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第1外显子中的GATA-1结合位点指导PPOX的红系特异性转录。

GATA-1 binding sites in exon 1 direct erythroid-specific transcription of PPOX.

作者信息

de Vooght Karen M K, van Wijk Richard, van Solinge Wouter W

机构信息

Department of Clinical Chemistry and Haematology, University Medical Center Utrecht, Utrecht, The Netherlands.

出版信息

Gene. 2008 Feb 15;409(1-2):83-91. doi: 10.1016/j.gene.2007.11.010. Epub 2007 Dec 4.

Abstract

We investigated erythroid-specific expression of the human PPOX gene. This gene encodes protoporphyrinogen oxidase, which is involved in synthesizing heme for red blood cells and heme as a cofactor for the respiratory cytochromes. In vitro luciferase transfection assays in human uninduced and hemin induced erythroleukemic K562 cells showed that the presence of exon 1 increased promoter activity fourfold as compared to reporter constructs lacking this exon. This transcriptional regulation was mediated by two GATA-1 sites in exon 1. Electrophoretic mobility shift and chromatin immunoprecipitation assays demonstrated that both GATA sites were able to bind GATA-1 in vitro and in vivo. Exon 1 did not affect promoter activity in human hepatoma HepG2 cells and U937 monocytic cells but its presence decreased promoter activity in HeLa human cervical carcinoma cells. We conclude that the GATA-1 binding sites in exon 1 constitute key regulatory elements in differential expression of PPOX in erythroid and non-erythroid cells.

摘要

我们研究了人类PPOX基因的红系特异性表达。该基因编码原卟啉原氧化酶,其参与为红细胞合成血红素以及作为呼吸细胞色素的辅因子的血红素合成。在人未诱导和血红素诱导的红白血病K562细胞中的体外荧光素酶转染试验表明,与缺乏该外显子的报告构建体相比,外显子1的存在使启动子活性增加了四倍。这种转录调控由外显子1中的两个GATA-1位点介导。电泳迁移率变动分析和染色质免疫沉淀试验表明,这两个GATA位点在体外和体内均能够结合GATA-1。外显子1对人肝癌HepG2细胞和U937单核细胞的启动子活性没有影响,但其存在会降低人宫颈癌HeLa细胞中的启动子活性。我们得出结论,外显子1中的GATA-1结合位点构成了PPOX在红系和非红系细胞中差异表达的关键调控元件。

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