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A Novel Transgenic Mouse Model Reveals Humanlike Regulation of an 8-kbp Human TERT Gene Promoter Fragment in Normal and Tumor Tissues

¹ Heinrich-Pette-Institute, Department of Tumor Virology; ² University Hospital Hamburg, Institute of Tumor Biology, Hamburg, Germany; ³ Department of Pathology, University of Kiel, Kiel, Germany; and ⁴ Institute for Molecular Biotechnology, Jena, Germany

Requests for reprints: Cagatay Günes, Heinrich-Pette-Institute, Department of Tumor Virology, Martinistrasse 52, 20251 Hamburg, Germany. E-mail: Cagatay.Guenes{at}hpi.uni-hamburg.de.

Telomerase activity is repressed in most human somatic tissues during differentiation processes but strongly up-regulated in most human tumors. Regulation of human telomerase activity primarily occurs at the level of transcriptional initiation of the TERT gene, which encodes the catalytic subunit of telomerase. We have generated a novel transgenic mouse model to study the regulation of the human TERT gene promoter in an in vivo system. For this purpose, we have cloned an 8.0-kbp human TERT promoter fragment in front of the bacterial lacZ reporter gene (hTERTp-lacZ), which encodes the ß-galactosidase enzyme. Expression of the reporter gene was monitored by reverse transcription–PCR analysis, 5-bromo-4-chloro-3-indolyl-ß-D-galactopyranoside staining of whole mount preparations, and histologic sections. We find that the activity of the human TERT promoter in most normal mouse tissues recapitulates the expression of the hTERT gene in normal human tissues and is under tighter control when compared with the endogenous mouse TERT gene expression. In testis, where highest lacZ expression was observed, the expression of the reporter gene was restricted to the spermatogonial stem cells and the spermatocytes. Intriguingly, we find increased levels of lacZ expression in mammary tumors of hTERTp-lacZ x p53^+/– bitransgenic mouse mammary tumor model. Thus, this transgenic mouse model provides a suitable in vivo system to analyze the expression of the human TERT gene under physiologic conditions and during tumorigenesis.

Key Words: telomerase • testis • tumorigenesis • p53 • ß-galactosidase

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