Abstract
GATA-3 is a master regulator of T helper type 2 (T(H)2) differentiation. However, the molecular basis of GATA-3-mediated T(H)2 lineage commitment is poorly understood. Here we identify the DNase I-hypersensitive site 2 (HS2) element located in the second intron of the interleukin 4 locus (Il4) as a critical enhancer strictly controlled by GATA-3 binding. Mice lacking HS2 showed substantial impairment in their asthmatic responses and their production of IL-4 but not of other T(H)2 cytokines. Overexpression of Gata3 in HS2-deficient T cells failed to restore Il4 expression. HS2 deletion impaired the trimethylation of histone H3 at Lys4 and acetylation of histone H3 at Lys9 and Lys14 in the Il4 locus. Our results indicate that HS2 is the target of GATA-3 in regulating chromosomal modification of the Il4 locus and is independent of the Il5 and Il13 loci.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Asthma / chemically induced
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Asthma / genetics
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Asthma / immunology
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Asthma / metabolism*
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Cell Differentiation
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Cell Lineage
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Cells, Cultured
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DNA Methylation / genetics
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DNA Methylation / immunology
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Deoxyribonuclease I / genetics
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Deoxyribonuclease I / metabolism
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Enhancer Elements, Genetic / genetics
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GATA3 Transcription Factor / genetics
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GATA3 Transcription Factor / immunology
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GATA3 Transcription Factor / metabolism*
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Gene Expression Regulation / immunology
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Histones / metabolism*
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Inteins / genetics
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Interleukin-4 / genetics
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Interleukin-4 / immunology
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Interleukin-4 / metabolism*
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Mice
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Mice, Inbred C57BL
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Mice, Knockout
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Protein Binding / genetics
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Sequence Deletion / genetics
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Th2 Cells / immunology
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Th2 Cells / metabolism*
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Th2 Cells / pathology
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Transgenes / genetics
Substances
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GATA3 Transcription Factor
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Histones
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Interleukin-4
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Deoxyribonuclease I