نتایج جستجو برای: dna repair enzymes

تعداد نتایج: 713751  

2014
Prabha Sarangi Veronika Altmannova Cory Holland Zdenka Bartosova Fanfan Hao Dorothea Anrather Gustav Ammerer Sang Eun Lee Lumir Krejci Xiaolan Zhao

DNA repair scaffolds mediate specific DNA and protein interactions in order to assist repair enzymes in recognizing and removing damaged sequences. Many scaffold proteins are dedicated to repairing a particular type of lesion. Here, we show that the budding yeast Saw1 scaffold is more versatile. It helps cells cope with base lesions and protein-DNA adducts through its known function of recruiti...

Journal: :The EMBO journal 1998
K G Berdal R F Johansen E Seeberg

Base excision repair is initiated by DNA glycosylases removing inappropriate bases from DNA. One group of these enzymes, comprising 3-methyladenine DNA glycosylase II (AlkA) from Escherichia coli and related enzymes from other organisms, has been found to have an unusual broad specificity towards quite different base structures. We tested whether such enzymes might also be capable of removing n...

2012
Amaya Azqueta Sergey Shaposhnikov Andrew R. Collins

The stability of the genome is of crucial importance, and yet the DNA molecule is prone to spontaneous loss of bases, and damage from exogenous and endogenous sources – with potentially mutagenic consequences. Damage can take the form of small alterations to bases (alkylation or oxidation); breaks in the sugar-phosphate backbone involving one or both strands (single or double strand breaks – SS...

Journal: :Molecules 2018
Oksana V Salomatina Irina I Popadyuk Alexandra L Zakharenko Olga D Zakharova Dmitriy S Fadeev Nina I Komarova Jóhannes Reynisson H John Arabshahi Raina Chand Konstantin P Volcho Nariman F Salakhutdinov Olga I Lavrik

An Important task in the treatment of oncological and neurodegenerative diseases is the search for new inhibitors of DNA repair system enzymes. Tyrosyl-DNA phosphodiesterase 1 (Tdp1) is one of the DNA repair system enzymes involved in the removal of DNA damages caused by topoisomerase I inhibitors. Thus, reducing the activity of Tdp1 can increase the effectiveness of currently used anticancer d...

2012
Mitch Leslie

RNF169 flips the repair switch P oulsen et al. describe an enzyme that helps a cell determine which repair method to use on DNA double-strand breaks (DSBs). Unrepaired DSBs can incite genomic chaos, spurring sections of chromosomes to relocate or even vanish. To ensure that doesn’t happen, a cell wraps a molecular bandage around a DSB. Enzymes arrive at the injury and ubiquitylate the surroundi...

Journal: :Genetics 2001
H M Kearney D T Kirkpatrick J L Gerton T D Petes

Meiotic recombination in Saccharomyces cerevisiae involves the formation of heteroduplexes, duplexes containing DNA strands derived from two different homologues. If the two strands of DNA differ by an insertion or deletion, the heteroduplex will contain an unpaired DNA loop. We found that unpaired loops as large as 5.6 kb can be accommodated within a heteroduplex. Repair of these loops involve...

2012
Yuliang Wu Robert M. Brosh

Conserved Iron-Sulfur (Fe-S) clusters are found in a growing family of metalloproteins that are implicated in prokaryotic and eukaryotic DNA replication and repair. Among these are DNA helicase and helicase-nuclease enzymes that preserve chromosomal stability and are genetically linked to diseases characterized by DNA repair defects and/or a poor response to replication stress. Insight to the s...

2007
Jason L. Parsons Bradley D. Preston Timothy R. O'Connor Grigory L. Dianov

Base excision repair (BER) is the major pathway for the repair of simple, non-bulky lesions in DNA that is initiated by a damage-specific DNA glycosylase. Several human DNA glycosylases exist that efficiently excise numerous types of lesions, although the close proximity of a single strand break (SSB) to a DNA adduct can have a profound effect on both BER and SSB repair. We recently reported th...

Journal: :Cellular & molecular biology letters 2004
Katarzyna Woźniak Janusz Błasiak

Nickel(II) is reported to be genotoxic, but the mechanisms underlying its genotoxicity are largely unknown. It can interfere with DNA repair and this may contribute to its genotoxicity. We studied the effect of nickel chloride on the repair of DNA damaged by UV radiation or N-methyl-N-nitro-N-nitrosoguanidine (MNNG) in human lymphocytes using the alkaline comet assay. Nickel(II) at 1 microM cau...

Journal: :Cancer research 2010
Lawrence A Loeb Susumu Nishimura

The 40th International Symposium of the Princess Takamatsu Cancer Research Fund, entitled "DNA Repair and Human Cancers," was held on November 10-12, 2009 at Hotel Grand Palace, Tokyo, Japan. The meeting focused on the role of DNA repair in preventing mutations by endogenous and exogenous DNA damage and increasing the efficacy of chemotherapeutic agents by interfering with DNA repair. The 14 pr...

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