Chromosomal translocations involving antigen receptor loci are common in lymphoid malignancies. Translocations require DNA double-strand breaks (DSBs) at two …
DNA double-strand break (DSB) repair pathway choice is governed by the opposing activities of 53BP1 and BRCA1. 53BP1 stimulates nonhomologous end joining (NHEJ) …
L Deriano, DB Roth - Annual review of genetics, 2013 - annualreviews.org
DNA double-strand breaks (DSBs) are common lesions that continually threaten genomic integrity. Failure to repair a DSB has deleterious consequences, including cell death …
The DNA damage response (DDR) is an organized network of multiple interwoven components evolved to repair damaged DNA and maintain genome fidelity. Conceptually …
C Boboila, FW Alt, B Schwer - Advances in immunology, 2012 - Elsevier
Classical nonhomologous end joining (C-NHEJ) is one of the two major known pathways for the repair of DNA double-strand breaks (DSBs) in mammalian cells. Our understanding of C …
P Frit, N Barboule, Y Yuan, D Gomez, P Calsou - DNA repair, 2014 - Elsevier
To cope with DNA double strand break (DSB) genotoxicity, cells have evolved two main repair pathways: homologous recombination which uses homologous DNA sequences as …
A Gupta, CR Hunt, S Chakraborty… - Radiation …, 2014 - meridian.allenpress.com
The p53-binding protein 1 (53BP1) is a well-known DNA damage response (DDR) factor, which is recruited to nuclear structures at the site of DNA damage and forms readily …
PJ Hung, B Johnson, BR Chen, AK Byrum… - Molecular cell, 2018 - cell.com
The modulator of retrovirus infection (MRI or CYREN) is a 30-kDa protein with a conserved N-terminal Ku-binding motif (KBM) and a C-terminal XLF-like motif (XLM). We show that MRI …
X Liu, Z Shao, W Jiang, BJ Lee, S Zha - Nature communications, 2017 - nature.com
Non-homologous end-joining (NHEJ) is the most prominent DNA double strand break (DSB) repair pathway in mammalian cells. PAXX is the newest NHEJ factor, which shares structural …