» Articles » PMID: 32413071

DNA Replication Protein Cdc45 Directly Interacts with PCNA Via Its PIP Box in Leishmania Donovani and the Cdc45 PIP Box is Essential for Cell Survival

Overview
Journal PLoS Pathog
Specialty Microbiology
Date 2020 May 16
PMID 32413071
Citations 5
Authors
Affiliations
Soon will be listed here.
Abstract

DNA replication protein Cdc45 is an integral part of the eukaryotic replicative helicase whose other components are the Mcm2-7 core, and GINS. We identified a PIP box motif in Leishmania donovani Cdc45. This motif is typically linked to interaction with the eukaryotic clamp proliferating cell nuclear antigen (PCNA). The homotrimeric PCNA can potentially bind upto three different proteins simultaneously via a loop region present in each monomer. Multiple binding partners have been identified from among the replication machinery in other eukaryotes, and the concerted /sequential binding of these partners are central to the fidelity of the replication process. Though conserved in Cdc45 across Leishmania species and Trypanosoma cruzi, the PIP box is absent in Trypanosoma brucei Cdc45. Here we investigate the possibility of Cdc45-PCNA interaction and the role of such an interaction in the in vivo context. Having confirmed the importance of Cdc45 in Leishmania DNA replication we establish that Cdc45 and PCNA interact stably in whole cell extracts, also interacting with each other directly in vitro. The interaction is mediated via the Cdc45 PIP box. This PIP box is essential for Leishmania survival. The importance of the Cdc45 PIP box is also examined in Schizosaccharomyces pombe, and it is found to be essential for cell survival here as well. Our results implicate a role for the Leishmania Cdc45 PIP box in recruiting or stabilizing PCNA on chromatin. The Cdc45-PCNA interaction might help tether PCNA and associated replicative DNA polymerase to the DNA template, thus facilitating replication fork elongation. Though multiple replication proteins that associate with PCNA have been identified in other eukaryotes, this is the first report demonstrating a direct interaction between Cdc45 and PCNA, and while our analysis suggests the interaction may not occur in human cells, it indicates that it may not be confined to trypanosomatids.

Citing Articles

The SET29 and SET7 proteins of Leishmania donovani exercise non-redundant convergent as well as collaborative functions in moderating the parasite's response to oxidative stress.

Sharma V, Pal J, Dashora V, Chattopadhyay S, Kapoor Y, Singha B J Biol Chem. 2025; 301(3):108208.

PMID: 39842664 PMC: 11871502. DOI: 10.1016/j.jbc.2025.108208.


Functional Analysis and Experimental Validation of the Prognostic and Immune Effects of the Oncogenic Protein CDC45 in Breast Cancer.

Zhang J, Li L, Cao M, Liu X, Yi Z, Liu S Breast Cancer (Dove Med Press). 2025; 17():11-25.

PMID: 39811603 PMC: 11727330. DOI: 10.2147/BCTT.S497975.


IGF2BP2 promotes glycolysis and hepatocellular carcinoma stemness by stabilizing CDC45 mRNA via m6A modification.

Liao L, Wu T, Chen S, Yi Q, Xu M Cell Cycle. 2023; 22(20):2245-2263.

PMID: 37985379 PMC: 10730143. DOI: 10.1080/15384101.2023.2283328.


Correction: DNA replication protein Cdc45 directly interacts with PCNA via its PIP box in Leishmania donovani and the Cdc45 PIP box is essential for cell survival.

Yadav A, Sharma V, Pal J, Gulati P, Goel M, Chandra U PLoS Pathog. 2023; 19(3):e1011303.

PMID: 37000714 PMC: 10065266. DOI: 10.1371/journal.ppat.1011303.


KAP1 phosphorylation promotes the survival of neural stem cells after ischemia/reperfusion by maintaining the stability of PCNA.

Wang W, Yan T, Guo X, Cai H, Liang C, Huang L Stem Cell Res Ther. 2022; 13(1):290.

PMID: 35799276 PMC: 9264526. DOI: 10.1186/s13287-022-02962-5.


References
1.
Eickhoff P, Kose H, Martino F, Petojevic T, Abid Ali F, Locke J . Molecular Basis for ATP-Hydrolysis-Driven DNA Translocation by the CMG Helicase of the Eukaryotic Replisome. Cell Rep. 2019; 28(10):2673-2688.e8. PMC: 6737378. DOI: 10.1016/j.celrep.2019.07.104. View

2.
Yeeles J, Janska A, Early A, Diffley J . How the Eukaryotic Replisome Achieves Rapid and Efficient DNA Replication. Mol Cell. 2016; 65(1):105-116. PMC: 5222725. DOI: 10.1016/j.molcel.2016.11.017. View

3.
Choe K, Moldovan G . Forging Ahead through Darkness: PCNA, Still the Principal Conductor at the Replication Fork. Mol Cell. 2017; 65(3):380-392. PMC: 5302417. DOI: 10.1016/j.molcel.2016.12.020. View

4.
Szambowska A, Tessmer I, Prus P, Schlott B, Pospiech H, Grosse F . Cdc45-induced loading of human RPA onto single-stranded DNA. Nucleic Acids Res. 2017; 45(6):3217-3230. PMC: 5389570. DOI: 10.1093/nar/gkw1364. View

5.
Zhou J, Janska A, Goswami P, Renault L, Abid Ali F, Kotecha A . CMG-Pol epsilon dynamics suggests a mechanism for the establishment of leading-strand synthesis in the eukaryotic replisome. Proc Natl Acad Sci U S A. 2017; 114(16):4141-4146. PMC: 5402455. DOI: 10.1073/pnas.1700530114. View