Literature DB >> 10852701

Transcriptional properties of genomic transgene integration sites marked by electroporation or retroviral infection.

A Baer1, D Schübeler, J Bode.   

Abstract

As a possible consequence of their survival strategy, proviruses are predominantly found in transcription-promoting genomic sites. For certain applications, these findings have led to the preferential use of retroviral vectors for the stable integration of transgenes. This study demonstrates that transcription levels of single-copy proviruses, which have been established either by infection or by single-copy transfection (electroporation), are rather comparable. Therefore, electroporation is suggested as an alternative gene transfer route in cases where the use of infectious retroviral vehicles is to be avoided due to safety considerations. A difference between clones derived from these two gene transfer routes concerns the inactivation pattern which, for electroporated clones, is an exclusive property of the low expressers. This difference may be due to the nature of the illegitimate recombination event which is thought to be less invasive if catalyzed by the retroviral integrase. Substantial differences between infection and Ca phosphate-mediated transfection that have been reported earlier are explained by the respective transfection parameters.

Entities:  

Mesh:

Year:  2000        PMID: 10852701     DOI: 10.1021/bi992957o

Source DB:  PubMed          Journal:  Biochemistry        ISSN: 0006-2960            Impact factor:   3.162


  8 in total

1.  Methylation-mediated proviral silencing is associated with MeCP2 recruitment and localized histone H3 deacetylation.

Authors:  M C Lorincz; D Schübeler; M Groudine
Journal:  Mol Cell Biol       Date:  2001-12       Impact factor: 4.272

2.  Chromatin insulation by a transcriptional activator.

Authors:  Nathan B Sutter; David Scalzo; Steven Fiering; Mark Groudine; David I K Martin
Journal:  Proc Natl Acad Sci U S A       Date:  2003-01-23       Impact factor: 11.205

3.  Performance of genomic bordering elements at predefined genomic loci.

Authors:  Sandra Goetze; Alexandra Baer; Silke Winkelmann; Kristina Nehlsen; Jost Seibler; Karin Maass; Jürgen Bode
Journal:  Mol Cell Biol       Date:  2005-03       Impact factor: 4.272

4.  Recommended Method for Chromosome Exploitation: RMCE-based Cassette-exchange Systems in Animal Cell Biotechnology.

Authors:  André Oumard; Junhua Qiao; Thomas Jostock; Jiandong Li; Juergen Bode
Journal:  Cytotechnology       Date:  2006-06-14       Impact factor: 2.058

5.  Mouse embryonic stem cells, but not somatic cells, predominantly use homologous recombination to repair double-strand DNA breaks.

Authors:  Elisia D Tichy; Resmi Pillai; Li Deng; Li Liang; Jay Tischfield; Sandy J Schwemberger; George F Babcock; Peter J Stambrook
Journal:  Stem Cells Dev       Date:  2010-08-05       Impact factor: 3.272

6.  Enhanceosome formation over the beta interferon promoter underlies a remote-control mechanism mediated by YY1 and YY2.

Authors:  Martin Klar; Juergen Bode
Journal:  Mol Cell Biol       Date:  2005-11       Impact factor: 4.272

7.  DNA fragments binding CTCF in vitro and in vivo are capable of blocking enhancer activity.

Authors:  Dmitry A Didych; Elena S Kotova; Segey B Akopov; Lev G Nikolaev; Eugene D Sverdlov
Journal:  BMC Res Notes       Date:  2012-04-05

8.  Recombinant protein expression by targeting pre-selected chromosomal loci.

Authors:  Kristina Nehlsen; Roland Schucht; Leonor da Gama-Norton; Wolfgang Krömer; Alexandra Baer; Aziz Cayli; Hansjörg Hauser; Dagmar Wirth
Journal:  BMC Biotechnol       Date:  2009-12-14       Impact factor: 2.563

  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.