Abstract

Here we show that A-kinase anchoring protein 95 (AKAP95) and connexin 43 (Cx43) dynamically interact during cell cycle progression of lung cancer A549 cells. Interaction between AKAP95 and Cx43 at different cell cycle phases was examined by tandem mass spectrometry(MS/MS), confocal immunofluorescence microscopy, Western blot, and co-immunoprecipitation(Co-IP). Over the course of a complete cell cycle, interaction between AKAP95 and Cx43 occurred in two stages: binding stage from late G1 to metaphase, and separating stage from anaphase to late G1. The binding stage was further subdivided into complex binding to DNA in interphase and complex separating from DNA in metaphase. In late G1, Cx43 translocated to the nucleus via AKAP95; in anaphase, Cx43 separated from AKAP95 and aggregated between two daughter nuclei. In telophase, Cx43 aggregated at the membrane of the cleavage furrow. After mitosis, Cx43 was absent from the furrow membrane and was located in the cytoplasm. Binding between AKAP95 and Cx43 was reduced by N-(2-[P-Bromocinnamylamino]-ethyl)-5-isoquinolinesulfonmide (H89) treatment and enhanced by Forskolin. dynamic interaction between AKAP95 and Cx43 varies with cell cycle progression to regulate multiple biological processes.

Highlights

  • A-kinase anchoring protein 95 (AKAP95) is a member of the AKAP family of proteins, which are mainly located in the nucleus of mammalian cells

  • We provide evidence that the interaction between AKAP95 and Connexin 43 (Cx43) is dynamically regulated in lung cancer cells during cell cycle progression

  • 72 proteins involved in cell structural integrity, cell motility, cytokinesis, cell cycle, and apoptosis were identified as Cx43-interacting partners (Fig. 1)

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Summary

Introduction

AKAP95 is a member of the AKAP family of proteins, which are mainly located in the nucleus of mammalian cells. AKAP95 has been shown to form complexes with p68 RNA helicase, RSK1, and MCM2 in the nuclear matrix; these interactions help regulate DNA replication[5,6,7] and maintain mRNA stability[8] in the rat brain. AKAP95 can influence cell cycle progression by binding to cyclins D1-3/E14,12. Cx43 has been shown to interact with multiple proteins, including cadherins, occludin, ZO-1, ZO-2, α -/β -catenins, and CIP75. Through several of these interactions, the phosphorylation state of Cx43 is altered, www.nature.com/scientificreports/. Cx43 reduces Skp[2] expression, inhibits CDK2- and CDK4-mediated phosphorylation of Rb, and regulates cell proliferation by binding cyclin E26

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