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髓过氧化物酶基因第7和第9内含子中转录顺式元件的鉴定

Identification of transcriptional cis-elements in introns 7 and 9 of the myeloperoxidase gene.

作者信息

Yamada M, Yoshida M, Hashinaka K

机构信息

Institute for Protein Research, Osaka University, Japan.

出版信息

J Biol Chem. 1993 Jun 25;268(18):13479-85.

PMID:8390465
Abstract

We studied the transcriptional cis-acting elements of the myeloperoxidase gene, which is expressed during the promyelocyte stage of granulocyte development by assay of transient expression of the chloramphenicol acetyltransferase (CAT) gene in myeloid leukemia SKM-1 cells and analysis of the DNA binding sites for HL-60 nuclear factors. Assay of CAT expression dependent on restriction fragments isolated from genomic clones indicated that the fragments located on introns 7 and 9 enhanced the expression. Methylation interference experiments showed that the guanine residues in a consensus sequence of an estrogen response element in the intron 7 fragment interacted with a nuclear factor. Gel retardation analysis indicated that this interaction of the intron 7 fragment with the nuclear factor was specifically inhibited by an oligodeoxynucleotide containing the 21-base pair (bp) estrogen response element. DNase I footprint analysis revealed that a 36-bp-specific sequence of the intron 9 fragment was protected from DNase I by nuclear extracts. This sequence contained a palindromic sequence consisting of the conserved half-motif of an estrogen response element with 5-bp spacing. The interaction of the intron 9 fragment with the nuclear extracts was specifically inhibited by an oligodeoxynucleotide of the 36-bp sequence. Furthermore, the 21- and 36-bp oligodeoxynucleotides in the constructs enhanced CAT expression in the cells. These results suggest that these elements in introns 7 and 9 are involved in expression of the myeloperoxidase gene.

摘要

我们通过在髓系白血病SKM-1细胞中检测氯霉素乙酰转移酶(CAT)基因的瞬时表达以及分析HL-60核因子的DNA结合位点,研究了髓过氧化物酶基因的转录顺式作用元件,该基因在粒细胞发育的早幼粒细胞阶段表达。对依赖于从基因组克隆中分离的限制性片段的CAT表达进行检测表明,位于内含子7和9上的片段增强了表达。甲基化干扰实验表明,内含子7片段中雌激素反应元件共有序列中的鸟嘌呤残基与一种核因子相互作用。凝胶阻滞分析表明,内含子7片段与核因子的这种相互作用被含有21个碱基对(bp)雌激素反应元件的寡脱氧核苷酸特异性抑制。DNase I足迹分析显示,内含子9片段的一个36-bp特异性序列被核提取物保护而免受DNase I的作用。该序列包含一个回文序列,由具有5-bp间隔的雌激素反应元件保守半基序组成。内含子9片段与核提取物的相互作用被36-bp序列的寡脱氧核苷酸特异性抑制。此外,构建体中的21-bp和36-bp寡脱氧核苷酸增强了细胞中的CAT表达。这些结果表明,内含子7和9中的这些元件参与了髓过氧化物酶基因的表达。

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