UMMS Affiliation

Department of Cancer Biology and the Cancer Center

Date

4-6-2006

Document Type

Article

Subjects

Animals; Base Sequence; Cell Cycle; Cell Transformation, Neoplastic; Gene Expression Regulation, Neoplastic; Green Fluorescent Proteins; HCT116 Cells; Hela Cells; Humans; Mice; Mice, Transgenic; Microtubule-Associated Proteins; Mitosis; Molecular Sequence Data; Promoter Regions (Genetics); Tumor Suppressor Protein p53

Disciplines

Cancer Biology | Genetics and Genomics

Abstract

Survivin is an essential mitotic gene, and this has been speculated to reflect its primary function in development and cancer. Here, we generated a knock-in transgenic mouse (SVVp-GFP) in which a green fluorescent protein (GFP) reporter gene was placed under the control of the survivin promoter that regulates transcription at mitosis. The expression of endogenous survivin was widespread in mouse tissues during development and shortly after birth. In contrast, GFP reactivity was undetectable in transgenic mouse embryos, and was largely limited postnatally to mitotic cells in the testes. Double transgenic mice generated in the tumor-prone Min/+ background exhibited intestinal adenomas that strongly expressed endogenous survivin, but only isolated GFP-positive cells. Conversely, dysplastic adenomas (16%) stained intensely for GFP, and revealed focal reactivity for mutant, but not wild-type, p53. The expression of GFP was increased by approximately 10-fold in p53(-/-) as opposed to p53(+/+) HCT116 colorectal cancer cells, and reintroduction of p53 in p53(-/-) cells abolished GFP expression. Therefore, the mitotic transcription of the survivin gene is highly restricted in vivo, and unexpectedly negatively regulated by p53. Contrary to a commonly held view, the dominant function(s) of survivin in development and tumor ontogeny are largely cell cycle-independent.

Rights and Permissions

Citation: Cancer Res. 2006 Apr 1;66(7):3392-5. Link to article on publisher's site

DOI of Published Version

10.1158/0008-5472.CAN-05-4537

Related Resources

Link to article in PubMed

Journal Title

Cancer research

PubMed ID

16585159

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