Abstract

Connexin 43 (Cx43) is a gap junction protein that assembles at the cell border to form intercellular gap junction (GJ) channels which allow for cell–cell communication by facilitating the rapid transmission of ions and other small molecules between adjacent cells. Non-canonical roles of Cx43, and specifically its C-terminal domain, have been identified in the regulation of Cx43 trafficking, mitochondrial preconditioning, cell proliferation, and tumor formation, yet the mechanisms are still being explored. It was recently identified that up to six truncated isoforms of Cx43 are endogenously produced via alternative translation from internal start codons in addition to full length Cx43, all from the same mRNA produced by the gene GJA1. GJA1-11k, the 11kDa alternatively translated isoform of Cx43, does not have a known role in the formation of gap junction channels, and little is known about its function. Here, we report that over expressed GJA1-11k, unlike the other five truncated isoforms, preferentially localizes to the nucleus in HEK293FT cells and suppresses cell growth by limiting cell cycle progression from the G0/G1 phase to the S phase. Furthermore, these functions are independent of the channel-forming full-length Cx43 isoform. Understanding the apparently unique role of GJA1-11k and its generation in cell cycle regulation may uncover a new target for affecting cell growth in multiple disease models.

Highlights

  • Gap Junction (GJ) channels are formed by connexin proteins, which assemble as hexamers on the cell membrane and dock with the hexamer in an adjacent cell, creating a channel for intercellular communication [1]

  • We explored the effect of the full length Connexin 43 (Cx43) and the GJA1-11k isoforms on cell proliferation

  • We explored the stage at which cell growth is inhibited by GJA1-11k in the nucleus

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Summary

Introduction

Gap Junction (GJ) channels are formed by connexin proteins, which assemble as hexamers on the cell membrane and dock with the hexamer in an adjacent cell, creating a channel for intercellular communication [1]. Connexin 43 (Cx43) is the most prevalent gap junction protein in the heart and is widely expressed in most mammalian organs and cell types [2]. Studies have identified numerous non-canonical roles of Cx43 that are not described by gap junction channel activity, including in ischemic injury protection [4,5], cancer [6,7,8,9], wound healing [10], muscle differentiation [11], organ morphogenesis [12,13], and cell migration in embryonic development [14]. Few studies have been able to reconcile how the gap junction Cx43 channel function can influence these apparently channel-independent roles of Cx43 protein

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