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Signal transducer and activator of transcription (STAT)-3 regulates microRNA gene expression in chronic lymphocytic leukemia cells

机译:信号转导子和转录激活子(STAT)-3调节慢性淋巴细胞白血病细胞中的microRNA基因表达

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摘要

Backgrounds Approximately 1,000 microRNAs (miRs) are present in the human genome; however, little is known about the regulation of miR transcription. Because miR levels are deregulated in chronic lymphocytic leukemia (CLL) and signal transducer and activator of transcription ( STAT )-3 is constitutively activated in CLL, we sought to determine whether STAT3 affects the transcription of miR genes in CLL cells. Methods We used publically available data from the ENCODE project to identify putative STAT3 binding sites in the promoters of miR genes. Then we transfected CLL cells with STAT3 -shRNA or with an empty vector, and to determine which miRs are differentially expressed, we used a miR microarray approach followed by validation of the microarray results for 6 miRs using quantitative real-time polymerase chain reaction (qRT-PCR). Results We identified putative STAT3 binding sites in 160 promoter regions of 200 miRs, including miR-21, miR-29, and miR-155, whose levels have been reported to be upregulated in CLL. Levels of 72 miRs were downregulated (n = 63) or upregulated (n = 9). qRT-PCR confirmed the array data in 5 of 6 miRs. Conclusions The presence of activated STAT3 has a profound effect on miR expression in CLL cells.
机译:背景技术人类基因组中存在大约1,000个microRNA(miR);然而,关于miR转录的调控知之甚少。由于miR水平在慢性淋巴细胞性白血病(CLL)中被解除调节,并且在CLL中组成性地激活了信号转导和转录激活因子(STAT)-3,因此我们试图确定STAT3是否影响CLL细胞中miR基因的转录。方法我们使用了来自ENCODE项目的公开数据,以鉴定miR基因启动子中假定的STAT3结合位点。然后,我们用STAT3 -shRNA或空载体转染CLL细胞,并确定差异表达的miR,我们使用miR微阵列方法,然后使用定量实时聚合酶链反应(qRT)验证了6 miR的微阵列结果-PCR)。结果我们在200个miR的160个启动子区域(包括miR-21,miR-29和miR-155)中确定了推测的STAT3结合位点,据报道其水平在CLL中被上调。 72个miR的水平下调(n = 63)或上调(n = 9)。 qRT-PCR在6个miR中的5个中确认了阵列数据。结论激活的STAT3的存在对CLL细胞中miR表达有深远的影响。

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