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Originally published In Press as doi:10.1074/jbc.M110392200 on December 18, 2001
J. Biol. Chem., Vol. 277, Issue 10, 8566-8571, March 8, 2002
Interaction and Cooperation of mi Transcription
Factor (MITF) and Myc-associated Zinc-finger Protein-related Factor
(MAZR) for Transcription of Mouse Mast Cell Protease 6 Gene*
Eiichi
Morii §,
Keisuke
Oboki ,
Tatsuki R.
Kataoka ,
Kazuhiko
Igarashi¶, and
Yukihiko
Kitamura
From the Department of Pathology (Room C2), Osaka
University Medical School, 2-2 Yamada-oka, Suita, Osaka, 565-0871, Japan, and the ¶ Department of Biochemistry, Hiroshima University
Medical School, 1-2-3 Kasumi, Minami-ku, Hiroshima 734-8551, Japan
The mi transcription factor (MITF) is
a basic-helix-loop-helix leucine zipper (bHLH-Zip) transcription factor
that is important for the normal phenotypic expression of mast cells.
Most transcription factors function in cooperation with other factors
by protein-protein interactions. To search proteins interacting with
MITF, we carried out a yeast two-hybrid screen and isolated
Myc-associated zinc-finger protein related factor (MAZR) as a
partner of MITF. When expressed with MITF in NIH/3T3 cells, MAZR was
colocalized with MITF. The association of MAZR with MITF was further
confirmed by a co-immunoprecipitation study and in vitro
binding assay. The zinc-finger domain of MAZR and the Zip domain of
MITF were essential for the interaction. MAZR was expressed in cultured
mast cells and MST mastocytoma cells containing mouse mast cell
protease (mMCP)-6 transcript abundantly. The overexpression of dominant
negative MAZR in MST mastocytoma cells reduced the amount of mMCP-6
mRNA. The simultaneous transfection of MAZR and MITF significantly
increased the promoter activity of the mMCP-6 gene, indicating
that the MAZR and MITF synergistically transactivated the mMCP-6 gene.
MAZR appeared to play important roles in the normal phenotypic
expression of mast cells in association with MITF.
*
This work was supported by grants from the Ministry of
Education, Culture, Sports, Science, and Technology and the Uehara Memorial Foundation.The costs of publication of this
article were defrayed in part by the
payment of page charges. The article
must therefore be hereby marked
"advertisement" in
accordance with 18 U.S.C. Section
1734 solely to indicate this fact.
§
To whom correspondence should be addressed. Tel.: 81-6-6879-3721;
Fax: 81-6-6879-3729, E-mail: morii@patho.med.osaka-u.ac.jp.
Copyright © 2002 by The American Society for Biochemistry and Molecular Biology, Inc.

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Copyright © 2002 by the American Society for Biochemistry and Molecular Biology.
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