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首页> 外文期刊>BMC Molecular Biology >Two non-homologous brain diseases-related genes, SERPINI1 and PDCD10, are tightly linked by an asymmetric bidirectional promoter in an evolutionarily conserved manner
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Two non-homologous brain diseases-related genes, SERPINI1 and PDCD10, are tightly linked by an asymmetric bidirectional promoter in an evolutionarily conserved manner

机译:两个非同源性脑疾病相关基因SERPINI1和PDCD10,通过不对称双向启动子以进化保守的方式紧密连接

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Background Despite of the fact that mammalian genomes are far more spacious than prokaryotic genomes, recent nucleotide sequencing data have revealed that many mammalian genes are arranged in a head-to-head orientation and separated by a small intergenic sequence. Extensive studies on some of these neighboring genes, in particular homologous gene pairs, have shown that these genes are often co-expressed in a symmetric manner and regulated by a shared promoter region. Here we report the identification of two non-homologous brain disease-related genes, with one coding for a serine protease inhibitor (SERPINI1) and the other for a programmed cell death-related gene (PDCD10), being tightly linked together by an asymmetric bidirectional promoter in an evolutionarily conserved fashion. This asymmetric bidirectional promoter, in cooperation with some cis-acting elements, is responsible for the co-regulation of the gene expression pattern as well as the tissue specificity of SERPINI1 and PDCD10. Results While SERPINI1 is predominantly expressed in normal brain and down-regulated in brain tumors, PDCD10 is ubiquitously expressed in all normal tissues but its gene transcription becomes aberrant in different types of cancers. By measuring the luciferase activity in various cell lysates, their 851-bp intergenic sequence was shown to be capable of driving the reporter gene expression in either direction. A 175-bp fragment from nt 1 to 175 in the vicinity of PDCD10 was further determined to function as a minimal bidirectional promoter. A critical regulatory fragment, from nt 176-473 outside the minimal promoter in the intergenic region, was identified to contain a strong repressive element for SERPINI1 and an enhancer for PDCD10. These cis-acting elements may exist to help coordinate the expression and regulation of the two flanking genes. Conclusion For all non-homologous genes that have been described to be closely adjacent in the mammalian genomes, the intergenic region of the head-to-head PDCD10-SERPINI1 gene pair provides an interesting and informative example of a complex regulatory system that governs the expression of both genes not only through an asymmetric bidirectional promoter, but also through fine-tuned regulations with some cis-acting elements.
机译:背景技术尽管事实上哺乳动物基因组比原核基因组要宽敞得多,但最近的核苷酸测序数据表明,许多哺乳动物基因以头对头的方向排列,并被一个小的基因间序列隔开。对这些邻近基因中的一些,特别是同源基因对的广泛研究表明,这些基因通常以对称方式共表达,并由一个共同的启动子区域调节。在这里,我们报告鉴定两个非同源性脑疾病相关基因,其中一个编码丝氨酸蛋白酶抑制剂(SERPINI1),另一个编码程序性细胞死亡相关基因(PDCD10),它们通过不对称双向紧密连接在一起进化上保守的启动子。这种不对称的双向启动子与一些顺式作用元件协同作用,共同调控基因表达模式以及SERPINI1和PDCD10的组织特异性。结果虽然SERPINI1主要在正常大脑中表达,并在脑肿瘤中下调,但PDCD10在所有正常组织中都普遍表达,但其基因转录在不同类型的癌症中变得异常。通过测量各种细胞裂解物中的萤光素酶活性,显示了它们的851-bp基因间序列能够在任一方向上驱动报告基因的表达。在PDCD10附近,从nt 1至175的175bp片段被进一步确定起最小双向启动子的作用。一个关键的调控片段,来自基因间区域最小启动子外的第176-473位核苷酸,被鉴定为包含一个对SERPINI1的强阻遏元件和一个PDCD10的增强子。这些顺式作用元件可能存在以帮助协调两个侧翼基因的表达和调控。结论对于已被描述为在哺乳动物基因组中紧密相邻的所有非同源基因,头对头PDCD10-SERPINI1基因对的基因间区域为控制表达的复杂调控系统提供了一个有趣且有意义的例子。不仅通过不对称的双向启动子,而且还通过带有一些顺式作用元件的精细调控来调节两个基因。

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