Department of Microbiology, University of Delhi South Campus, New Delhi, India.
Department of Biophysics, University of Delhi South Campus, New Delhi, India.
PLoS Pathog. 2020 May 15;16(5):e1008190. doi: 10.1371/journal.ppat.1008190. eCollection 2020 May.
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.
DNA 复制蛋白 Cdc45 是真核复制解旋酶的组成部分,其其他成分是 Mcm2-7 核心和 GINS。我们在利什曼原虫 Cdc45 中鉴定出一个 PIP 盒基序。该基序通常与与真核夹增殖细胞核抗原 (PCNA) 的相互作用有关。三聚体 PCNA 可以通过每个单体中的环区潜在地同时结合多达三个不同的蛋白质。在其他真核生物的复制机制中已经鉴定出多个结合伙伴,这些伙伴的协同/顺序结合是复制过程保真度的核心。尽管在利什曼原虫物种和克氏锥虫中 Cdc45 是保守的,但 PIP 盒在布氏锥虫 Cdc45 中缺失。在这里,我们研究了 Cdc45-PCNA 相互作用的可能性以及这种相互作用在体内环境中的作用。在确认了 Cdc45 在利什曼原虫 DNA 复制中的重要性后,我们建立了 Cdc45 和 PCNA 在整个细胞提取物中稳定相互作用,并且在体外也直接相互作用。这种相互作用是通过 Cdc45 PIP 盒介导的。该 PIP 盒对利什曼原虫的生存至关重要。在酿酒酵母中也检查了 Cdc45 PIP 盒的重要性,发现它在这里对细胞生存也是必不可少的。我们的结果表明,Leishmania Cdc45 PIP 盒在招募或稳定染色质上的 PCNA 中起作用。Cdc45-PCNA 相互作用可能有助于将 PCNA 和相关的复制 DNA 聚合酶固定在 DNA 模板上,从而促进复制叉延伸。尽管在其他真核生物中已经鉴定出与 PCNA 相关的多种复制蛋白,但这是首次报道 Cdc45 和 PCNA 之间的直接相互作用,虽然我们的分析表明这种相互作用可能不会发生在人类细胞中,但它表明它可能不仅限于锥虫。