Aberrant cell growth induced by avian winged helix proteins

Cancer Research

Volumn 57, Issue 1, 1997, Pages 123-129

  Freyaldenhoven, Bettina S ^a   Freyaldenhoven, Markus P ^a   Iacovoni, Jason S ^a   Vogt, Peter K ^a  

^a SCRIPPS RESEARCH INSTITUTE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEMENTARY DNA; TRANSCRIPTION FACTOR;

ANCHORAGE INDEPENDENT GROWTH; ANIMAL CELL; ANIMAL TISSUE; ARTICLE; CELL GROWTH; CELL PROLIFERATION; CHICK EMBRYO; CONTROLLED STUDY; DNA BINDING; EMBRYO; FIBROBLAST; NONHUMAN; PRIORITY JOURNAL;

ANIMALS; AVIAN PROTEINS; BASE SEQUENCE; CELL COUNT; CELL DIFFERENTIATION; CELL DIVISION; CHICK EMBRYO; DNA-BINDING PROTEINS; FIBROBLASTS; GENETIC VECTORS; MOLECULAR SEQUENCE DATA; ONCOGENE PROTEINS; RNA, MESSENGER; SEQUENCE ANALYSIS, DNA; SEQUENCE HOMOLOGY, AMINO ACID; TRANSCRIPTION FACTORS; TRANSFECTION;

EID: 0031022788     PISSN: 00085472     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (46)

1. Lai, E., Clark, K. L., Burley, S. K., and Darnell, J. E., Jr. Hepatocyte nuclear factor 3/fork head or "winged helix" proteins: a family of transcription factors of diverse biologic function. Proc. Natl. Acad. Sci. USA, 90: 10421-10423, 1993.
2. Costa, R. H. Hepatocyte nuclear factor 3/forkhead protein family. In: F. Tronche and M. Yaniv (eds.), Liver-specific Gene Transcription, pp. 183-205. Boca Raton, FL: CRC Press, 1994.
3. Weigel, D., Jürgens, G., Küttner, F., Seifert, E., and Jäckle, H. The homeotic gene fork head encodes a nuclear protein and is expressed in the terminal regions of the Drosophila embryo. Cell, 57: 645-658, 1989.
4. Lai, E., Prezioso, V. R., Smith, E., Litvin, O., Costa, R. H., and Darnell, J. E., Jr. HNF-3A, a hepatocyte-enriched transcription factor of novel structure is regulated transcriptionally. Genes Dev., 4: 1427-1436, 1990.
5. Lai, E., Prezioso, V. R., Tao, W., Chen, W. S., and Darnell, J. E., Jr. Hepatocyte nuclear factor 3α belongs to a gene family in mammals that is homologous to the Drosophila homeotic gene fork head. Genes Dev., 5: 416-427, 1991.
6. Ang, S-L., and Rossant, J. HNF-3β is essential for node and notochord formation in mouse development. Cell, 78: 561-574, 1994.
7. Weinstein, D. C., Ruiz i Altaba, A., Chen, W. S., Hoodless, P., Prezioso, V. R., Jessell, T. M., and Darnell, J. E., Jr. The winged-helix transcription factor HNF-3β is required for notochord development in the mouse embryo. Cell, 78: 575-588, 1994.
8. Nehls, M., Pfeifer, D., Schorpp, M., Hedrich, H., and Boehm, T. New member of the winged-helix protein family disrupted in mouse and rat nude mutations. Nature (Lond.), 372: 103-106, 1994.
9. Clark, K. L., Halay, E. D., Lai, E., and Burley, S. K. Co-crystal structure of the HNF-3/fork head DNA-recognition motif resembles histone H5. Nature (Lond.), 364: 412-420, 1993.
10. Li, J., and Vogt, P. K. The retroviral oncogene qin belongs to the transcription factor family that includes the homeotic gene fork head. Proc. Natl. Acad. Sci. USA, 90: 4490-4494, 1993.
11. Chang, H. W., Li, J., Kretzschmar, D., and Vogt, P. K. Avian cellular homolog of the qin oncogene. Proc. Natl. Acad. Sci. USA, 92: 447-451, 1995.
12. Tao, W., and Lai, E. Telencephalon-restricted expression of BF-1, a new member of the HNF-3/fork head gene family, in the developing rat brain. Neuron, 8: 957-966, 1992.
13. Xuan, S., Baptista, C. A., Balas, G., Tao, W., Scares, V. C., and Lai, E. Winged helix transcription factor BF-1 is essential for the development of the cerebral hemispheres. Neuron, 14: 1141-1152, 1995.
14. Li, J., Chang, H. W., Lai, E., Parker, E. J., and Vogt, P. K. The oncogene qin codes for a transcriptional repressor. Cancer Res., 55: 5540-5544, 1995.
15. Hughes, S., an Kosik, E. Mutagenesis of the region between env and src of the SR-A strain of Rous sarcoma virus for the purpose of constructing helper-independent vectors. Virology, 136: 89-99, 1984.
16. Hughes, S. H., Greenhouse, J. J., Petropoulos, C. J., and Sutrave, P. Adaptor plasmids simplify the insertion of foreign DNA into helper-independent retroviral vectors. J. Virol., 61: 3004-3012, 1987.
17. Vogt, P. K. Focus assay of Rous sarcoma virus. In: K. Habel and N. P. Salzman (eds.), Fundamental Techniques in Virology, pp. 198-211. New York: Academic Press, 1969.
18. Kawai, S., and Nishizawa, M. New procedure for DNA transfection with polycation and dimethyl sulfoxide. Mol. Cell. Biol., 4: 1172-1174, 1984.
19. Bos, T. J., Monteclaro, F. S., Mitsunobu, F., Ball, A. R., Jr., Chang, C. H. W., Nishimura, T., and Vogt, P. K. Efficient transformation of chicken embryo fibroblasts by c-Jun requires structural modification in coding and noncoding sequences. Genes Dev., 4: 1677-1687, 1990.
20. Bister, K., Hayman, M. J., and Vogt, P. K. Defectiveness of avian myelocytomatosis virus MC29: isolation of long-term nonproducer cultures and analysis of virus-specific polypeptide synthesis. Virology, 82: 431-448, 1977.
21. Connolly, D. T., Knight, M. B., Harakas, N. K., Wittwer, A. J., and Feder, J. Determination of the number of endothelial cells in culture using an acid phosphatase assay. Anal. Biochem., 152, 136-140, 1986.
22. Niman, H. L., Houghten, R. A., Walker, L. E., Reisfeld, R. A., Wilson, I. A., Hogle, J. M., and Lerner, R. A. Generation of protein-reactive antibodies by short peptides is an event of high frequency: implications for the structural basis of immune recognition. Proc. Natl. Acad. Sci. USA, 80: 4949-4953, 1983.
23. Kozak, M. An analysis of 5′-noncoding sequences from 699 vertebrate messenger RNAs. Nucleic Acids Res., 15: 8125-8132, 1987.
24. Mitchell, P. J., and Tjian, R. Transcriptional regulation in mammalian cells by sequence-specific DNA binding proteins. Science (Washington DC), 245: 371-378, 1989.
25. Pani, L., Overdier, D. G., Porcella, A., Qian, X., Lai, E., and Costa, R. H. Hepatocyte nuclear factor 3β contains two transcriptional activation domains, one of which is novel and conserved with the Drosophila fork head protein. Mol. Cell. Biol., 12: 3723-3732, 1992.
26. Hatini, V., Tao, W., and Lai, E. Expression of winged helix genes, BF-1 and BF-2, define adjacent domains within the developing forebrain and retina. J. Neurobiol., 25: 1293-1309, 1994.
27. Clevidence, D. E., Overdier, D. G., Tao, W., Qian, X., Pani, L., Lai, E., and Costa, R. H. Identification of nine tissue-specific transcription factors of the hepatocyte nuclear factor 3/forkhead DNA-binding-domain family. Proc. Natl. Acad. Sci. USA, 90: 3948-3952, 1993.
28. Pierrou, S., Hellqvist, M. Samuelsson, L., Enerbäck, S., and Carlsson, P. Cloning and characterization of seven human forkhead proteins: binding site specificity and DNA bending. EMBO J., 13: 5002-5012, 1994.
29. Miura, N., Wanaka, A., Tohyama, M., and Tanaka, K. MFH-1, a new member of the fork head domain family, is expressed in developing mesenchyme. FEBS Lett., 326: 171-176, 1993.
30. Costa, R. H., Grayson, D. R., and Darnell, J. E., Jr. Multiple hepatocyte-enriched nuclear factors function in the regulation of transthyretin and α1-antitrypsin genes. Mol. Cell. Biol., 9: 1415-1425, 1989.
31. Kuo, C. J., Conley, P. B., Chen, L., Sladek, F. M., Darnell, J. E., Jr., and Crabtree, G. R. A transcriptional hierarchy involved in mammalian cell-type specification. Nature (Lond.), 355: 457-461, 1992.
32. Overdier, D. G., Porcella, A., and Costa, R. H. The DNA-binding specificity of the hepatocyte nuclear factor 3/forkhead domain is influenced by amino acid residues adjacent to the recognition helix. Mol. Cell. Biol., 14: 2755-2766, 1994.
33. Kamps, M. P., and Baltimore, D. E2A-Pbx1, the t(1;19) translocation protein of human pre-B-cell acute lymphocytic leukemia, causes acute myeloid leukemia in mice. Mol. Cell. Biol., 13: 351-357, 1993.
34. Lu, Q, Wright, D. D., and Kamps, M. P. Fusion with E2A converts the Pbx1 homeodomain protein into a constitutive transcriptional activator in human leukemias carrying the t(1;19) translocation. Mol. Cell. Biol., 14: 3938-3948, 1994.
35. Meyers, S., Downing, J. R., and Hiebert, S. W. Identification of AML-1 and the (8;21) translocation protein (AML-1/ETO) as sequence-specific DNA-binding proteins: the runt homology domain is required for DNA binding and protein-protein interactions. Mol. Cell. Biol., 13: 6336-6345, 1993.
36. Gu, Y., Nakamura, T., Alder, H., Prasad, R., Canaani, O., Cimino, G., Croce, C. M., and Canaani, E. The t(4;11) chromosome translocation of human acute leukemias fuses the ALL-1 gene, related to Drosophila trithorax, to the AF-4 gene. Cell, 71: 701-708, 1992.
37. Ma, Q., Alder, H., Nelson, K. K., Chatterjee, D., Gu, Y., Nakamura, T., Canaani, E., Croce, C. M., Siracusa, L. D., and Buchberg, A. M. Analysis of the murine All-1 gene reveals conserved domains with human ALL-1 and identifies a motif shared with DNA methyltransferases. Proc. Natl. Acad. Sci. USA, 90: 6350-6354, 1993.
38. Schichman, S. A., Caligiuri, M. A., Gu, Y., Strout, M. P., Canaani, E., Bloomfield, C. D., and Croce, C. M. All-1 partial duplication in acute leukemia. Proc. Natl. Acad. Sci. USA, 91: 6236-6239, 1994.
39. McCabe, N. R., Kipiniak, M., Kobayashi, H., Thirman, M., Gill, H., Rowley, J. D., and Diaz, M. O. DNA rearrangements and altered transcripts of the MLL gene in a human T-ALL cell line Karpas 45 with a t(X;11) (q13;q23) translocation. Genes Chromosomes & Cancer, 9: 221-224, 1994.
40. Djabali, M., Selleri, L., Parry, P., Bower, M., Young, B., and Evans, G. A. A trithorax-like gene is interrupted by chromosome 11q23 translocations in acute leukaemias. Nat. Genet., 2: 113-118, 1992.
41. McCabe, N. R., Burnett, R. C., Gill, H. J., Thirman, M. J., Mbangkollo, D., Kipiniak, M., van Melle, E., Ziemin-Van Der Poel, S., Rowley, J. D., and Diaz, M. O. Cloning of cDNAs of the MLL gene that detect DNA rearrangements and altered RNA transcripts in human leukemic cells with 11q23 translocations. Proc. Natl. Acad. Sci. USA, 89: 11794-11798, 1992.
42. Kennedy, M. A., Gonzalez-Sarmiento, R., Kees, U. R., Lampert, F., Dear, N., Boehm, T., and Rabbitts, T. H, HOX11, a homeobox-containing T-cell oncogene on human chromosome 10q24. Proc. Natl. Acad. Sci. USA, 88: 8900-8904, 1991.
43. Parry, P., Wei, Y., and Evans, G. Cloning and characterization of the t(X;11) breakpoint from a leukemic cell line identify a new member of the forkhead gene family. Genes Chromosomes & Cancer, 11: 79-84, 1994.
44. Shapiro, D. N., Sublett, J. E., Li, B., Downing, J. R., and Naeve, C. W. Fusion of PAX3 to a member of the forkhead family of transcription factors in human alveolar rhabdomyosarcoma. Cancer Res., 53: 5108-5112, 1993.
45. Galili, N., Davis, R. J., Fredericks, W. J., Mukhopadhyay, S., Rauscher, F. J., III, Emanuel, B. S., Rovera, G., and Barr, F. G. Fusion of a fork head domain gene to PAX3 in the solid tumour alveolar rhabdomyosarcoma. Nat. Genet., 5: 230-235, 1993.
46. Fredericks, W. J., Galili, N., Mukhopadhyay, S., Rovera, G., Bennicelli, J., Barr, F. G., and Rauscher, F. J., III. The PAX3-FKHR fusion protein created by the t(2;13) translocation in alveolar rhabdomyosarcomas is a more potent transcriptional activator than PAX3. Mol. Cell. Biol., 15: 1522-1535, 1995.