Impact of PARP1, PARP2 & PARP3 on the Base Excision Repair of Nucleosomal DNA

M. M. Kutuzov, E. A. Belousova, E. S. Ilina, O. I. Lavrik

Результат исследования: Публикации в книгах, отчётах, сборниках, трудах конференцийглава/разделнаучнаярецензирование

1 Цитирования (Scopus)


DNA is constantly attacked by different damaging agents; therefore, it requires frequent repair. On the one hand, the base excision repair (BER) system is responsible for the repair of the most frequent DNA lesions. On the other hand, the formation of poly(ADP-ribose) is one of the main DNA damage response reactions that is catalysed by members of the PARP family. PARP1, which belongs to the PARP family and performs approximately 90% of PAR synthesis in cells, could be considered a main regulator of the BER process. Most of the experimental data concerning BER investigation have been obtained using naked DNA. However, in the context of the eukaryotic cell, DNA is compacted in the nucleus, and the lowest compaction level is represented by the nucleosome. Thus, the organization of DNA into the nucleosome impacts the DNA-protein interactions that are involved in BER processes. Poly(ADP-ribosyl)ation (PARylation) is thought to regulate the initiation of the BER process at the chromatin level. In this review, we focus on the mechanisms involved in BER in the nucleosomal context and the potential effect of PARylation, which is catalysed by DNA-dependent PARP1, PARP2 and PARP3 proteins, on this process.

Язык оригиналаанглийский
Название основной публикацииMechanisms of Genome Protection and Repair
РедакторыDmitry O. Zharkov
ИздательSpringer, Cham
Число страниц11
ISBN (электронное издание)978-3-030-41283-8
ISBN (печатное издание)978-3-030-41282-1, 978-3-030-41285-2
СостояниеОпубликовано - 8 мая 2020

Серия публикаций

НазваниеAdvances in experimental medicine and biology
ISSN (печатное издание)0065-2598

Предметные области OECD FOS+WOS



Подробные сведения о темах исследования «Impact of PARP1, PARP2 & PARP3 on the Base Excision Repair of Nucleosomal DNA». Вместе они формируют уникальный семантический отпечаток (fingerprint).