Deficient transcription of mouse mast cell protease 4 gene in mutant mice of mi/mi genotype

被引:45
作者
Jippo, T
Lee, YM
Katsu, Y
Tsujino, K
Morii, E
Kim, DK
Kim, HM
Kitamura, Y
机构
[1] Osaka Univ, Sch Med, Dept Pathol, Suita, Osaka 5650871, Japan
[2] Wonkwang Univ, Coll Pharm, Dept Oriental Pharm, Chonbuk, South Korea
关键词
D O I
10.1182/blood.V93.6.1942.406k08_1942_1950
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The mi locus encodes a member of the basic-helix-loop-helix-leucine zipper (bHLH-Zip) protein family of transcription factors thereafter called MITF). We reported that expression of the mouse mast cell protease 5 (MMCP-5) and MMCP-6 genes were deficient in cultured mast cells (CMC) derived from mutant mice of mi/mi genotype. Despite the reduced expression of both MMCP-5 and MMCP-6, their regulation mechanisms were different. Because MMCP-5 is a chymase and MMCP-6 a tryptase, there was a possibility that the difference in regulation mechanisms was associated with their different characteristics as proteases. We compared the regulation mechanisms of another chymase, MMCP-4 with those of MMCP-5 and MMCP-6. The expression of the MMCP-4 gene was also deficient in mi/mi CMC. The overexpression of the normal (+) MITF but not of mi-MITF normalized the poor expression of the MMCP-4 gene in mi/mi CMC, indicating the involvement of +-MITF in transactivation of the MMCP-4 gene. Although MMCP-4 is chymase as MMCP-5, the regulation of MMCP-4 expression was more similar to MMCP-6 than to MMCP-5. We also showed the deficient expression of granzyme B and cathepsin G genes in mi/mi CMC. Genes encoding granzyme B, cathepsin G, MMCP-4 and MMCP-5 are located on chromosome 14. Because all these genes showed deficient expression in mi/mi CMC, there is a possibility that MITF might regulate the expression of these genes through a locus control region. (C) 1999 by The American Society of Hematology.
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页码:1942 / 1950
页数:9
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