نتایج جستجو برای: homologous recombination repair system

تعداد نتایج: 2445402  

Journal: :Microbiology and molecular biology reviews : MMBR 1999
F Pâques J E Haber

The budding yeast Saccharomyces cerevisiae has been the principal organism used in experiments to examine genetic recombination in eukaryotes. Studies over the past decade have shown that meiotic recombination and probably most mitotic recombination arise from the repair of double-strand breaks (DSBs). There are multiple pathways by which such DSBs can be repaired, including several homologous ...

2014
Kathryn P. Pennington Tom Walsh Maria I. Harrell Ming K. Lee Christopher C. Pennil Mara H. Rendi Anne Thornton Barbara M. Norquist Silvia Casadei Alexander S. Nord Kathy J. Agnew Colin C. Pritchard Sheena Scroggins Rochelle L. Garcia Mary-Claire King Elizabeth M. Swisher

Purpose: Hallmarks of germline BRCA1/2-associated ovarian carcinomas include chemosensitivity and improved survival. The therapeutic impact of somatic BRCA1/2 mutations and mutations in other homologous recombination DNA repair genes is uncertain. Experimental Design: Using targeted capture and massively parallel genomic sequencing, we assessed 390ovarian carcinomas for germline and somatic los...

Journal: :Biological chemistry Hoppe-Seyler 1996
M Hagmann K Adlkofer P Pfeiffer R Bruggmann O Georgiev D Rungger W Schaffner

We have developed a versatile plasmid vector (pReco-sigma) for recombination studies. When linearized and introduced into the cells of interest, pReco-sigma allows the simultaneous determination of the relative frequencies of homologous recombination versus nonhomologous DNA-end joining (also termed end-to-end joining), the latter an example of illegitimate recombination processes. As a system ...

Journal: :PLoS Genetics 2006
Richard Bowater Aidan J Doherty

DNA double-strand breaks (DSBs) are one of the most dangerous forms of DNA lesion that can result in genomic instability and cell death. Therefore cells have developed elaborate DSB-repair pathways to maintain the integrity of genomic DNA. There are two major pathways for the repair of DSBs in eukaryotes: homologous recombination and non-homologous end-joining (NHEJ). Until very recently, the N...

Journal: :Frontiers in bioscience 2017
Alexis Stein Elaine A Sia

The accurate maintenance of mitochondrial DNA (mtDNA) is required in order for eukaryotic cells to assemble a functional electron transport chain. This independently-maintained genome relies on nuclear-encoded proteins that are imported into the mitochondria to carry out replication and repair processes. Decades of research has made clear that mitochondria employ robust and varied mtDNA repair ...

2011
Jeffrey Parvin Natsuko Chiba Derek Ransburgh

The functional analysis of missense mutations can be complicated by the presence in the cell of the endogenous protein. Structure-function analyses of the BRCA1 have been complicated by the lack of a robust assay for the full length BRCA1 protein and the difficulties inherent in working with cell lines that express hypomorphic BRCA1 protein. We developed a system whereby the endogenous BRCA1 pr...

2013
Leonardo Bee Sonia Fabris Roberto Cherubini Maddalena Mognato Lucia Celotti

This study investigated the efficiency of Non-Homologous End Joining (NHEJ) and Homologous Recombination (HR) repair systems in rejoining DNA double-strand breaks (DSB) induced in CCD-34Lu cells by different γ-ray doses. The kinetics of DNA repair was assessed by analyzing the fluorescence decrease of γ-H2AX foci measured by SOID (Sum Of Integrated Density) parameter and counting foci number in...

Journal: :Mutation research 2003
Thomas Helleday

Homologous recombination (HR) is essential for cellular survival in mammals. In this review, the substrates for HR, the pathways of repair, and their end products (i.e. sister chromatid exchange (SCE), gene conversion, deletions or tandem duplications) are discussed. HR is involved in the repair of DNA double-strand breaks (DSBs) and DNA lesions that occur at replication forks. A classical DSB ...

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