Abstract

The homeobox gene Hox-2.4 is transcriptionally activated in cells of the mouse myeloid leukemia WEHI-3B. The constitutive Hox-2.4 expression in WEHI-3B cells is due to insertion of a transposable element belonging to the family of intracisternal A particles. In this study, we demonstrated the oncogenic potential of this activated homeobox gene. NIH 3T3 fibroblast clones bearing the activated Hox-2.4 gene produced fibrosarcomas in nude mice.

Highlights

  • We demonstrated the oncogenic potential of this activated homeobox gene

  • In our initial search for genomic changes of homeobox genes in tumor cells, we found a rearrangement of the Hox-2.4 gene in WEHI-3B mouse myeloid leukemia cells as a result of insertion of an intracisternal A particle (IAP) upstream of Hox-2.4 [4, 5]

  • All clones containing the IAP-Hox-2.4 gene expressed a high level of Hox-2.4 RNA, comparable to that in the WEHI-3B leukemic cells

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Summary

Introduction

The Oncogenic Potential of an Activated Hox-2.4 Homeobox Gene in Mouse Fibroblasts The homeobox gene Hox-2.4 is transcriptionally activated in cells of the mouse myeloid leukemia WEHI-3B. NIH 3T3 fibroblast clones bearing the activated Hox-2.4 gene produced fibrosarcomas in nude mice.

Results
Conclusion
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