Abstract

Myeloid ELF1-like factor (MEF/ELF4), a member of the ETS transcription factors, can function as an oncogene in murine cancer models and is overexpressed in various human cancers. Here, we report a mechanism by which MEF/ELF4 may be activated by a common leukemia-associated mutation in the nucleophosmin gene. By using a tandem affinity purification assay, we found that MEF/ELF4 interacts with multifactorial protein nucleophosmin (NPM1). Coimmunoprecipitation and GST pull-down experiments demonstrated that MEF/ELF4 directly forms a complex with NPM1 and also identified the region of NPM1 that is responsible for this interaction. Functional analyses showed that wild-type NPM1 inhibited the DNA binding and transcriptional activity of MEF/ELF4 on the HDM2 promoter, whereas NPM1 mutant protein (Mt-NPM1) enhanced these activities of MEF/ELF4. Induction of Mt-NPM1 into MEF/ELF4-overexpressing NIH3T3 cells facilitated malignant transformation. In addition, clinical leukemia samples with NPM1 mutations had higher human MDM2 (HDM2) mRNA expression. Our data suggest that enhanced HDM2 expression induced by mutant NPM1 may have a role in MEF/ELF4-dependent leukemogenesis.

Highlights

  • We report a mechanism by which MEF/ELF4 may be activated by a common leukemia-associated mutation in the nucleophosmin gene

  • By using a tandem affinity purification assay, we found that MEF/ELF4 interacts with multifactorial protein nucleophosmin (NPM1)

  • Functional analyses showed that wild-type NPM1 inhibited the DNA binding and transcriptional activity of MEF/ELF4 on the human MDM2 (HDM2) promoter, whereas NPM1 mutant protein (Mt-NPM1) enhanced these activities of MEF/ELF4

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Summary

Conclusion

MEF/ELF4 activity may be activated by NPM1 mutant protein. Significance: NPM1 mutant proteins have a role in MEF/ELF4-dependent leukemogenesis. Myeloid ELF1-like factor (MEF/ELF4), a member of the ETS transcription factors, can function as an oncogene in murine cancer models and is overexpressed in various human cancers. Induction of Mt-NPM1 into MEF/ELF4-overexpressing NIH3T3 cells facilitated malignant transformation. Our data suggest that enhanced HDM2 expression induced by mutant NPM1 may have a role in MEF/ ELF4-dependent leukemogenesis. We found that wild-type NPM1 (WtNPM1) down-regulates, whereas mutated NPM1 (Mt-NPM1) up-regulates, the transcriptional activity of MEF/ELF4 on the human MDM2 (HDM2) promoter. The expression of MtNPM1 in MEF/ELF4-overexpressing NIH3T3 cells resulted in enhanced malignant transformation. Our data suggest that NPM1 mutations may promote transformation by enhancing the oncogenic functions of MEF/ELF4

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