Open AccessMedicineBiology

T. Popławski, J. Błasiak

2005Postepy Biochemii

DOI: 10.18388/abp.2003_3622

tlooto Summary

This review focuses on the mechanisms and main components of the NHEJ system in eukaryotes, which include the catalytic subunit of DNA protein kinase, Ku proteins, XRCC4, DNA ligase IV, and Artemis.

Abstract

DNA double strand breaks (DSB) are the most serious form of DNA damage. Repair of DSBs is important to prevent chromosomal fragmentation, translocations and deletions. Non-homologous end joining (NHEJ) is one of three major pathways for the repair of DSBs in human cells. In this process two DNA ends are joined directly, usually with no sequence homology, although in the case of same polarity of the single stranded overhangs in DSBs, regions of microhomology are utilized. NHEJ is typically imprecise, a characteristic that is useful for immune diversification in lymphocytes in V(D)J recombination. The main components of the NHEJ system in eukaryotes are the catalytic subunit of DNA protein kinase (DNA-PKcs), Ku proteins, XRCC4, DNA ligase IV, and Artemis. This review focuses on the mechanisms an dregulation of DSB repair by NHEJ in mammalian cells.

Citation format

POPŁAWSKI, T.; BŁASIAK, J. [Non-homologous DNA end joining]. Postepy Biochemii, 2005, 51 3: 328–38.