AbstractChanges in chromatin structure underlie the activation or silencing of genes during development. The chromatin remodeler Mi-2β is highly expressed in thymocytes and is presumed to be a transcriptional repressor because of its presence in the nucleosome remodeling deacetylase (NuRD) complex. Using conditional inactivation, we show that Mi-2β is required at several steps during T cell development: for differentiation of β selected immature thymocytes, for developmental expression of CD4, and for cell divisions in mature T cells. We further show that Mi-2β plays a direct role in promoting CD4 gene expression. Mi-2β associates with the CD4 enhancer as well as the E box binding protein HEB and the histone acetyltransferase (HAT) p300, en...
During development, progenitor cells with binary potential give rise to daughter cells that have dis...
T cells coordinate immune functions by differentiating into highly specialised cellular lineages tha...
AbstractGATA-3 is expressed at higher levels in CD4 than in CD8 SP thymocytes. Here we show that upr...
AbstractChanges in chromatin structure underlie the activation or silencing of genes during developm...
AbstractCD4 and CD8 genes are integral indicators of T-cell lineage commitment. New insights into th...
SummaryLineage commitment is induced by changes in gene expression dictated by the intimate interact...
AbstractDifferentiating cells undergo programmed alterations in their patterns of gene expression, w...
During an immune response, a naive CD4+ helper T cell undergoes a program of proliferation and diffe...
T-cells retain cell-type-specific programming for IL-2 inducibility through many rounds of division ...
Dynamic changes in chromatin structure through ATP-dependent remodeling and covalent modifications o...
Mammalian SWI–SNF-related complexes use brahma-related gene 1 (Brg1) as a catalytic subunit to remod...
SummaryT lymphocytes differentiate in discrete stages within the thymus. Immature thymocytes lacking...
Mammalian SWI-SNF-related complexes use brahma-related gene 1 (Brg1) as a catalytic subunit to remod...
We analyzed the activity of the enhancer, the promoter and the silencer of the human CD4 gene during...
AbstractWe recently identified a 3′ region of the rad50 gene possessing strong enhancer activity as ...
During development, progenitor cells with binary potential give rise to daughter cells that have dis...
T cells coordinate immune functions by differentiating into highly specialised cellular lineages tha...
AbstractGATA-3 is expressed at higher levels in CD4 than in CD8 SP thymocytes. Here we show that upr...
AbstractChanges in chromatin structure underlie the activation or silencing of genes during developm...
AbstractCD4 and CD8 genes are integral indicators of T-cell lineage commitment. New insights into th...
SummaryLineage commitment is induced by changes in gene expression dictated by the intimate interact...
AbstractDifferentiating cells undergo programmed alterations in their patterns of gene expression, w...
During an immune response, a naive CD4+ helper T cell undergoes a program of proliferation and diffe...
T-cells retain cell-type-specific programming for IL-2 inducibility through many rounds of division ...
Dynamic changes in chromatin structure through ATP-dependent remodeling and covalent modifications o...
Mammalian SWI–SNF-related complexes use brahma-related gene 1 (Brg1) as a catalytic subunit to remod...
SummaryT lymphocytes differentiate in discrete stages within the thymus. Immature thymocytes lacking...
Mammalian SWI-SNF-related complexes use brahma-related gene 1 (Brg1) as a catalytic subunit to remod...
We analyzed the activity of the enhancer, the promoter and the silencer of the human CD4 gene during...
AbstractWe recently identified a 3′ region of the rad50 gene possessing strong enhancer activity as ...
During development, progenitor cells with binary potential give rise to daughter cells that have dis...
T cells coordinate immune functions by differentiating into highly specialised cellular lineages tha...
AbstractGATA-3 is expressed at higher levels in CD4 than in CD8 SP thymocytes. Here we show that upr...