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Inhibition of the binding of MSG-intermolt-specific complex, MIC, to the sericin-1 gene promoter and sericin-1 gene expression by POU-M1/SGF-3

机译:POU-M1 / SGF-3抑制味精-肠溶质特异性复合物MIC与sericin-1基因启动子和sericin-1基因表达的结合

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The sericin-1 gene encoding a glue protein is expressed in the middle silk gland (MSG) of the silkworm, Bombyx mori. A member of the class III POU domain transcription factors, POU-M1, was cloned as the factor bound to the SC site of the sericin-1 promoter and has been proposed to be a positive transcription factor. In this study, we analyzed the expression pattern of the POU-M1 gene in fourth and fifth instars in comparison with the pattern of the sericin-1 gene. The POU-M1 gene was expressed strongly in the region anterior to the sericin-1-expressing portion of the silk gland at both feeding stages. As the sericin-1-expressing region expands from the posterior to middle portions of the MSG in the fifth instar, the POU-M1-expressing region retreated from the middle to anterior portion. Introduction of the expression vector of POU-M1 into the silk glands by gene gun technology repressed promoter activity of the sericin-1 gene, suggesting that POU-M1 regulates the sericin-1 gene negatively. An in vitro binding assay showed that POU-M1 bound not only to the SC site but also to other promoter elements newly detected in vivo. Another spatiotemporal specific factor MIC binds to these elements, and POU-M1 competed with MIC to bind at the −70 site essential for promoter activity. These results suggest that POU-M1 is involved in restricting the anterior boundary of the sericin-1-expressing region in the silk gland by inhibiting the binding of the transcriptional activator to the promoter elements.
机译:编码胶蛋白的丝胶蛋白1基因在蚕Bombyx mori的中间丝腺(MSG)中表达。已将III类POU结构域转录因子POU-M1的成员克隆为与sericin-1启动子的SC位点结合的因子,并已提出将其作为阳性转录因子。在这项研究中,我们分析了POU-M1基因在第四和第五龄幼虫中的表达模式,与sericin-1基因的模式相比。在两个进食阶段,POU-M1基因在丝腺表达Sricin-1的部分之前的区域强烈表达。随着表达Sricin-1的区域从第五龄期的MSG的后部扩展到中部,POU-M1的表达区从中部退回到前部。通过基因枪技术将POU-M1表达载体导入丝腺抑制了Sericin-1基因的启动子活性,这表明POU-M1对Sericin-1基因有负调节作用。体外结合试验显示,POU-M1不仅与SC位点结合,而且还与体内新发现的其他启动子元件结合。另一个时空特异性因子MIC与这些元素结合,POU-M1与MIC竞争在启动子活性必不可少的-70位点结合。这些结果表明,POU-M1通过抑制转录激活因子与启动子元件的结合,参与了丝腺丝胶蛋白-1表达区域的前边界的限制。

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