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Generation and characterization of tTS‐H4: a novel transcriptional repressor that is compatible with the reverse tetracycline‐controlled TET‐ON system
Author(s) -
Bockamp Ernesto,
Christel Cerstin,
Hameyer Dorothe,
Khobta Andriy,
Maringer Marko,
Reis Marco,
Heck Rosario,
CabezasWallscheid Nina,
Epe Bernd,
OeschBartlomowicz Barbara,
Kaina Bernd,
Schmitt Steffen,
Eshkind Leonid
Publication year - 2007
Publication title -
the journal of gene medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.689
H-Index - 91
eISSN - 1521-2254
pISSN - 1099-498X
DOI - 10.1002/jgm.1012
Subject(s) - tetr , repressor , biology , effector , gene silencing , yy1 , regulation of gene expression , microbiology and biotechnology , promoter , transcription (linguistics) , transcriptional regulation , gene , gene expression , genetics , linguistics , philosophy
Background Conditional gene regulatory systems ensuring tight and adjustable expression of therapeutic genes are central for developing future gene therapy strategies. Among various regulatory systems, tetracycline‐controlled gene expression has emerged as a safe and reliable option. Moreover, the tightness of tetracycline‐regulated gene switches can be substantially improved by complementing transcriptional activators with antagonizing repressors. Methods To develop novel tetracycline‐responsive transcriptional repressors, we fused various transcriptional silencing domains to the TetR (B/E) DNA‐binding and dimerization domain of the Tn10 ‐encoded tetracycline resistance operon (TetR (B/E)). The resulting fusion proteins were individually tested for their ability to repress transcription of the constitutively active hypoxanthine phosphoribosyltransferase (HPRT) promoter. In addition, compatibility with the commonly used reverse tetracycline‐controlled transactivator system (rtTA‐system) and responsiveness to the pharmacological effector doxycycline (DOX) were evaluated. Finally, inducibility, effector‐dependent promoter activity and the modification of histone H3 and H4 of the active versus the repressed target promoter were determined. Results Fusion of the human deacetylase 4 (HDAC4) carboxy‐terminal silencing domain to TetR (B/E) resulted in a functional transcriptional repressor. This novel repressor, termed tTS‐H4, efficiently reduced the activity of the murine HPRT promoter and a constitutively active human cytomegalovirus (hCMV) minimal promoter. Furthermore, combining tTS‐H4 with the rtTA transcriptional activator allowed for grading, turning off and resuming target gene expression over several orders of magnitude without background. Conclusions The tTS‐H4 repressor is compatible with the commonly used rtTA transcriptional activation system and is a versatile new tool for tightly and adjustably regulating conditional gene expression. Copyright © 2007 John Wiley & Sons, Ltd.