Previous Article | Next Article 
Mol Cell Biol, July 1998, p. 4252-4261, Vol. 18, No. 7
0270-7306/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Cytoplasmic Sequestration of the Polyomavirus Enhancer Binding
Protein 2 (PEBP2)/Core Binding Factor
(CBF
) Subunit by
the Leukemia-Related PEBP2/CBF
-SMMHC Fusion Protein
Inhibits PEBP2/CBF-Mediated Transactivation
Yuka
Kanno,
Tomohiko
Kanno,
Chohei
Sakakura,
Suk-Chul
Bae, and
Yoshiaki
Ito*
Department of Viral Oncology, Institute for
Virus Research, Kyoto University, Kyoto 606, Japan
Received 4 March 1998/Returned for modification 7 April
1998/Accepted 21 April 1998
The polyomavirus enhancer binding protein 2 (PEBP2)/core binding
factor (CBF) is a transcription factor composed of two subunits,
and
. The gene encoding the
subunit is disrupted by inv(16), resulting in the formation of a chimeric protein,
-SMMHC, which is
associated with acute myelogenous leukemia. To understand the effect of
-SMMHC on PEBP2-mediated transactivation, we used a luciferase assay system in which contribution of both the
and
subunits was absolutely required to activate transcription. Using this
system, we found that the minimal region of the
subunit required
for transactivation resides between amino acid 1 and 135, which is
known to dimerize with the
subunit. In contrast,
-SMMHC, despite
having this minimal region for dimerization and transactivation, failed
to support transcription with the
subunit. Furthermore
-SMMHC
blocked the synergistic transcription achieved by PEBP2 and
CCAAT/enhancer binding protein
. By using a construct in which the
PEBP2
subunit was fused to the glucocorticoid receptor ligand
binding domain, we demonstrated that coexpressed
-SMMHC tightly
sequestered the
subunit in the cytoplasm and blocked dexamethasone-dependent nuclear translocation of the
subunit. Thus,
the result suggess that
-SMMHC inhibits PEBP2-mediated transcription via cytoplasmic sequestration of the
subunit. Lastly proliferation of ME-1 cells that harbor inv(16) was blocked by an antisense oligonucleotide complementary to the junction of the
chimeric mRNA, suggesting that
-SMMHC contributes to leukemogenesis by blocking the differentiation of myeloid cells.
*
Corresponding author. Mailing address: Institute for
Virus Research, Kyoto University, Shogo-in, Sakyo-ku, Kyoto 606, Japan. Phone: 81-75-751-4028. Fax: 81-75-752-3232. E-mail:
yito{at}virus.kyoto-u.ac.jp.
Mol Cell Biol, July 1998, p. 4252-4261, Vol. 18, No. 7
0270-7306/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
This article has been cited by other articles:
-
Wee, H.-J., Voon, D. C.-C., Bae, S.-C., Ito, Y.
(2008). PEBP2-{beta}/CBF-{beta}-dependent phosphorylation of RUNX1 and p300 by HIPK2: implications for leukemogenesis. Blood
112: 3777-3787
[Abstract]
[Full Text]
-
Markus, J., Garin, M. T., Bies, J., Galili, N., Raza, A., Thirman, M. J., Le Beau, M. M., Rowley, J. D., Liu, P. P., Wolff, L.
(2007). Methylation-Independent Silencing of the Tumor Suppressor INK4b (p15) by CBF{beta}-SMMHC in Acute Myelogenous Leukemia with inv(16). Cancer Res.
67: 992-1000
[Abstract]
[Full Text]
-
Frohling, S., Scholl, C., Gilliland, D. G., Levine, R. L.
(2005). Genetics of Myeloid Malignancies: Pathogenetic and Clinical Implications. JCO
23: 6285-6295
[Abstract]
[Full Text]
-
Helbling, D., Mueller, B. U., Timchenko, N. A., Schardt, J., Eyer, M., Betts, D. R., Jotterand, M., Meyer-Monard, S., Fey, M. F., Pabst, T.
(2005). CBFB-SMMHC is correlated with increased calreticulin expression and suppresses the granulocytic differentiation factor CEBPA in AML with inv(16). Blood
106: 1369-1375
[Abstract]
[Full Text]
-
Yang, G., Khalaf, W., van de Locht, L., Jansen, J. H., Gao, M., Thompson, M. A., van der Reijden, B. A., Gutmann, D. H., Delwel, R., Clapp, D. W., Hiebert, S. W.
(2005). Transcriptional Repression of the Neurofibromatosis-1 Tumor Suppressor by the t(8;21) Fusion Protein. Mol. Cell. Biol.
25: 5869-5879
[Abstract]
[Full Text]
-
Huang, G., Shigesada, K., Wee, H.-J., Liu, P. P., Osato, M., Ito, Y.
(2004). Molecular basis for a dominant inactivation of RUNX1/AML1 by the leukemogenic inversion 16 chimera. Blood
103: 3200-3207
[Abstract]
[Full Text]
-
Harada, H., Harada, Y., Niimi, H., Kyo, T., Kimura, A., Inaba, T.
(2004). High incidence of somatic mutations in the AML1/RUNX1 gene in myelodysplastic syndrome and low blast percentage myeloid leukemia with myelodysplasia. Blood
103: 2316-2324
[Abstract]
[Full Text]
-
Durst, K. L., Lutterbach, B., Kummalue, T., Friedman, A. D., Hiebert, S. W.
(2003). The inv(16) Fusion Protein Associates with Corepressors via a Smooth Muscle Myosin Heavy-Chain Domain. Mol. Cell. Biol.
23: 607-619
[Abstract]
[Full Text]
-
Kummalue, T., Lou, J., Friedman, A. D.
(2002). Multimerization via Its Myosin Domain Facilitates Nuclear Localization and Inhibition of Core Binding Factor (CBF) Activities by the CBF{beta}-Smooth Muscle Myosin Heavy Chain Myeloid Leukemia Oncoprotein. Mol. Cell. Biol.
22: 8278-8291
[Abstract]
[Full Text]
-
Kundu, M., Chen, A., Anderson, S., Kirby, M., Xu, L., Castilla, L. H., Bodine, D., Liu, P. P.
(2002). Role of Cbfb in hematopoiesis and perturbations resulting from expression of the leukemogenic fusion gene Cbfb-MYH11. Blood
100: 2449-2456
[Abstract]
[Full Text]
-
Michaud, J., Wu, F., Osato, M., Cottles, G. M., Yanagida, M., Asou, N., Shigesada, K., Ito, Y., Benson, K. F., Raskind, W. H., Rossier, C., Antonarakis, S. E., Israels, S., McNicol, A., Weiss, H., Horwitz, M., Scott, H. S.
(2002). In vitro analyses of known and novel RUNX1/AML1 mutations in dominant familial platelet disorder with predisposition to acute myelogenous leukemia: implications for mechanisms of pathogenesis. Blood
99: 1364-1372
[Abstract]
[Full Text]
-
Kaminker, J. S., Singh, R., Lebestky, T., Yan, H., Banerjee, U.
(2001). Redundant function of Runt Domain binding partners, Big brother and Brother, during Drosophila development. Development
128: 2639-2648
[Abstract]
[Full Text]
-
Miller, J. D., Stacy, T., Liu, P. P., Speck, N. A.
(2001). Core-binding factor {beta} (CBF{beta}), but not CBF{beta}-smooth muscle myosin heavy chain, rescues definitive hematopoiesis in CBF{beta}-deficient embryonic stem cells. Blood
97: 2248-2256
[Abstract]
[Full Text]
-
Strom, D. K., Nip, J., Westendorf, J. J., Linggi, B., Lutterbach, B., Downing, J. R., Lenny, N., Hiebert, S. W.
(2000). Expression of the AML-1 Oncogene Shortens the G1 Phase of the Cell Cycle. J. Biol. Chem.
275: 3438-3445
[Abstract]
[Full Text]
-
Lutterbach, B., Hou, Y., Durst, K. L., Hiebert, S. W.
(1999). The inv(16) encodes an acute myeloid leukemia 1 transcriptional corepressor. Proc. Natl. Acad. Sci. USA
96: 12822-12827
[Abstract]
[Full Text]
-
Lowenberg, B., Downing, J. R., Burnett, A.
(1999). Acute Myeloid Leukemia. NEJM
341: 1051-1062
[Full Text]
-
Osato, M., Asou, N., Abdalla, E., Hoshino, K., Yamasaki, H., Okubo, T., Suzushima, H., Takatsuki, K., Kanno, T., Shigesada, K., Ito, Y.
(1999). Biallelic and Heterozygous Point Mutations in the Runt Domain of the AML1/PEBP2alpha B Gene Associated With Myeloblastic Leukemias. Blood
93: 1817-1824
[Abstract]
[Full Text]
-
Li, L., Gergen, J.
(1999). Differential interactions between Brother proteins and Runt domain proteins in the Drosophila embryo and eye. Development
126: 3313-3322
[Abstract]
-
Kogan, S. C., Lagasse, E., Atwater, S., Bae, S.-c., Weissman, I., Ito, Y., Bishop, J. M.
(1998). The PEBP2beta MYH11 fusion created by Inv(16)(p13;q22) in myeloid leukemia impairs neutrophil maturation and contributes to granulocytic dysplasia. Proc. Natl. Acad. Sci. USA
95: 11863-11868
[Abstract]
[Full Text]