DNA-binding of the Tet-transactivator curtails antigen-induced lymphocyte activation in mice.

ABSTRACT: The Tet-On/Off system for conditional transgene expression constitutes state-of-the-art technology to study gene function by facilitating inducible expression in a timed and reversible manner. Several studies documented the suitability and versatility of this system to trace lymphocyte fate and to conditionally express oncogenes or silence tumour suppressor genes in vivo. Here, we show that expression of the tetracycline/doxycycline-controlled Tet-transactivator, while tolerated well during development and in immunologically unchallenged animals, impairs the expansion of antigen-stimulated T and B cells and thereby curtails adaptive immune responses in vivo. Transactivator-mediated cytotoxicity depends on DNA binding, but can be overcome by BCL2 overexpression, suggesting that apoptosis in

SUBMITTER: Ottina E 

PROVIDER: S-EPMC5647323 | biostudies-literature | 2017 Oct

REPOSITORIES: biostudies-literature