucleation. Using imaging analysis and functional assays of enucleating erythroblasts, we show that CDK9 and importin-{beta} co-locate at a critical site of activity opposite to the nucleus before nuclear extrusion and we describe a novel finding that physically links CDK9 and importin-{beta} activity prior to CaM/Ca2+ signalling and subsequent F-actin activity to achieve enucleation. Key PointsO_LIImportin-{beta} physically interacts with CDK9 in erythroid cells and is a novel regulator of erythroid enucleation C_LIO_LICDK9 and importin-{beta} are required upstream of CaM/Ca2+ signalling to enable nuclear extrusion C_LI