Human POLD3 coordinates leading and lagging strand in Mitotic DNA Synthesis
Turati, D.; Dionellis, V. S.; Tropia, L.; Halazonetis, T. D.
Show abstract
Deregulation of origin firing and licensing, shortage of deoxyribonucleotides in the cell and interference between transcription and replication are among the causes of DNA replication stress in cancer cells. This leads in various ways (notably, through common fragile sites expression and incomplete replication of late-replicating genomic regions during S phase) to the necessity of finishing DNA replication in mitosis by a mechanism called Mitotic DNA synthesis (MiDAS), which is related to Break-Induced Replication (BIR). Even if it is of primary importance for cancer cells, the molecular mechanism of MiDAS, and generally of BIR, is not yet well understood. Recently, the third subunit of the eukaryotic DNA polymerase delta (POLD3) has been recognized as a key player of BIR, though its role is not yet clear. In this work, using a protocol established in our group to map at high resolution newly replicated DNA at MiDAS sites, we provide new insights into the molecular role of POLD3 in this repair mechanism. In particular, by analyzing MiDAS in mutant HeLa clones lacking the PCNA-interacting domain of POLD3, we demonstrate that the interaction between POLD3 and PCNA is required for coordinating leading and lagging strand synthesis in MiDAS. This work represents an important step forward towards the comprehension of the molecular mechanisms of Mitotic DNA synthesis, the full understanding of which is of primary importance for the possible development of novel cancer therapies targeting BIR-related pathways.
Matching journals
The top 2 journals account for 50% of the predicted probability mass.
Similar papers in this journal
- Large-scale expansions and replication stalling of Friedreich's ataxia GAA repeats in an experimental mammalian system 96%
- The PIN1-p38-CtIP signaling axis protects stalled replication forks from deleterious degradation 96%
- SUMO protease and proteasome recruitment at the nuclear periphery differently affect replication dynamics at arrested forks. 95%
Similar papers in this journal
- Processing of a single ribonucleotide embedded into DNA by human nucleotide excision repair and DNA polymerase η 95%
- Sequential deregulation of histone marks, chromatin accessibility and gene expression in response to PROTAC-induced degradation of ASH2L 95%
- Human HMGN1 and HMGN2 are not required for transcription-coupled DNA repair 95%
Similar papers in this journal
"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.