首页> 美国卫生研究院文献>Nucleic Acids Research >Identification of an intronic enhancer that nullifies upstream repression of SPARC gene expression.
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Identification of an intronic enhancer that nullifies upstream repression of SPARC gene expression.

机译:鉴定使SPARC基因表达的上游阻遏无效的内含子增强子。

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摘要

The SPARC gene 5'flanking sequence has been shown to contain enhancer elements, but also negative control elements immediately upstream of the enhancer elements. Although these 5'enhancer elements are active in F9 and PYS-2 cells, their activities are nullified by the 5'repressor activity. In the present study we have identified within intron 1 between nucleotides (nt) +5000 and +5150 of the SPARC gene an enhancer element that bound to two transcription factors of 48 and 52 kDa and between nt +5000 and +5523 a DNase I hypersensitive site. Furthermore, a region containing the 3'intron 1 enhancer element, together with the 5'enhancer elements, neutralized the 5'repressor activity and stimulated efficient transcription. The resulting SPARC promoter activity is about equal in F9, differentiated F9 and PYS-2 cells. We consistently found that the rate of SPARC transcription is nearly the same in F9 and PYS-2 cells. Association of the 3'enhancer element in intron 1 with the DNase I hypersensitive site suggests that both play a role in regulating SPARC expression in vivo .
机译:已经显示出SPARC基因的5'侧翼序列含有增强子元件,但是还包含紧邻增强子元件上游的阴性对照元件。尽管这些5'增强子元件在F9和PYS-2细胞中具有活性,但其活性却被5'阻遏物活性所抵消。在本研究中,我们已经在内含子1中鉴定了SPARC基因的核苷酸(nt)+5000和+5150之间的增强子元件,该元件与两个转录因子48和52 kDa结合,并且在nt +5000和+5523之间有DNase I过敏现场。此外,含有3'内含子1增强子元件和5'增强子元件的区域中和了5'阻遏物活性并刺激了有效的转录。最终的SPARC启动子活性在F9,分化的F9和PYS-2细胞中大约相等。我们始终发现,F9和PYS-2细胞中SPARC转录的速率几乎相同。内含子1中3'增强子元件与DNase I超敏位点的关联表明两者都在体内调节SPARC表达中发挥作用。

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