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CIS是一种细胞因子诱导的SH2蛋白,是JAK-STAT5信号通路的靶点,并调节STAT5的激活。

CIS, a cytokine inducible SH2 protein, is a target of the JAK-STAT5 pathway and modulates STAT5 activation.

作者信息

Matsumoto A, Masuhara M, Mitsui K, Yokouchi M, Ohtsubo M, Misawa H, Miyajima A, Yoshimura A

机构信息

Insititute of Life Science, Kurume University, Japan.

出版信息

Blood. 1997 May 1;89(9):3148-54.

PMID:9129017
Abstract

We searched for immediate early cytokine responsive genes and isolated a novel gene, CIS (Cytokine Inducible SH2 containing protein) that is induced in hematopoietic cells by a subset of cytokines including interleukin-2 (IL-2), IL-3, and erythropoietin (EPO). The mutant IL-2 receptor that fails to activate STAT5 could not induce CIS, suggesting that STAT5 is involved in the cytokine-inducible expression of CIS. We cloned the 5'-flanking region of the CIS gene and found that about 200 bases upstream of the transcription-initiation site contain four potential STAT5 binding sites (MGF boxes). Luciferase reporter assays showed that these MGF boxes were essential for EPO-dependent promoter activity. Expression of STAT5 and the EPO receptor in HEK293 cells conferred EPO-dependent activation of the CIS promoter. These data indicate that CIS is a target of the JAK-STAT5 pathway of cytokine receptors. CIS contains an SH2 domain and binds to tyrosine-phosphorylated EPO and IL-3 receptors. In HEK293 cells expressing STAT5 and the EPO receptor, EPO-dependent tyrosine phosphorylation of STAT5, as well as EPO-dependent CIS-promoter activation, was suppressed when CIS was coexpressed. Moreover, the induction of oncostatin M, another STAT5 target, as well as the tyrosine-phosphorylation of STAT5, were partially suppressed by CIS expression in Ba/F3 cells. Thus, CIS is a feedback modulator of STAT5; its expression is induced by STAT5 and it negatively modulates STAT5 activation.

摘要

我们搜索了即时早期细胞因子反应基因,并分离出一个新基因CIS(含细胞因子诱导性SH2结构域蛋白),该基因在造血细胞中可被包括白细胞介素-2(IL-2)、IL-3和促红细胞生成素(EPO)在内的一部分细胞因子诱导表达。无法激活STAT5的突变型IL-2受体不能诱导CIS表达,这表明STAT5参与了CIS的细胞因子诱导性表达。我们克隆了CIS基因的5'侧翼区,发现转录起始位点上游约200个碱基包含四个潜在的STAT5结合位点(MGF框)。荧光素酶报告基因检测表明,这些MGF框对于EPO依赖的启动子活性至关重要。在HEK293细胞中表达STAT5和EPO受体可使CIS启动子发生EPO依赖的激活。这些数据表明CIS是细胞因子受体JAK-STAT5信号通路的一个靶点。CIS含有一个SH2结构域,可与酪氨酸磷酸化的EPO受体和IL-3受体结合。在表达STAT5和EPO受体的HEK293细胞中,共表达CIS时,STAT5的EPO依赖的酪氨酸磷酸化以及EPO依赖的CIS启动子激活均受到抑制。此外,在Ba/F3细胞中,CIS的表达可部分抑制另一个STAT5靶点抑瘤素M的诱导以及STAT5的酪氨酸磷酸化。因此,CIS是STAT5的一个反馈调节因子;其表达由STAT5诱导,并且对STAT5的激活起负调节作用。

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