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首页> 外文期刊>Nucleic Acids Research >Unique organization and involvement of GAGA factors in transcriptional regulation of the Xenopus stromelysin-3 gene.
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Unique organization and involvement of GAGA factors in transcriptional regulation of the Xenopus stromelysin-3 gene.

机译:GAGA因子在非洲爪蟾stromelysin-3基因的转录调控中的独特组织和参与。

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摘要

Expression of the matrix metalloproteinase (MMP) gene stromelysin-3 ( ST3 ) has been shown to be tightly associated with cell migration and apoptosis inmammals and amphibians. This contrasts with most other MMP genes. We demonstrate here that the Xenopus ST3 gene also has a structure distinct from other MMP genes, with its C-terminal half (the hemopexin domain) encoded by 4 instead of 6 exons, as in other MMP genes. Our primer extension analysis reveals the existence of two transcription start sites and at least one is needed for transcription of the promoter in transient transfection assays. Furthermore, our deletion analysis has demonstrated a requirement for at least one GAGA factor binding site for promoter function. In vitro DNA binding and mutational studies have provided strong evidence for the participation of GAGA or GAGA-like factors in transcriptional regulation of the frog ST3 gene. This contrasts with regulation of the human ST3 promoter. These results suggest that the ST3 gene evolved prior to most other metalloproteinase genes and uses distinct regulation pathways to achieve similar expression profiles and serve similar functions in mammals and amphibians.
机译:基质金属蛋白酶(MMP)基因stromelysin-3(ST3)的表达已被证明与哺乳动物和两栖动物的细胞迁移和凋亡密切相关。这与大多数其他MMP基因形成对比。我们在这里证明,非洲爪蟾ST3基因也具有不同于其他MMP基因的结构,其C末端的一半(血凝素域)由4个而不是6个外显子编码,就像在其他MMP基因中一样。我们的引物延伸分析揭示了两个转录起始位点的存在,并且在瞬时转染测定中至少需要一个用于启动子的转录。此外,我们的缺失分析表明启动子功能需要至少一个GAGA因子结合位点。体外DNA结合和突变研究为GAGA或类GAGA因子参与青蛙ST3基因的转录调控提供了有力的证据。这与人ST3启动子的调节相反。这些结果表明,ST3基因先于大多数其他金属蛋白酶基因进化,并使用不同的调控途径在哺乳动物和两栖动物中实现相似的表达谱并发挥相似的功能。

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