cDNA cloning, tissue distribution, and chromosomal localization of myelodysplasia/myeloid leukemia factor 2 (MLF2)

Genomics

Volumn 35, Issue 2, 1996, Pages 392-396

  Kuefer, Martin U ^a   Look, A Thomas ^a,d   Williams, Deanna C ^a   Valentine, Virginia ^a   Naeve, Clayton W ^a,d   Behm, Frederick G ^a   Mullersman, Jerald E ^d   Yoneda Kato, Noriko ^b   Montgomery, Kate ^c   Kucherlapati, Raju ^c   Morris, Stephan W ^a,d  

^a ST JUDE CHILDREN S RESEARCH HOSPITAL   (United States)

^b KANSAI MEDICAL UNIVERSITY   (Japan)

^c ALBERT EINSTEIN COLLEGE OF MEDICINE   (United States)

^d UNIVERSITY OF TENNESSEE COLLEGE OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

MYELOID LEUKEMIA FACTOR 2; NUCLEOPHOSMIN; UNCLASSIFIED DRUG;

ARTICLE; CHROMOSOMAL LOCALIZATION; CHROMOSOME 12P; CHROMOSOME ANALYSIS; GENE REARRANGEMENT; HUMAN; HUMAN CELL; MOLECULAR CLONING; MYELODYSPLASIA; MYELOID LEUKEMIA; PRIORITY JOURNAL; TISSUE DISTRIBUTION;

EID: 0030586250     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1006/geno.1996.0376     Document Type: Article

References (19)

1. 1. Bairoch, A., and Bucher, P. (1994). PROSITE: Recent developments. Nucleic Acids Res. 22: 3583-3589.
2. KIP1. Blood 86: 3869-3875.
3. 3. Francke, U. (1994). Digitized and differentially shaded human chromosome ideograms for genomic applications. Cytogenet. Cell Genet. 65: 206-218.
4. 4. Garber, G. E., and Lemchuk-Favel, L. T. (1994). Analysis of the extracellular proteases of Trichomonas vaginalis. Parasitol. Res. 80: 361-365.
5. 5. Garber, G. E., Lemchuk-Favel, L. T., Meysick, K. C., and Dimock, K. (1993). A Trichomonas vaginalis cDNA with partial protein sequence homology with a Plasmodium falciparum excreted protein ABRA. Appl. Parasitol. 34: 245-249.
6. 6. Golub, T. R., Barker, G. F., Bohlander, S. K., Hiebert, S. W., Ward, D. C., Bray-Ward, P., Morgan, E., Raimondi, S. C., Rowley, J. D., and Gilliland, D. G. (1995). Fusion of the tel gene on 12p13 to the AML1 gene on 21q22 in acute lymphoblastic leukemia. Proc. Natl. Acad. Sci. USA 92: 4917-4921.
7. 7. Golub, T. R., Barker, G. F., Lovett, M., and Gilliland, D. G. (1994). Fusion of PDGF receptor beta to a novel ets-like gene, TEL, in chronic myelomonocytic leukemia with t(5;12) chromosomal translocation. Cell 77: 307-316.
8. 8. Henikoff, S., and Henikoff, J. G. (1994). Protein family classification based on searching a database of blocks. Genomics 19: 97-107.
9. 9. Kozak, M. (1987). An analysis of 5′-noncoding sequences from 699 vertebrate messenger RNAs. Nucleic Acids Res. 15: 8125-8148.
10. 10. Krauter, K., Montgomery, K., Yoon, S. J., LeBlanc-Straceski, J., Renault, B., Marondel, I., Herdman, V., Cupelli, L., Banks, A., Lieman, J., Menninger, J., Bray-Ward, P., Nadkarni, P., Weissenbach, J., Le Paslier, D., Rigault, P., Chumakov, I., Cohen, D., Miller, P., Ward, D., and Kucherlapati, R. (1995). A second-generation YAC contig map of human chromosome 12. Nature 377: 321-333.
11. 11. Look, A. T. (1995). Oncogenic role of "master" transcription factors in human leukemias and sarcomas: A developmental model. Adv. Cancer Res. 67: 25-57.
12. 12. Luthy, R., Xenarios, I., and Bucher, P. (1994). Improving the sensitivity of the sequence profile method. Protein Sci. 3: 139-146.
13. 13. Mitelman, F. (1994). "Catalog of Chromosome Aberrations in Cancer," Wiley-Liss, New York.
14. 14. Morris, S. W., Valentine, M. B., Shapiro, D. N., Sublett, J. E., Deaven, L. L., Foust, J. T., Roberts, W. M., Cerretti, D. P., and Look, A. T. (1991). Reassignment of the human CSF1 gene to chromosome 1p13-p21. Blood 78: 2013-2020.
15. 15. Papadopoulos, P., Ridge, S. A., Boucher, C. A., Stocking, C., and Wiedemann, L. M. (1995). The novel activation of ABL by fusion to an ets-related gene, TEL. Cancer Res. 55: 34-38.
16. Kip1, a cyclin-Cdk inhibitor, links transforming growth factor-β and contact inhibition to cell cycle arrest. Genes Dev. 8: 9-22.
17. 17. Raimondi, S. C., Williams, D. L., Callihan, T., Peiper, S., Rivera, G. K., and Murphy, S. B. (1986). Nonrandom involvement of the 12p12 breakpoint in chromosome abnormalities of childhood acute lymphoblastic leukemia. Blood 68: 69-75.
18. 18. Sato, Y., Suto, Y., Pietenpol, J., Golub, T. R., Gilliland, D. G., Davis, E. M., Le Beau, M. M., Roberts, J. M., Vogelstein, B., Rowley, J. D., and Bohlander, S. K. (1995). TEL and KIP1 define the smallest region of deletions on 12p13 in hematopoietic malignancies. Blood 86: 1525-1533.
19. 19. Yoneda-Kato, N., Look, A. T., Kirstein, M. N., Valentine, M. B., Raimondi, S. C., Cohen, K. J., Carroll, A. J., and Morris, S. W. (1996). The t(3;5)(q25.1;q34) of myelodysplastic syndrome and acute myeloid leukemia produces a novel fusion gene, NPM-MLF1. Oncogene 12: 265-275.