The IL-7 receptor (IL-7R) controls the accessibility of mouse TCR gamma locus, by recruiting STAT5 and transcriptional coactivators to the J gamma 1 germline promoter and inducing histone acetylation at nearby chromatin. Although a STAT motif is present in J gamma 4 germline promoter, it is still unknown whether STAT5 regulates the transcription of the J gamma 4 promoter. Here, we showed that cytokine stimulation induced J gamma 4-C gamma 4 germline transcripts in a pre-T cell line, Scid.adh, and a hematopoietic cell line, Ba/F3. A STAT consensus motif was present in 5' region of J gamma 4 gene segment. We found that STAT5 bound to the STAT motif of the J gamma 4 germline promoter in vitro by EMSA. In addition, we detected by chromatin immunoprecipitation assay that STAT5 was recruited to the endogenous J gamma 4 chromatin in Ba/F3 cells after cytokine stimulation. Finally, using reporter assay, we showed that the J gamma 4 germline promoter was activated by STAT5 and that mutation in the STAT motif abrogated the activity. Furthermore, this transactivation was augmented by transcriptional coactivators, CBP and p300. Collectively, these results demonstrate that STAT5 binds to the STAT motif in the J gamma 4 promoter and induces germline transcription. Thus, this study indicates that the IL-7R/STAT5 signal controls the transcription and accessibility of different clusters in the TCR gamma locus. (c) 2007 Elsevier Ltd. All rights reserved.