Cho, Yena Hwang, Jee Won Bedford, Mark T. Song, Dae-Geun Kim, Su Nam Kim, Yong Kee 2025-03-21T08:00:08Z 2025-03-21T08:00:08Z 2025-03-19 2025-03 1478-811X https://pubs.kist.re.kr/handle/201004/151950 Tubulin is crucial in several cellular processes, including intracellular organization, organelle transport, motility, and chromosome segregation. Intracellular tubulin concentration is tightly regulated by an autoregulation mechanism, in which excess free tubulin promotes tubulin mRNA degradation. However, the details of how changes in free tubulin levels initiate this autoregulation remain unclear. In this study, we identified coactivator-associated arginine methyltransferase 1 (CARM1)-phosphatidylinositol 3-kinase class 2 alpha (PI3KC2 alpha) axis as a novel regulator of tubulin autoregulation. CARM1 stabilizes PI3KC2 alpha by methylating its R175 residue. Once PI3KC2 alpha is not methylated, it becomes unstable, leading to decreased cellular levels. Loss of PI3KC2 alpha results in the release of tetratricopeptide repeat domain 5 (TTC5), which initiates tubulin autoregulation. Thus, PI3KC2 alpha, along with its CARM1-mediated arginine methylation, regulates the initiation of tubulin autoregulation. Additionally, disruption of the CARM1-PI3KC2 alpha axis decreases intracellular tubulin levels, leading to a synergistic increase in the cytotoxicity of microtubule-targeting agents (MTAs). Taken together, our study demonstrates that the CARM1-PI3KC2 alpha axis is a key regulator of TTC5-mediated tubulin autoregulation and that disrupting this axis enhances the anti-cancer activity of MTAs. English BioMed Central CARM1 regulates tubulin autoregulation through PI3KC2α R175 methylation Article 10.1186/s12964-025-02124-z 1 Cell Communication and Signaling, v.23, no.1 Cell Communication and Signaling 23 1 Y scie scopus 001439165100002 2-s2.0-86000096767 Cell Biology Cell Biology Article PI3K-C2-ALPHA MICROTUBULES DEGRADATION ENDOCYTOSIS PI3K 3-KINASE CARM1 PI3KC2 alpha Tubulin Autoregulation Mitosis