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Deciphering transcriptional regulatory elements that encode specific cell cycle phasing by comparative genomics analysis.

机译:通过比较基因组学分析来破译编码特定细胞周期阶段的转录调控元件。

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Transcriptional regulation is a major tier in the periodic engine that mobilizes cell cycle progression. The availability of complete genome sequences of multiple organisms holds promise for significantly improving the specificity of computational identification of functional elements. Here, we applied a comparative genomics analysis to decipher transcriptional regulatory elements that control cell cycle phasing. We analyzed genome-wide promoter sequences from 12 organisms, including worm, fly, fish, rodents and human, and identified conserved transcriptional modules that determine the expression of genes in specific cell cycle phases. We demonstrate that a canonical E2F signal encodes for expression highly specific to the G1/S phase, and that a cis-regulatory module comprising CHR-NF-Y elements dictates expression that is restricted to the G2 and G2/M phases. B-Myb binding site signatures occur in many of the CHR-NF-Y target genes, suggesting a specific role for this triplet in the regulation of the cell cycle transcriptional program. Remarkably, E2F signals are conserved in promoters of G1/S genes in all organisms from worm to human. The CHR-NF-Y module is conserved in promoters of G2/M regulated genes in all analyzed vertebrates. Our results reveal novel modules that determine specific cell cycle phasing, and identify their respective putative target genes with remarkably high specificity.
机译:转录调节是周期性引擎中的主要层,它可动员细胞周期进程。多种生物的完整基因组序列的可用性有望显着提高功能元件计算鉴定的特异性。在这里,我们应用了比较基因组学分析来破译控制细胞周期定相的转录调控元件。我们分析了来自12种生物的全基因组启动子序列,包括蠕虫,苍蝇,鱼,啮齿动物和人类,并确定了确定基因在特定细胞周期阶段表达的保守转录模块。我们证明规范的E2F信号编码的表达高度特异于G1 / S期,并且包含CHR-NF-Y元素的顺式调控模块决定了仅限于G2和G2 / M期的表达。 B-Myb结合位点签名出现在许多CHR-NF-Y靶基因中,表明该三联体在调节细胞周期转录程序中具有特定作用。值得注意的是,E2F信号在从蠕虫到人的所有生物中均在G1 / S基因的启动子中保守。在所有分析的脊椎动物中,CHR-NF-Y模块在G2 / M调控基因的启动子中均保守。我们的结果揭示了新颖的模块,这些模块可确定特定的细胞周期定相,并以非常高的特异性鉴定各自的推定靶基因。

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