DNA-protein crosslink proteases in genome stability.
Annamaria RuggianoKristijan RamadanPublished in: Communications biology (2021)
Proteins covalently attached to DNA, also known as DNA-protein crosslinks (DPCs), are common and bulky DNA lesions that interfere with DNA replication, repair, transcription and recombination. Research in the past several years indicates that cells possess dedicated enzymes, known as DPC proteases, which digest the protein component of a DPC. Interestingly, DPC proteases also play a role in proteolysis beside DPC repair, such as in degrading excess histones during DNA replication or controlling DNA replication checkpoints. Here, we discuss the importance of DPC proteases in DNA replication, genome stability and their direct link to human diseases and cancer therapy.
Keyphrases
- circulating tumor
- cell free
- single molecule
- cancer therapy
- protein protein
- endothelial cells
- induced apoptosis
- nucleic acid
- dna damage
- amino acid
- binding protein
- genome wide
- drug delivery
- circulating tumor cells
- oxidative stress
- signaling pathway
- dna repair
- cell death
- transcription factor
- cell proliferation
- induced pluripotent stem cells