An Alternatively Translated Connexin 43 Isoform, GJA1-11k, Localizes to the Nucleus and Can Inhibit Cell Cycle Progression

• Published in: Biomolecules (Basel, Switzerland) Switzerland), 2020-03, Vol.10 (3), p.473
• Main Authors: Epifantseva, Irina, Xiao, Shaohua, Baum, Rachel E, Kléber, André G, Hong, TingTing, Shaw, Robin M
• Format: Article
• Language: English
• Subjects: Cell adhesion & migration; Cell Cycle; Cell growth; Cell interactions; Cell Nucleus - genetics; Cell Nucleus - metabolism; Cell proliferation; Cell signaling; Cloning; Codons; Connexin 43; Connexin 43 - biosynthesis; Connexin 43 - genetics; connexin43; Cytomegalovirus; G1 phase; Gap junctions; HEK293 Cells; Humans; Immunoglobulins; internal translation; Isoforms; Mitochondria; mRNA; Mutagenesis; Observations; Physiological aspects; Plasmids; Protein Biosynthesis; Protein expression; Protein Isoforms - biosynthesis; Protein Isoforms - genetics; Proteins; S phase; trafficking; Tumors
• ISSN: 2218-273X; 2218-273X
• DOI: 10.3390/biom10030473

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 . GJA1-11k, 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 G /G 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.