# Stability of c-Myc Protein in Early S Phase Is Regulated by the Interaction with PCNA

## TL;DR

The c-Myc protein's stability in early DNA replication is controlled by its interaction with PCNA and the CRL4 complex.

## Contribution

Discovery of a functional link between c-Myc, PCNA, and the CRL4 complex in regulating protein stability during DNA replication.

## Key findings

- c-Myc interacts with PCNA via a PIP box motif in early S-phase cells.
- c-Myc interacts with CUL4A and DDB1, components of the CRL4 complex.
- Disrupting the PIP box or depleting CUL4A increases c-Myc protein stability.

## Abstract

The transcription factor c-Myc is known to regulate DNA replication via a non-transcriptional mechanism by interacting with proteins of the pre-replicative complex. In addition, c-Myc localizes to DNA replication foci, similarly to Proliferating Cell Nuclear Antigen (PCNA); however, the significance of this localization remains unclear. Here, we investigated whether c-Myc interacts with PCNA and analyzed the possible function of this association. We found a conserved interaction motif, the PCNA-interacting protein (PIP) box, in the N-terminal region of c-Myc. Confocal microscopy analysis showed co-localization with PCNA in early S-phase, but not in late S-phase cells. Co-immunoprecipitation from cell extracts and pull-down of recombinant proteins indicated a direct physical association between c-Myc and PCNA, which was confirmed in situ by the Proximity Ligation Assay (PLA). Further experiments demonstrated that c-Myc interacts with CUL4A and DDB1, components of the Cullin Ring E3 ubiquitin ligase 4 (CRL4) complex, in which PCNA functions as a cofactor. Mutations in the PIP box of c-Myc, as well as depletion of CUL4A by RNA interference, resulted in an increased stability of c-Myc protein. These results suggest that the interaction with PCNA functionally contributes to the regulation of c-Myc stability in early S phase via the CRL4 complex.