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Regulation of mouse Scgb3a1 gene expression by NF-Y and association of CpG methylation with its tissue-specific expression

机译:NF-Y对小鼠Scgb3a1基因表达的调控以及CpG甲基化与其组织特异性表达的关联

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Background:Secretoglobin(SCGB)3A1 is a secretory protein of small molecular weight with tumor suppressor function.It is highly expressed in lung and trachea in both human and mouse, with additional tissues expressing the protein that differ depending on the species.However,little is known about the function and transcriptional regulation of this gene in normal mouse tissues. Results:By reporter gene transfection and gel mobility shift analyses,we demonstrated that expression of the mouse Scgb3a1 gene is regulated by a PU-box binding protein and a ubiquitous transcription factor NF-Y that respectively binds to the PU-boxes located at-99 to-105 bp and- 158 to-164 bp,and the"CCAAT"binding sites located at-425 to-429 bp and-498 to-502 bp from the transcription start site of the gene.However,the effect of PU-box binding protein on transcriptional activation is minimal as compared to NF-Y,suggesting that NF-Y is a more critical transcription factor for mouse Scgb3a1 gene transcription.Despite that NF-Y is a ubiquitous factor, Scgb3a1 is highly expressed only in mouse lung and mtCC cells that are derived from SV40 transformed mouse Clara cells,but not in ten other mouse tissues/cells examined.Gene methylation analysis revealed that within 600 bp of the Scgb3a1 gene promoter region,there are nine CpG methylation sites present,of which two CpGs closest to the transcription start site of the gene are unmethylated in the tissues/cells expressing SCGB3A1. Conclusion:A ubiquitous transcription factor NF-Y binds to and activates expression of the mouse Scgb3a1 gene and tissue-specific expression of the gene is associated with CpG methylation of the promoter.
机译:背景:血红蛋白(SCGB)3A1是一种具有抑癌功能的小分子量分泌蛋白,在人和小鼠的肺和气管中高表达,另外的组织表达的蛋白因物种而异。已知该基因在正常小鼠组织中的功能和转录调控。结果:通过报告基因转染和凝胶迁移率迁移分析,我们证明了小鼠Scgb3a1基因的表达受PU-box结合蛋白和泛在转录因子NF-Y的调控,后者分别与位于-99处的PU-boxs结合到-105bp至-158bp至-164bp,和“ CCAAT”结合位点位于距基因转录起始位点-425--429bp和-498-502bp之间。然而,PU-的作用框结合蛋白对转录激活的影响比NF-Y最小,这表明NF-Y是小鼠Scgb3a1基因转录的一个更关键的转录因子。尽管NF-Y是一种普遍存在的因子,但Scgb3a1仅在小鼠肺中高表达以及从SV40转化的小鼠Clara细胞衍生的mtCC和mtCC细胞,但未在其他十个小鼠组织/细胞中检测到。基因甲基化分析显示,在Scgb3a1基因启动子区域的600 bp之内,存在9个CpG甲基化位点,其中两个最接近反式的CpG在表达SCGB3A1的组织/细胞中,该基因的爬行起始位点未甲基化。结论:无处不在的转录因子NF-Y结合并激活小鼠Scgb3a1基因的表达,该基因的组织特异性表达与启动子的CpG甲基化有关。

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