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Table 1 Comparison of features between the constitutive MMTV-PyV mT/MMTV-Cre recombinase model and the inducible MMTV-rtTA/TetO-MIC model

From: Inducible and coupled expression of the polyomavirus middle T antigen and Cre recombinase in transgenic mice: an in vivo model for synthetic viability in mammary tumour progression

 

MMTV-PyV mT/MMTV-Cre recombinase

MMTV-rtTA/TetO-MIC

(rtTA/MIC [+Dox])

PyV mT transgene promoter

Mouse mammary tumour virus (MMTV)

Tetracycline operator (TetO)

Inducible transgene expression

No

Yes

Coupling to Cre recombinase

No

Yes

Time when 50% of animals have tumours (T 50 )

40 days of age [6]

7 days of induction

Tumour pathology

Solid adenocarcinoma [3, 4]

Solid adenocarcinoma

Cre recombinase expression and function in PyV mT tumour cells (by X-gal assay)

0% when conditional gene is essential for tumourigenesis [5–7]

100%

Percentage of tumour-bearing mice with lung metastases

93.3% [6]

100%