نتایج جستجو برای: nhej

تعداد نتایج: 1322  

Journal: :Current Biology 2001
Andreas Kegel Jimmy O.O. Sjöstrand Stefan U. Åström

Mutant yeast strains lacking the silencing proteins Sir2p, Sir3p, or Sir4p have a defect in a DNA double-strand break (DSB) repair pathway, called nonhomologous end joining (NHEJ). Mutations in sir genes also lead to the simultaneous expression of a and alpha mating type information, thus generating a nonmating haploid cell type with many properties shared with a/alpha diploids. We addressed wh...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2006
Pierre-Olivier Mari Bogdan I Florea Stephan P Persengiev Nicole S Verkaik Hennie T Brüggenwirth Mauro Modesti Giuseppina Giglia-Mari Karel Bezstarosti Jeroen A A Demmers Theo M Luider Adriaan B Houtsmuller Dik C van Gent

DNA double-strand break (DSB) repair by nonhomologous end joining (NHEJ) requires the assembly of several proteins on DNA ends. Although biochemical studies have elucidated several aspects of the NHEJ reaction mechanism, much less is known about NHEJ in living cells, mainly because of the inability to visualize NHEJ repair proteins at DNA damage. Here we provide evidence that a pulsed near IR l...

2012
Maria Jose Martin Raquel Juarez Luis Blanco

Non-homologous end-joining (NHEJ), the preferred pathway to repair double-strand breaks (DSBs) in higher eukaryotes, relies on a collection of molecular tools to process the broken ends, including specific DNA polymerases. Among them, Polµ is unique as it can catalyze DNA synthesis upon connection of two non-complementary ends. Here, we demonstrate that this capacity is intrinsic to Polµ, not c...

2012
Lisa A. Tobin Carine Robert Pratik Nagaria Saranya Chumsri William Twaddell Olga B. Ioffe George E. Greco Angela H. Brodie Alan E. Tomkinson Feyruz V. Rassool

Although hereditary breast cancers have defects in the DNA damage response that result in genomic instability, DNA repair abnormalities in sporadic breast cancers have not been extensively characterized. Recently, we showed that, relative to nontumorigenic breast epithelial MCF10A cells, estrogen receptor–positive (ERþ) MCF7 breast cancer cells and progesterone receptor–positive (PRþ) MCF7 brea...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2003
Y Dai B Kysela L A Hanakahi K Manolis E Riballo M Stumm T O Harville S C West M A Oettinger P A Jeggo

DNA nonhomologous end-joining (NHEJ) is the major pathway for repairing DNA double-strand breaks in mammalian cells. It also functions to carry out rearrangements at the specialized breaks introduced during V(D)J recombination. Here, we describe a patient with T(-)B(-) severe combined immunodeficiency, whose cells have defects closely resembling those of NHEJ-defective rodent cells. Cells deriv...

Journal: :Biochemical Society transactions 2009
Nigel C Brissett Aidan J Doherty

The NHEJ (non-homologous end-joining) pathway is one of the major mechanisms for repairing DSBs (double-strand breaks) that occur in genomic DNA. In common with eukaryotic organisms, many prokaryotes possess a conserved NHEJ apparatus that is essential for the repair of DSBs arising in the stationary phase of the cell cycle. Although the bacterial NHEJ complex is much more minimal than its euka...

Journal: :Journal of bacteriology 2007
Ralf Moeller Erko Stackebrandt Günther Reitz Thomas Berger Petra Rettberg Aidan J Doherty Gerda Horneck Wayne L Nicholson

The role of DNA repair by nonhomologous-end joining (NHEJ) in spore resistance to UV, ionizing radiation, and ultrahigh vacuum was studied in wild-type and DNA repair mutants (recA, splB, ykoU, ykoV, and ykoU ykoV mutants) of Bacillus subtilis. NHEJ-defective spores with mutations in ykoU, ykoV, and ykoU ykoV were significantly more sensitive to UV, ionizing radiation, and ultrahigh vacuum than...

2010
Sheetal Sharma Sathees C. Raghavan

Among various DNA damages, double-strand breaks (DSBs) are considered as most deleterious, as they may lead to chromosomal rearrangements and cancer when unrepaired. Nonhomologous DNA end joining (NHEJ) is one of the major DSB repair pathways in higher organisms. A large number of studies on NHEJ are based on in vitro systems using cell-free extracts. In this paper, we summarize the studies on ...

2005
Huichen Wang Bustanur Rosidi Ronel Perrault Minli Wang Lihua Zhang Frank Windhofer George Iliakis

Biochemical and genetic studies support the view that the majority of DNA double-strand breaks induced in the genome of higher eukaryotes by ionizing radiation are removed by two pathways of nonhomologous end joining (NHEJ) termed DNHEJ and B-NHEJ. Whereas D-NHEJ depends on the activities of the DNA-dependent protein kinase and DNA ligase IV/ XRCC4, components of B-NHEJ have not been identified...

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