Novel role of PKC ɛ in mitotic spindle stability

Abstract

Mitosis is a highly regulated process characterized by dramatic and coordinated morphological changes to ensure the fidelity of chromosome segregation. Misseg- regation of mitotic chromosomes leads to a condition that underlies chromosomal instability(1), which is a hallmark of cancer. In order to assure symmetry and bipo- larity of the cell division process, mitotic spindle microtubules properly segregate mitotic chromosomes (2). Among the several isoforms of serine/threonine kinases, PKCe is one of the best understood for its role as a transforming oncogene, and it has been found overexpressed in different types of tumors. In 2008, Saurin and col- leagues demonstrated the involvement of PKCe in the regulation of the late stage of mitosis (3). Through its association with 14-3-3 at the midbody, PKCe is essential for the successful completion of cytokinesis, and the inhibition of functional PKCe-14-3- 3 complex leads to abscission failure and multinucleated phenotype in cells. In this study, we found that PKCe is involved in mitotic spindle stability. Using fluorescence microscopy, we found that the active form of PKCe (phosphorylated at Ser-729), co- localizes to the centrosome in cells in metaphase, where the mitotic spindle nuclea- tion occurs. Furthermore, experiments of co-immunoprecipitation revealed that, when cells are synchronized in metaphase, PKCɛ is associated to ɣ-tubulin, a member of the tubulin superfamily localized to the microtubule organizing centers and is essen- tial for microtubule nucleation from centrosomes. Consequently modulation of PKCɛ expression affects spindle stability: PKCɛ downregulation by specific shRNA results in mitotic spindle disorganization with a reduction of the amount of centrosomal and mitotic ɣ-Tubulin and αβ-tubulin fluorescence. Mitotic spindle formation assays using Nocodazole, known to interfere with the polymerization of microtubules, revealed that cells lacking PKCɛ were unable to regrow microtubules after depolymerization. These results reveal a novel role of PKCɛ in mitotic spindle stability, which likely determinant for genome stability.