| Literature DB >> 18776907 |
Sawako Muroi1, Yoshinori Naoe, Chizuko Miyamoto, Kaori Akiyama, Tomokatsu Ikawa, Kyoko Masuda, Hiroshi Kawamoto, Ichiro Taniuchi.
Abstract
CD4 and the transcription factor ThPOK are essential for the differentiation of major histocompatibility complex class II-restricted thymocytes into the helper T cell lineage; their genes (Cd4 and Zbtb7b (called 'ThPOK' here)) are repressed by transcriptional silencer elements in cytotoxic T cells. The molecular mechanisms regulating expression of these genes during helper T cell lineage differentiation remain unknown. Here we showed that inefficient upregulation of ThPOK, induced by removal of the proximal enhancer from the ThPOK locus, resulted in the transdifferentiation of helper lineage-specified cells into the cytotoxic T cell lineage. Furthermore, direct antagonism by ThPOK of the Cd4 and ThPOK silencers generated two regulatory loops that initially inhibited Cd4 downregulation and later stabilized ThPOK expression. Our results show how an initial lineage-specification signal can be amplified and stabilized during the lineage-commitment process.Entities:
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Year: 2008 PMID: 18776907 DOI: 10.1038/ni.1650
Source DB: PubMed Journal: Nat Immunol ISSN: 1529-2908 Impact factor: 25.606