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Originally published In Press as doi:10.1074/jbc.M700074200 on March 13, 2007

J. Biol. Chem., Vol. 282, Issue 18, 13542-13551, May 4, 2007
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RUNX1-RUNX1 Homodimerization Modulates RUNX1 Activity and Function*

Donglan Li1, Kislay K. Sinha1, Maher A. Hay, Ciro R. Rinaldi, Yogen Saunthararajah, and Giuseppina Nucifora2

From the Department of Medicine, University of Illinois, Chicago, Illinois 60612

RUNX1 (AML1, CBF{alpha}2, PEBP2{alpha}B) is a transcription factor essential for the establishment of the hematopoietic stem cell. It is generally thought that RUNX1 exists as a monomer that regulates hematopoietic differentiation by interacting with tissue-specific factors and its DNA consensus through its N terminus. RUNX1 is frequently altered in human leukemia by gene fusions or point mutations. In general, these alterations do not affect the N terminus of the protein, and it is unclear how they consistently lead to hematopoietic transformation and leukemia. Here we report that RUNX1 homodimerizes through a mechanism involving C terminus-C terminus interaction. This RUNX1-RUNX1 interaction regulates the activity of the protein in reporter gene assays and modulates its ability to induce hematopoietic differentiation of hematopoietic cell lines. The promoters of genes regulated by RUNX1 often contain multiple RUNX1 binding sites. This arrangement suggests that RUNX1 could homodimerize to bring and hold together distant chromatin sites and factors and that if the dimerization region is removed by gene fusions or is altered by point mutations, as observed in leukemia, the ability of RUNX1 to regulate differentiation could be impaired.


Received for publication, January 3, 2007 , and in revised form, March 9, 2007.

* This work was supported by National Institutes of Health R01 Grants HL72691, HL082935, HL79580, and CA96448 (to G. N.). The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked "advertisement" in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

1 Equal contributors.

2 To whom correspondence should be addressed: Dept. of Medicine, College of Medicine Research Bldg., M/C 737, University of Illinois at Chicago, 909 South Wolcott Ave., Chicago, IL 60612. Tel.: 312-413-4686; Fax: 312-413-0548; E-mail: nucifora{at}uic.edu.


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