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Structural and functional basis for ADP-ribose and poly(ADP-ribose) binding by viral macro domains.

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  • Macro Domains Constitute A Protein Module Family Found Associated With Specific Histones And Protein
  • In Addition
  • A Small Number Of Animal Rna Viruses
  • Such As Corona- And Toroviruses
  • Alphaviruses
  • And Hepatitis E Virus
  • Encode Macro Domains For Which
  • However
  • Structural And Functional Information Is Extremely Limited
  • Here
  • We Characterized The Macro Domains From Hepatitis E Virus
  • Semliki Forest Virus
  • And Severe Acute Respiratory Syndrome Coronavirus (Sars-Cov)
  • The Crystal Structure Of The Sars-Cov Macro Domain Was Determined At 1
  • 8-Å Resolution In Complex With Adp-Ribose
  • Information Derived From Structural
  • Mutational
  • And Sequence Analyses Suggests A Close Phylogenetic And
  • Most Probably
  • Functional Relationship Between Viral And Cellular Macro Domain Homologs
  • The Data Revealed That Viral Macro Domains Have Relatively Poor Adp-Ribose 1"-Phosphohydrolase Activ
  • Collectively
  • These Results Suggest To Further Evaluate The Role Of Viral Macro Domains In Host Response To Viral
  • Biology
  • Design
  • Engineering


31 From: Methods in Molecular Biology, vol. 435: Chromosomal Mutagenesis Edited by: G. Davis and K. J. Kayser © Humana Press Inc., Totowa, NJ 3 Robust Cell Line Development Using Meganucleases Jean-Pierre Cabaniols and Frédéric Pâques Summary Cell line development for protein production or for the screening of drug targets requires the reproducible and stable expression of transgenes. Such cell lines can be engineered with meganu- cleases, sequence-specific endonucleases that recognize large DNA target sites. These proteins are powerful tools for genome engineering because they can increase homologous gene targeting by several orders of magnitude in the vicinity of their cleavage site. Here, we describe in details the use of meganucleases for gene targeting in Chinese hamster ovary-K1 cells, with a special emphasis on a gene insertion procedure using a promoter-less marker gene for selection. We have also monitored the expression of genes inserted by meganucleases-induced recombination, and show that expres- sion is reproducible among different targeted clones, and stable over a 4 mo period. These experi- ments were conducted with the natural yeast I-SceI meganuclease, but the general design and process can also be applied to engineered meganucleases. Key Words: Cell line development; double-strand break; gene targeting; homologous recombi- nation; I-SceI; meganucleases; protein production. 1. Introduction Homologous recombination is a powerful tool for genome engineering. Since the first gene targeting experiments in yeast more than 25 yr ago (1,2), homologous recombination (HR) has been used to insert, replace, or delete genomic sequences in a variety of cells (3–5). However, targeted events occur at a very low frequency in mammalian cells. The frequency of HR can be significantly increased by a specific DNA double-strand break (DSB) in the targeted locus (6,7). Such DSBs can be delivered with meganucleases, sequence-specific endonucleases that recog- nize large DNA target si

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