A novel positive tetracycline-dependent transactivator (rtTA) variant with reduced background activity and enhanced activation potential.

Abstract:

:The tetracycline-controlled transcription system has become one of the most potent systems for experimental manipulations of transcription levels in vivo. Here we report on rtTA variants, which were generated by combining the existing positively regulated Tet repressor domains of rtTA and rtTA-M2 with a modified and multimerized minimal transactivation domain from VP16 (L-domain). A transactivator with multimerized L-domains shows drastically reduced background activity and enhanced transcriptional activation on different tetracycline-responsive promoters. The new rtTA variants require higher doses of doxycycline and display a more linear dose-response curve than the original rtTA or rtTA-M2 proteins.

journal_name

FEBS Lett

journal_title

FEBS letters

authors

Kämper MR,Gohla G,Schlüter G

doi

10.1016/s0014-5793(02)02587-5

keywords:

subject

Has Abstract

pub_date

2002-04-24 00:00:00

pages

115-20

issue

1-3

eissn

0014-5793

issn

1873-3468

pii

S0014579302025875

journal_volume

517

pub_type

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