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Expression regulation of AP-2 gamma gene.

机译:AP-2γ基因的表达调控。

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摘要

AP-2gamma is a member of the AP-2 transcription factor family, is highly enriched in the trophoblast cell lineage, and is essential for placenta development. In an effort to identify factors regulating AP-2gamma gene expression we isolated and characterized the promoter and 5' flanking region of the mouse and human AP-2gamma genes. The transcription start site of the mouse AP-2gamma gene was mapped by primer extension and 5' RACE. Transient gene transfer studies showed that basal promoter activity resides within a highly conserved ∼200 by DNA sequence located immediately upstream of the transcription start site. The conserved region is highly GC-rich and lacks typical TATA or CCAAT boxes. Multiple potential Sp and AP-2 binding sites are clustered within this region. Electrophoretic mobility shift assays demonstrated that Sp1 and Sp3 bind to three sites in the promoter region of the mouse AP-2gamma gene. Combined mutation of the three putative Sp sites reduced promoter activity by 80% in trophoblast and non-trophoblast cells, demonstrating the functional importance of these sites in AP-2gamma gene expression.; Mutational analysis of the 5'-flanking region revealed a 117-bp positive regulatory region of the mouse AP-2gamma gene located between -5700 and -5583 upstream of the transcription start site. This 117-bp positive regulatory element provided approximately 7-fold enhancement of reporter gene expression in cultured trophoblast cells. A C/EBP-Sp1 transcription factor-binding module is located in this DNA sequence. Electrophoretic mobility shift assays demonstrated that transcription factors Sp1, Sp3 and C/EBP bind to the enhancer element. Mutation of each protein-binding site reduced the enhanced expression significantly. Mutagenesis assays showed that two other protein-binding sites also contribute to the enhancer activity. In summary, we have shown that Sp1 and Sp3 bind to cis-regulatory elements located in the promoter region and contribute to basal promoter activity. We have identified a 117-bp positive regulatory element of AP-2gamma gene, and we have shown that Sp and C/EBP proteins bind to the cis -regulatory elements and contribute to the enhanced gene expression.
机译:AP-2gamma是AP-2转录因子家族的成员,在滋养层细胞谱系中高度富集,对胎盘发育至关重要。为了确定调节AP-2gamma基因表达的因素,我们分离并鉴定了小鼠和人AP-2gamma基因的启动子和5'侧翼区域。通过引物延伸和5'RACE定位小鼠AP-2gamma基因的转录起始位点。瞬时基因转移研究表明,基础启动子活性位于紧邻转录起始位点上游的DNA序列高度保守的〜200个范围内。该保守区富含GC,并且没有典型的TATA或CCAAT盒。多个潜在的Sp和AP-2结合位点聚集在该区域内。电泳迁移率迁移分析表明,Sp1和Sp3与小鼠AP-2gamma基因启动子区域的三个位点结合。三个推定的Sp位点的组合突变在滋养层细胞和非滋养层细胞中使启动子活性降低了80%,证明了这些位点在AP-2γ基因表达中的功能重要性。对5'侧翼区域的突变分析显示,小鼠AP-2gamma基因的117 bp正调控区位于转录起始位点上游-5700和-5583之间。该117bp的阳性调控元件在培养的滋养细胞中提供了约7倍的报告基因表达增强。 C / EBP-Sp1转录因子结合模块位于此DNA序列中。电泳迁移率变动分析表明,转录因子Sp1,Sp3和C / EBP与增强子结合。每个蛋白质结合位点的突变显着降低了增强的表达。诱变分析表明,另外两个蛋白质结合位点也有助于增强子的活性。总之,我们已经显示Sp1和Sp3与位于启动子区域的顺式调节元件结合,并有助于基础启动子活性。我们已经确定了AP-2gamma基因的117 bp阳性调控元件,并且我们已经显示Sp和C / EBP蛋白与顺式调控元件结合并有助于增强基因表达。

著录项

  • 作者

    Li, Mei.;

  • 作者单位

    The University of Texas Graduate School of Biomedical Sciences at Houston.;

  • 授予单位 The University of Texas Graduate School of Biomedical Sciences at Houston.;
  • 学科 Biology Molecular.
  • 学位 Ph.D.
  • 年度 2005
  • 页码 148 p.
  • 总页数 148
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 分子遗传学;
  • 关键词

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