Masui Naomi, Tani-ichi Shizue, Maki Kazushige, Ikuta Koichi
Laboratory of Biological Protection, Department of Biological Responses, Institute for Virus Research, Kyoto University, 53 Shogoin-Kawahara-cho, Sakyo-ku, Kyoto 606-8507, Japan.
Mol Immunol. 2008 Feb;45(3):849-55. doi: 10.1016/j.molimm.2007.06.157. Epub 2007 Jul 30.
The IL-7 receptor (IL-7R) controls the accessibility of mouse TCRgamma locus, by recruiting STAT5 and transcriptional coactivators to the Jgamma1 germline promoter and inducing histone acetylation at nearby chromatin. Although a STAT motif is present in Jgamma4 germline promoter, it is still unknown whether STAT5 regulates the transcription of the Jgamma4 promoter. Here, we showed that cytokine stimulation induced Jgamma4-Cgamma4 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 Jgamma4 gene segment. We found that STAT5 bound to the STAT motif of the Jgamma4 germline promoter in vitro by EMSA. In addition, we detected by chromatin immunoprecipitation assay that STAT5 was recruited to the endogenous Jgamma4 chromatin in Ba/F3 cells after cytokine stimulation. Finally, using reporter assay, we showed that the Jgamma4 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 Jgamma4 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 TCRgamma locus.
白细胞介素-7受体(IL-7R)通过将信号转导子和转录激活子5(STAT5)及转录共激活因子募集至Jgamma1种系启动子,并诱导附近染色质的组蛋白乙酰化,来控制小鼠T细胞受体γ链(TCRgamma)基因座的可及性。尽管在Jgamma4种系启动子中存在一个STAT基序,但STAT5是否调节Jgamma4启动子的转录仍不清楚。在此,我们表明细胞因子刺激可在一个前T细胞系Scid.adh和一个造血细胞系Ba/F3中诱导Jgamma4-Cgamma4种系转录本。在Jgamma4基因片段的5'区域存在一个STAT共有基序。我们通过电泳迁移率变动分析(EMSA)发现STAT5在体外与Jgamma4种系启动子的STAT基序结合。此外,我们通过染色质免疫沉淀分析检测到,细胞因子刺激后,STAT5被募集至Ba/F3细胞中的内源性Jgamma4染色质。最后,利用报告基因分析,我们表明Jgamma4种系启动子被STAT5激活,且STAT基序中的突变消除了该活性。此外,这种反式激活被转录共激活因子CBP和p300增强。总体而言,这些结果表明STAT5与Jgamma4启动子中的STAT基序结合并诱导种系转录。因此,本研究表明IL-7R/STAT5信号控制TCRgamma基因座中不同簇的转录和可及性。