» Articles » PMID: 26555930

Tet-on, or Tet-off, That is the Question: Advanced Conditional Gene Expression in Aspergillus

Overview
Date 2015 Nov 12
PMID 26555930
Citations 51
Authors
Affiliations
Soon will be listed here.
Abstract

In Aspergillus, controlled gene expression is often achieved using the reverse tetracycline-controlled transactivator (rtTA) dependent Tet-on system, whereby transcription is activated in a titratable manner by addition of the tetracycline derivative doxycycline. The complementary Tet-off system utilises the tetracycline-controlled transactivator (tTA) component to quantitatively reduce gene expression. In this study, we utilised a synthetic biological approach to engineer highly optimised Tet-off conditional expression systems in Aspergillus niger and Aspergillus fumigatus. Steps for delivery of these tools include utilising codon optimised cassette components, testing several promoters for improved genetic stability and validating two modified luciferase reporters for highly accurate measurements of gene expression. The Tet-off cassettes developed in this study enable facile and quantitative functional analysis, as validated by Tet-off analysis of genes involved in chitin synthesis and cell wall polarity in A. niger, and para-aminobenzoic acid synthesis in A. fumigatus. We also used a racA(G18V) dominant allele to demonstrate that Tet-off in A. niger enables gene over-expression and downregulation in a single isolate. Additionally, we used the improved luciferase reporters to show that the Tet-off cassette in A. niger enables quantification of gene oscillations. In order to demonstrate that synthetic biological approaches developed here are broadly applicable to engineering transcriptional circuits in filamentous fungi, we used our strategy for improving cassette stability by promoter replacement in the A. niger Tet-on system, which resulted in a modified Tet-on cassette with higher stability in recipient genomes.

Citing Articles

The antifungal peptide AnAFP from promotes nutrient mobilization through autophagic recycling during asexual development.

Starke S, Velleman L, Dobbert B, Seibert L, Witte J, Jung S Front Microbiol. 2025; 15:1490293.

PMID: 39925883 PMC: 11802824. DOI: 10.3389/fmicb.2024.1490293.


The sulfur-related metabolic status of during infection reveals cytosolic serine hydroxymethyltransferase as a promising antifungal target.

Alharthi R, Sueiro-Olivares M, Storer I, Bin Shuraym H, Scott J, Al-Shidhani R Virulence. 2025; 16(1):2449075.

PMID: 39825596 PMC: 11749473. DOI: 10.1080/21505594.2024.2449075.


Promoter engineering with programmable upstream activating sequences in Aspergillus Niger cell factory.

Zheng X, Guo Y, Chen M, Lu Y, Du Y, Lei Y Microb Cell Fact. 2025; 24(1):20.

PMID: 39815338 PMC: 11734539. DOI: 10.1186/s12934-025-02642-y.


A conserved fungal morphogenetic kinase regulates pathogenic growth in response to carbon source diversity.

Martin-Vicente A, Souza A, Guruceaga X, Thorn H, Xie J, Nywening A Nat Commun. 2024; 15(1):8945.

PMID: 39414804 PMC: 11484838. DOI: 10.1038/s41467-024-53358-3.


The Tet-on system for controllable gene expression in the rock-inhabiting black fungus Knufia petricola.

Erdmann E, Brandhorst A, Gorbushina A, Schumacher J Extremophiles. 2024; 28(3):38.

PMID: 39105933 PMC: 11303440. DOI: 10.1007/s00792-024-01354-2.