Publication | Open Access
EZH2 and Histone 3 Trimethyl Lysine 27 Associated with Il4 and Il13 Gene Silencing in TH1 Cells
151
Citations
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References
2005
Year
Histone ModificationsEpigenetic ChangeT-regulatory CellImmunologyIl13 Gene SilencingCd4 T Cell ResponsesImmunotherapyEpigeneticsImmune DysregulationT Helper 1ImmunogeneticsLysine 27Cell SignalingAutoimmune DiseaseAllergyHistone 3Canonical TAutoimmunityCell BiologyChromatin FunctionChromatinCytokineChromatin StructureImmune Cell DevelopmentNatural SciencesEpigenomicsTrimethyl Lysine 27Medicine
Differentiation of naïve CD4 T cells toward the T helper 1 (T(H)1) and T helper 2 (T(H)2) fates involves the transcriptional repression and enhancement, respectively, of Il4 and Il13, adjacent chromosome 11 genes encoding the canonical T(H)2 cytokines interleukin-4 and interleukin-13. Proper execution of this developmental fate choice during immune responses is critical to host defense and, when misregulated, leads to susceptibility to infectious microbes and to allergic and autoimmune diseases. Here, using chromatin immunoprecipitation and real time reverse transcription PCR we identify the Polycomb family histone methyltransferase EZH2 as the enzyme responsible for methylating lysine 27 of histone H3 at the Il4-Il13 locus of T(H)1 but not T(H)2 cells, implicating EZH2 in the mechanism of Il4 and Il13 transcriptional silencing.
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