نتایج جستجو برای: specific recombinase

تعداد نتایج: 1038905  

2013
Ilona Hauber Helga Hofmann-Sieber Jan Chemnitz Danilo Dubrau Janet Chusainow Rolf Stucka Philip Hartjen Axel Schambach Patrick Ziegler Karl Hackmann Evelin Schröck Udo Schumacher Christoph Lindner Adam Grundhoff Christopher Baum Markus G. Manz Frank Buchholz Joachim Hauber

Stable integration of HIV proviral DNA into host cell chromosomes, a hallmark and essential feature of the retroviral life cycle, establishes the infection permanently. Current antiretroviral combination drug therapy cannot cure HIV infection. However, expressing an engineered HIV-1 long terminal repeat (LTR) site-specific recombinase (Tre), shown to excise integrated proviral DNA in vitro, may...

Journal: :Molecular cell 2009
Hengyao Niu Lihong Wan Valeria Busygina YoungHo Kwon Jasmina A Allen Xue Li Ryan C Kunz Kazuishi Kubota Beatrice Wang Patrick Sung Kevan M Shokat Steven P Gygi Nancy M Hollingsworth

A preference for homologs over sister chromatids in homologous recombination is a fundamental difference in meiotic versus mitotic cells. In budding yeast, the bias for interhomolog recombination in meiosis requires the Dmc1 recombinase and the meiosis-specific kinase Mek1, which suppresses engagement of sister chromatids by the mitotic recombinase Rad51. Here, a combination of proteomic, bioch...

Journal: :Immunity 2002
Hong-Erh Liang Lih-Yun Hsu Dragana Cado Lindsay G Cowell Garnett Kelsoe Mark S Schlissel

Previous in vitro studies defined the minimal regions of RAG1 and RAG2 essential for V(D)J recombination. In order to characterize the role of the C-terminal "dispensable" portion of RAG2, we generated core-RAG2 knock-in mice. We found that the core-RAG2-containing recombinase complex is selectively defective in catalyzing V-to-DJ rearrangement at the IgH and TCRbeta loci, resulting in partial ...

2005
Angel-Luis García-Otín Florian Guillou

1. Abstract 2. Introduction 3. Site-specific recombinases 3.1. Cre and FLP recombinases 3.2. Recombinases in a mammalian environment 3.3. Further developments 3.4. Novel recombinases 4. Technology to manipulate the mouse genome 4.1. Gene transfer 4.2. Gene targeting 4.3. Nuclear transfer 5. Strategies for conditional gene targeting 5.1. Generation of floxed alleles 5.2. Promoter-specific driven...

Journal: :Nucleic acids research 2002
Elke Will Hannes Klump Nicole Heffner Maike Schwieger Bernhard Schiedlmeier Wolfram Ostertag Christopher Baum Carol Stocking

Site-specific recombination in genetically modified cells can be achieved by the activity of Cre recombinase from bacteriophage P1. Commonly an expression vector encoding Cre is introduced into cells; however, this can lead to undesired side-effects. Therefore, we tested whether cell-permeable Cre fusion proteins can be directly used for lox-specific recombination in a cell line tailored to shi...

2014
Thomas Gaj Shannon J. Sirk Ryan D. Tingle Andrew C. Mercer Mark C. Wallen Carlos F. Barbas

Despite recent advances in genome engineering made possible by the emergence of site-specific endonucleases, there remains a need for tools capable of specifically delivering genetic payloads into the human genome. Hybrid recombinases based on activated catalytic domains derived from the resolvase/invertase family of serine recombinases fused to Cys2-His2 zinc-finger or TAL effector DNA-binding...

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