Literature DB >> 9478886

A regulatory system for target gene expression.

M M Burcin1, B W O'Malley, S Y Tsai.   

Abstract

Temporally-regulated expression of endogenous genes is a desirable goal in stable cell line and transgenic animal systems, as well as in clinical gene therapy. Protocols for introducing genes into stable cell lines and experimental animals are often unsatisfactory due to the constitutive expression of such transgenes. To circumvent this problem we have demonstrated specific and temporally regulable expression of a target gene in vivo effected by a chimeric regulator in response to an orally-administered, non-toxic chemical. This regulatory system utilizes a chimeric regulator GLVP, consisting of a mutated human progesterone receptor ligand binding domain (PRLBD-delta) fused to the yeast GAL4 DNA binding domain (DBD) and the HSV VP16 transcriptional activation domain and whose activity is solely regulable by non-physiological doses of RU486 but not by progesterone or other endogenous progestins. Replacing the activation domain of the chimeric regulator with a transcriptional repression domain results in inducible repression of target gene expression in vitro. Our regulatory system functions in transient and stable transfections as well as in transgenic animals, and will have a wide variety of potential applications.

Entities:  

Mesh:

Substances:

Year:  1998        PMID: 9478886     DOI: 10.2741/a258

Source DB:  PubMed          Journal:  Front Biosci        ISSN: 1093-4715


  15 in total

Review 1.  Advanced transgenic and gene-targeting approaches.

Authors:  X Gao; A Kemper; B Popko
Journal:  Neurochem Res       Date:  1999-09       Impact factor: 3.996

2.  A conditional tissue-specific transgene expression system using inducible GAL4.

Authors:  T Osterwalder; K S Yoon; B H White; H Keshishian
Journal:  Proc Natl Acad Sci U S A       Date:  2001-10-23       Impact factor: 11.205

Review 3.  Transgenic models of pancreatic cancer.

Authors:  Andrew M Lowy
Journal:  Int J Gastrointest Cancer       Date:  2003

Review 4.  Regulatable gene expression systems for gene therapy applications: progress and future challenges.

Authors:  S Goverdhana; M Puntel; W Xiong; J M Zirger; C Barcia; J F Curtin; E B Soffer; S Mondkar; G D King; J Hu; S A Sciascia; M Candolfi; D S Greengold; P R Lowenstein; M G Castro
Journal:  Mol Ther       Date:  2005-08       Impact factor: 11.454

Review 5.  Regulatable gene expression systems for gene therapy.

Authors:  Nuria Vilaboa; Richard Voellmy
Journal:  Curr Gene Ther       Date:  2006-08       Impact factor: 4.391

Review 6.  A next step in adeno-associated virus-mediated gene therapy for neurological diseases: regulation and targeting.

Authors:  Abdelwahed Chtarto; Olivier Bockstael; Terence Tshibangu; Olivier Dewitte; Marc Levivier; Liliane Tenenbaum
Journal:  Br J Clin Pharmacol       Date:  2013-08       Impact factor: 4.335

7.  Seizure suppression by gain-of-function escargot mutations.

Authors:  Daria S Hekmat-Scafe; Kim N Dang; Mark A Tanouye
Journal:  Genetics       Date:  2005-01-16       Impact factor: 4.562

8.  Suppression of colorectal tumor growth by regulated survivin targeting.

Authors:  Binghua Li; Junkai Fan; Xinran Liu; Rong Qi; Linan Bo; Jinfa Gu; Cheng Qian; Xinyuan Liu
Journal:  J Mol Med (Berl)       Date:  2006-11-01       Impact factor: 4.599

9.  Spatial and temporal control of gene expression in Drosophila using the inducible GeneSwitch GAL4 system. I. Screen for larval nervous system drivers.

Authors:  Louise Nicholson; Gunisha K Singh; Thomas Osterwalder; Gregg W Roman; Ronald L Davis; Haig Keshishian
Journal:  Genetics       Date:  2008-01       Impact factor: 4.562

10.  A novel estrogen receptor intramolecular folding-based titratable transgene expression system.

Authors:  Ramasamy Paulmurugan; Parasuraman Padmanabhan; Byeong-Cheol Ahn; Sunetra Ray; Juergen K Willmann; Tarik F Massoud; Sandip Biswal; Sanjiv S Gambhir
Journal:  Mol Ther       Date:  2009-08-04       Impact factor: 11.454

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.