نتایج جستجو برای: ژن xrcc4

تعداد نتایج: 16150  

Journal: :Journal of immunology 2002
Kyung-Jong Lee Xingwen Dong Jingsong Wang Yoshihiko Takeda William S Dynan

The nonhomologous end-joining pathway is the principal mechanism for repair of ionizing radiation-induced, double-strand breaks in mammalian cells. Three polypeptides in this pathway, including the two subunits of Ku protein and the catalytic subunit of the DNA-dependent protein kinase, are known targets of autoantibodies in systemic rheumatic diseases. Here we show that two additional polypept...

Journal: :Journal of immunology 2011
Jennifer Eccleston Catherine Yan Karen Yuan Frederick W Alt Erik Selsing

In the absence of core nonhomologous end-joining (NHEJ) factors, Ab gene class-switch recombination (CSR) uses an alternative end-joining (A-EJ) pathway to recombine switch (S) region DNA breaks. Previous reports showing decreased S-junction microhomologies in MSH2-deficient mice and an exonuclease 1 (EXO1) role in yeast microhomology-mediated end joining suggest that mismatch repair (MMR) prot...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2000
Y Gu J Sekiguchi Y Gao P Dikkes K Frank D Ferguson P Hasty J Chun F W Alt

Mammalian nonhomologous DNA end joining employs Ku70, Ku80, DNA-dependent protein kinase catalytic subunit (DNA-PKcs), XRCC4, and DNA ligase IV (Lig4). Herein, we show that Ku70 and Ku80 deficiency but not DNA-PKcs deficiency results in dramatically increased death of developing embryonic neurons in mice. The Ku-deficient phenotype is qualitatively similar to, but less severe than, that associa...

2010
Cristian Boboila Catherine Yan Duane R. Wesemann Mila Jankovic Jing H. Wang John Manis Andre Nussenzweig Michel Nussenzweig Frederick W. Alt

The classical nonhomologous end-joining (C-NHEJ) DNA double-strand break (DSB) repair pathway employs the Ku70/80 complex (Ku) for DSB recognition and the XRCC4/DNA ligase 4 (Lig4) complex for ligation. During IgH class switch recombination (CSR) in B lymphocytes, switch (S) region DSBs are joined by C-NHEJ to form junctions either with short microhomologies (MHs; "MH-mediated" joins) or no hom...

2016
Howard H. Y. Chang Go Watanabe Christina A. Gerodimos Takashi Ochi Tom L. Blundell Stephen P. Jackson Michael R. Lieber

The nonhomologous DNA end-joining (NHEJ) pathway is a key mechanism for repairing dsDNA breaks that occur often in eukaryotic cells. In the simplest model, these breaks are first recognized by Ku, which then interacts with other NHEJ proteins to improve their affinity at DNA ends. These include DNA-PKcs and Artemis for trimming the DNA ends; DNA polymerase μ and λ to add nucleotides; and the DN...

2014
Masahiro Terasawa Akira Shinohara Miki Shinohara

DNA double-strand breaks (DSBs) can be repaired by one of two major pathways-non-homologous end-joining (NHEJ) and homologous recombination (HR)-depending on whether cells are in G1 or S/G2 phase, respectively. However, the mechanisms of DSB repair during M phase remain largely unclear. In this study, we demonstrate that transient treatment of M-phase cells with the chemotherapeutic topoisomera...

Journal: :American journal of human genetics 2015
Jennie E Murray Mirjam van der Burg Hanna IJspeert Paula Carroll Qian Wu Takashi Ochi Andrea Leitch Edward S Miller Boris Kysela Alireza Jawad Armand Bottani Francesco Brancati Marco Cappa Valerie Cormier-Daire Charu Deshpande Eissa A Faqeih Gail E Graham Emmanuelle Ranza Tom L Blundell Andrew P Jackson Grant S Stewart Louise S Bicknell

Non-homologous end joining (NHEJ) is a key cellular process ensuring genome integrity. Mutations in several components of the NHEJ pathway have been identified, often associated with severe combined immunodeficiency (SCID), consistent with the requirement for NHEJ during V(D)J recombination to ensure diversity of the adaptive immune system. In contrast, we have recently found that biallelic mut...

Journal: :The Journal of Experimental Medicine 2008
Jing H. Wang Frederick W. Alt Monica Gostissa Abhishek Datta Michael Murphy Marat B. Alimzhanov Kristen M. Coakley Klaus Rajewsky John P. Manis Catherine T. Yan

Nonhomologous end-joining (NHEJ) repairs DNA double-strand breaks (DSBs) during V(D)J recombination in developing lymphocytes and during immunoglobulin (Ig) heavy chain (IgH) class switch recombination (CSR) in peripheral B lymphocytes. We now show that CD21-cre-mediated deletion of the Xrcc4 NHEJ gene in p53-deficient peripheral B cells leads to recurrent surface Ig-negative B lymphomas ("CXP ...

Journal: :journal of biomedical physics and engineering 0
m valizadeh tehran university of medical sciences a shirazi tehran university of medical sciencesسازمان اصلی تایید شده: دانشگاه علوم پزشکی تهران (tehran university of medical sciences) p izadi tehran university of medical sciencesسازمان اصلی تایید شده: دانشگاه علوم پزشکی تهران (tehran university of medical sciences) j tavakkoly bazzaz tehran university of medical sciencesسازمان اصلی تایید شده: دانشگاه علوم پزشکی تهران (tehran university of medical sciences) h rezaeejam tehran university of medical sciencesسازمان اصلی تایید شده: دانشگاه علوم پزشکی تهران (tehran university of medical sciences)

background: after radiation therapy (rt), some health hazards including dna damages may occur where melatonin can play a protective role due to free radical generation. on the other hand, serious accidental overexposures may occur during rt due to nuclear accidents which necessitate the need for study on exposure to high-dose radiations during treatments. objective: the aim of this study was to...

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه شیراز - دانشکده علوم پایه 1393

آسیب های وارده به dna می تواند نواقصی را در رونوشت rna و پروتئین های ترجمه شده ی آنها بر جای گذارد که باید ترمیم گردد. یکی از این آسیب ها شکست های دو رشته ای dna است که سیستم ترمیمی این نوع شکست، شامل دو مسیرnonhomologous end joining (nhej) و homologous recombination (hr) می باشد. هر گونه تغییرات مثل چند شکلی های ژنتیکی در این دو مسیر ترمیمی می تواند منجر به سرطان شود. پروتئین های درگیر در مسیر...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید