نتایج جستجو برای: recq

تعداد نتایج: 711  

Journal: :Cancer research 2006
Ze-Hong Miao V Ashutosh Rao Keli Agama Smitha Antony Kurt W Kohn Yves Pommier

RecQ helicase BLM-deficient cells are characteristically hypersensitive to 4-nitroquinoline-1-oxide (4NQO). We recently reported that isogenic BLM-deficient cells (PNSG13) are more sensitive than BLM-complemented cells (PNSF5) to camptothecin, which specifically traps topoisomerase I cleavage complexes (Top1cc). We now report that PNSG13 are also 3.5-fold more sensitive to 4NQO compared with PN...

Journal: :The EMBO journal 2009
Kara A Bernstein Erika Shor Ivana Sunjevaric Marco Fumasoni Rebecca C Burgess Marco Foiani Dana Branzei Rodney Rothstein

Mutations in human homologues of the bacterial RecQ helicase cause diseases leading to cancer predisposition and/or shortened lifespan (Werner, Bloom, and Rothmund-Thomson syndromes). The budding yeast Saccharomyces cerevisiae has one RecQ helicase, Sgs1, which functions with Top3 and Rmi1 in DNA repair. Here, we report separation-of-function alleles of SGS1 that suppress the slow growth of top...

2009
Monika Aggarwal Robert M. Brosh

Werner syndrome (WS) is a premature aging disorder characterized by genomic instability. The WRN gene defective in WS encodes a protein with both helicase and exonuclease activities that interacts with proteins implicated in DNA metabolism. To understand its genetic functions, we examined the ability of human WRN to rescue phenotypes associated with sgs1, the sole RecQ helicase in Saccharomyces...

Journal: :Genetics 1998
P Sánchez-Alonso P Guzmán

In this study we have established the structure of chromosome ends in the basidiomycete fungus Ustilago maydis. We isolated and characterized several clones containing telomeric regions and found that as in other organisms, they consist of middle repeated DNA sequences. Two principal types of sequence were found: UTASa was highly conserved in nucleotide sequence and located almost exclusively a...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2006
Charmain T Courcelle Kin-Hoe Chow Andrew Casey Justin Courcelle

DNA lesions that arrest replication can lead to rearrangements, mutations, or lethality when not processed accurately. After UV-induced DNA damage in Escherichia coli, RecA and several recF pathway proteins are thought to process arrested replication forks and ensure that replication resumes accurately. Here, we show that the RecJ nuclease and RecQ helicase, which partially degrade the nascent ...

2017
Stephen R. Okoniewski Lyle Uyetake Thomas T. Perkins

Single-molecule force spectroscopy provides insight into how proteins bind to and move along DNA. Such studies often embed a single-stranded (ss) DNA region within a longer double-stranded (ds) DNA molecule. Yet, producing these substrates remains laborious and inefficient, particularly when using the traditional three-way hybridization. Here, we developed a force-activated substrate that yield...

2016
Jun Xia Li-Tzu Chen Qian Mei Chien-Hui Ma Jennifer A Halliday Hsin-Yu Lin David Magnan John P Pribis Devon M Fitzgerald Holly M Hamilton Megan Richters Ralf B Nehring Xi Shen Lei Li David Bates P J Hastings Christophe Herman Makkuni Jayaram Susan M Rosenberg

DNA repair by homologous recombination (HR) underpins cell survival and fuels genome instability, cancer, and evolution. However, the main kinds and sources of DNA damage repaired by HR in somatic cells and the roles of important HR proteins remain elusive. We present engineered proteins that trap, map, and quantify Holliday junctions (HJs), a central DNA intermediate in HR, based on catalytica...

2012
Takashi Tadokoro Tomasz Kulikowicz Lale Dawut Deborah L. Croteau Vilhelm A. Bohr

Werner protein (WRN), member of the RecQ helicase family, is a helicase and exonuclease, and participates in multiple DNA metabolic processes including DNA replication, recombination and DNA repair. Mutations in the WRN gene cause Werner syndrome, associated with premature aging, genome instability and cancer predisposition. The RecQ C-terminal (RQC) domain of WRN, containing α2-α3 loop and β-w...

Journal: :Nucleic Acids Research 2005
Baomin Li Nathan Conway Sonia Navarro Luca Comai Lucio Comai

Werner syndrome is associated with mutations in the DNA helicase RecQ3 [a.k.a. Homo sapiens (hs)WRN]. The function of hsWRN is unknown although biochemical studies suggest a role in DNA ends stability and repair. Unlike other RecQ family members, hsWRN possesses an N-terminal domain with exonuclease activity, which is stimulated by interaction with the Ku heterodimer. While this interaction is ...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید