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A transcriptional hierarchy involved in mammalian cell-type specification

Abstract

ALTHOUGH transcriptional hierachies have been extensively studied in invertebrates, their involvement in mammalian cell-type specification is poorly understood1,2. Here we report a hepatocyte transcriptional cascade suggested by the expression patterns of hepatic transcription factors in dedifferentiated hepatomas and hepatocyte: fibroblast hybrids in which the liver phenotype was extinguished3–6. These results indicated that the homeoprotein hepatocyte nuclear factor-lα (HNF-lα)7–8, and HNF-4, a member of the steroid hormone receptor superfamily9, were regulated coordinately or in a hierarchy by a higher-order locus, independently of other hepatic transactivators. HNF-4 was implicated as an essential positive regulator of HNF-lα, as deletion of an HNF-4 binding site in the HNF-lα promoter abolished promoter activity, and HNF-4→ potently transactivated the HNF-lα promoter in cotransfection assays. Moreover, genetic complementation of dedifferentiated hepatomas with HNF-4 complementary DNA rescued expression of endogenous HNF-lα messenger RNA and DNA-binding activity. Our studies therefore define an HNF-4→ HNF-1 α (4 -→ 1α) transcriptional hierarchy operative in differentiated hepatocytes but selectively inhibited by an extinguishing locus and somatic mutations which antagonize the liver phenotype.

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References

  1. Winslow, G. M., Hayashi, S., Krasnow, M., Hogness, D. S. & Scott, M. P. Cell. 57, 1017–1030 (1989).

    Article  CAS  Google Scholar 

  2. Hayashi, H. & Scott, M. P. Cell 63, 883–894 (1990).

    Article  CAS  Google Scholar 

  3. Deschatrette, J. & Weiss, M. C. Biochimie 56, 1603–1611 (1974).

    Article  CAS  Google Scholar 

  4. Deschatrette, J., Moore, E. E., Dubois, M. & Weiss, M. Cell 19, 1043–1051 (1980).

    Article  CAS  Google Scholar 

  5. Killary, A. M. & Fournier, R. E. K. Cell 38, 523–534 (1984).

    Article  CAS  Google Scholar 

  6. Chin, S. C. & Fournier, R. E. K. Molec. cell. Biol. 9, 3736–3743 (1989).

    Article  CAS  Google Scholar 

  7. Frain, M. et al. Cell 59, 1179–1187 (1989).

    Article  Google Scholar 

  8. Baumhueter, S. et al. Genes Dev. 4, 372–379 (1990).

    Article  CAS  Google Scholar 

  9. Sladek, F. M., Zhong, W., Lai, E. & Darnell, J. E. Genes Dev. 4, 2353–2365 (1991).

    Article  Google Scholar 

  10. Baumhueter, S., Courtois, G. & Crabtree, G. R. EMBO J. 7, 2485–2493 (1988).

    Article  CAS  Google Scholar 

  11. Cereghini, S., Blumenfeld, M. & Yaniv, M. Genes Dev. 8, 957–974 (1988).

    Article  Google Scholar 

  12. Cereghini, S., Yaniv, M. & Cortese, R. EMBO J. 9, 2257–2263 (1990).

    Article  CAS  Google Scholar 

  13. Herbst, R. S. et al. New Biol. 3, 289–296 (1991).

    CAS  PubMed  Google Scholar 

  14. Kuo, C. J., Conley, P. B., Hsieh, C., Franke, U. & Crabtree, G. R. Proc. natn. Acad. Sci. U.S.A. 87, 9838–9842 (1990).

    Article  ADS  CAS  Google Scholar 

  15. Courtois, G., Morgan, J. G., Campbell, L. A., Fourel, G. & Crabtree, G. R. Science 238, 688–692 (1987).

    Article  ADS  CAS  Google Scholar 

  16. De Simone, V. et al. EMBO J. 10, 1435–1443 (1991).

    Article  CAS  Google Scholar 

  17. Lai, E., Prezioso, V. R., Tao, W., Chen, W. S., & Darnell, J. E. Genes Dev. 5, 416–427 (1991).

    Article  CAS  Google Scholar 

  18. Lai, E. et al. Genes Dev. 4, 1427–1436 (1990).

    Article  CAS  Google Scholar 

  19. Chiu, R. et al. Cell 54, 541–552 (1988).

    Article  CAS  Google Scholar 

  20. McCormick, A., Brady, H., Theill, L. E. & Karin, M. Nature 345, 829–832 (1990).

    Article  ADS  CAS  Google Scholar 

  21. Chen, R. et al. Nature 346, 583–586 (1990).

    Article  ADS  CAS  Google Scholar 

  22. Tsai, S.-F., Strauss, E. & Orkin, S. H. Genes Dev. 5, 919–931 (1991).

    Article  CAS  Google Scholar 

  23. Tonjes, R. R., Xanthopoulos, K. G., Darnell, J. E. Jr & Paul, D. EMBO J. (in the press).

  24. Gourdeau, H. & Fournier, R. E. K. A. Rev. Cell Biol. 6, 69–94 (1990).

    Article  CAS  Google Scholar 

  25. Kuo, C. J., Mendel, D. B., Hansen, L. P. & Crabtree, G. R. EMBO J. 10, 2231–2236 (1991).

    Article  CAS  Google Scholar 

  26. Mendel, D. B., Hansen, L. P., Graves, M. K., Conley, P. B. & Crabtree, G. R. Genes Dev. 5, 1042–1056 (1991).

    Article  CAS  Google Scholar 

  27. Lichtsteiner, S., Wuarin, J. & Schibler, U. Cell 51, 963–973 (1987).

    Article  CAS  Google Scholar 

  28. Emmel, E. A. et al. Science 246, 1617–1620 (1989).

    Article  ADS  CAS  Google Scholar 

  29. Ho, S. N., Hunt, H. D., Horton, R. M., Pullen, J. K. & Pease, L. R. Gene 77, 51–59 (1989).

    Article  CAS  Google Scholar 

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Kuo, C., Conley, P., Chen, L. et al. A transcriptional hierarchy involved in mammalian cell-type specification. Nature 355, 457–461 (1992). https://doi.org/10.1038/355457a0

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