Abstract
An expression vector containing the murine c-ets-2 protooncogene cDNA was introduced into NIH 3T3 cells by DNA transfection. The cells transfected with this construct showed foci of densely growing, morphologically altered cells, when grown either in low-serum (0.05%) or in serum-free medium. The c-ets-2-derived foci contained additional copies of the c-ets-2 gene, Northern blot analysis demonstrated overexpression of a c-ets-2-specific 2.5-kilobase RNA, and ets-specific antiserum recognized a 56-kDa protein. Overexpression of the c-ets-2-encoded protein stimulated cell proliferation and abolished their serum requirement. The c-ets-2 transfected cells formed colonies in semisolid medium and induced tumors in nude mice, indicating that c-ets-2 can be a transforming gene when overexpressed in these cells. This work demonstrates that a member of the c-ets gene family has transforming and mitogenic activity. In addition, the role of c-ets-2 in cell proliferation and its location in the minimal Down syndrome region on chromosome 21 implicates its involvement in the phenotypic changes associated with Down syndrome.
MeSH Terms
Animals
Blotting, Northern
Blotting, Southern
Cell Division
Cell Transformation, Neoplastic
Cells, Cultured
Genetic Vectors
Humans
Mice
Proto-Oncogenes/physiology
RNA, Messenger/genetics
Restriction Mapping
Transcription, Genetic
Transfection
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Seth A
Laboratory of Molecular Oncology, National Cancer Institute, Frederick, MD 21701-1013.
Watson D K
Blair D G
Papas T S
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