Effect of a large deletion of the basic domain of mi transcription factor on differentiation of mast cells

被引:18
作者
Morii, E
Ogihara, H
Oboki, K
Kataoka, TR
Maeyama, K
Fisher, DE
Lamoreux, ML
Kitamura, Y
机构
[1] Osaka Univ, Sch Med, Dept Pathol, Suita, Osaka 5650871, Japan
[2] Ehime Univ, Sch Med, Dept Pharmacol, Matsuyama, Ehime 790, Japan
[3] Harvard Univ, Sch Med, Dana Farber Canc Inst, Div Pediat Hematol Oncol, Boston, MA 02115 USA
[4] Harvard Univ, Sch Med, Childrens Hosp, Boston, MA 02115 USA
[5] Texas A&M Univ, Dept Vet Pathobiol, College Stn, TX USA
关键词
D O I
10.1182/blood.V98.8.2577
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The mi transcription factor (MITF) is a basic-helix-loop-helix-leucine zipper transcription factor that is important for the development of mast cells. Cultured mast cells (CMCs) of mi/mi genotype express abnormal MITF (mi-MITF), but CMCs of tg/tg genotype do not express any MITFs. It was previously reported that mi/mi CMCs showed more severe abnormalities than tg/tg CMCs, indicating that mi-MITF had inhibitory function. Whereas mi-MITF contains a single amino acid deletion in the basic domain, MITF encoded by mi(ew) allele (ew-MITE) deletes 16 of 21 amino acids of the basic domain. Here the effect of a large deletion of the basic domain was examined. In mi(ew)/mi(ew) CMCs, the expression pattern of genes whose transcription was affected by MITF was comparable to that of tg/tg CMCs rather than to that of mi/mi CMCs. This suggested that ew-MITF lacked any functions. The part of the basic domain deleted in ew-MITF appeared necessary for either transactivation or inhibition of transactivation. (Blood. 2001;98:2577-2579) (C) 2001 by The American Society of Hematology.
引用
收藏
页码:2577 / 2579
页数:3
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