We have used various mouse mutants for studying the development of mast cel
ls. The bone marrow origin of mast cells was shown by using giant granules
of beige mice as a marker. Mast cell-deficient W/W-v and Sl/Sl(d) mice are
useful far investigation of the developmental processes. The mi locus encod
es a member of the basic helix-loop-helix-leucine zipper protein family of
transcription factors (MITF), and mast cells of mi/mi mice showed phenotypi
c abnormalities. Mast cells of mi/mi mice synthesized the mutant mi-MITF in
normal amounts, and mi-MITF showed an inhibitory effect on the transcripti
on of various mast cell-specific genes. On the other hand, mice of tg/tg po
ssess the transgene insertional mutation in the 5' flanking region of the m
i gene and do not express any MITFs. Genes whose transcription was suppress
ed were more numerous in mast cells of mi/mi mice than in those of tg/tg mi
ce. The comparison between phenotypes of mi/mi mast cells and those of tg/t
g mast cells gave some insights into the regulation of mast cell phenotypes
by transcription factors. Copyright (C) 2001 S. Karger AG,Basel.