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Domain analyses of the Runx1 transcription factor responsible for modulating T‐cell receptor‐β/CD4 and interleukin‐4/interferon‐γ expression in CD4 + peripheral T lymphocytes
Author(s) -
Uchino Ryuji
Publication year - 2009
Publication title -
immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.297
H-Index - 133
eISSN - 1365-2567
pISSN - 0019-2805
DOI - 10.1111/j.1365-2567.2009.03042.x
Subject(s) - runx1 , transcription factor , biology , gene expression , microbiology and biotechnology , t cell , interleukin 2 , irf8 , interleukin 4 , regulation of gene expression , stat4 , receptor , signal transduction , gene , immune system , immunology , genetics , stat , stat3
Summary The Runx1 transcription factor is one of the master regulators of T‐lymphocyte differentiation. There have been several reports trying to assign a domain within the Runx1 protein that is responsible for gene expression in thymocytes. The Runx1 domains involved in regulating the expression of several genes in peripheral CD4 + T cells were analysed. It was observed that Runx1 over‐expression enhanced the surface expression of CD4 and CD69 molecules via its activation domain and VWRPY domain, and decreased that of T‐cell receptor‐β via its activation domain. Runx1 over‐expression enhanced interferon‐γ expression via its activation and VWRPY domains, and abolished interleukin‐4 expression through its activation domain. Transduction of Runx1 did not down‐regulate CD4 expression until 72 hr of culture, but the repression of CD4 expression became evident after 96 hr. The main region responsible for repressing CD4 expression was the inhibitory domain of Runx1. Taken together, these results lead to a proposal that the regions in Runx1 responsible for modulating gene expression are distinct in thymocytes and in peripheral CD4 + T cells.