
CD4 cells from mice heterozygous for an IL-4 and a GFP/IL-4 gene frequently express a single allele. Analysis of IL-4 or GFP production by cells from recently primed Th2 cells indicates that essentially all are competent to transcribe either allele but have a low probability of doing so. By contrast, long-term Th2 clones show distinct and heritable ratios in the proportion of cells that express IL-4 or GFP. We conclude that in the course of Th2 priming an early efficient event renders both alleles capable of being inefficiently transcribed; a second, less frequent event occurs that renders one allele more competent, accounting for the differential expression of IL-4 and GFP in different clones.
CD4-Positive T-Lymphocytes, Male, Green Fluorescent Proteins, GATA3 Transcription Factor, DNA-Binding Proteins, Mice, Inbred C57BL, Luminescent Proteins, Mice, Th2 Cells, Gene Expression Regulation, Trans-Activators, Animals, Female, Interleukin-4, RNA, Messenger, Alleles, Cells, Cultured
CD4-Positive T-Lymphocytes, Male, Green Fluorescent Proteins, GATA3 Transcription Factor, DNA-Binding Proteins, Mice, Inbred C57BL, Luminescent Proteins, Mice, Th2 Cells, Gene Expression Regulation, Trans-Activators, Animals, Female, Interleukin-4, RNA, Messenger, Alleles, Cells, Cultured
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