首页> 美国卫生研究院文献>Plant Physiology >Focus Issue on Light Signaling: Identification of Promoter Motifs Involved in the Network of Phytochrome A-Regulated Gene Expression by Combined Analysis of Genomic Sequence and Microarray Data
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Focus Issue on Light Signaling: Identification of Promoter Motifs Involved in the Network of Phytochrome A-Regulated Gene Expression by Combined Analysis of Genomic Sequence and Microarray Data

机译:关于光信号的焦点问题:通过基因组序列和微阵列数据的组合分析鉴定参与植物色素A调控的基因表达网络的启动子基序

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摘要

Several hundred Arabidopsis genes, transcriptionally regulated by phytochrome A (phyA), were previously identified using an oligonucleotide microarray. We have now identified, in silico, conserved sequence motifs in the promoters of these genes by comparing the promoter sequences to those of all the genes present on the microarray from which they were sampled. This was done using a Perl script (called Sift) that identifies over-represented motifs using an enumerative approach. The utility of Sift was verified by analysis of circadian-regulated promoters known to contain a biologically significant motif. Several elements were then identified in phyA-responsive promoters by their over-representation. Five previously undescribed motifs were detected in the promoters of phyA-induced genes. Four novel motifs were found in phyA-repressed promoters, plus a motif that strongly resembles the DE1 element. The G-box, CACGTG, was a prominent hit in both induced and repressed phyA-responsive promoters. Intriguingly, two distinct flanking consensus sequences were observed adjacent to the G-box core sequence: one predominating in phyA-induced promoters, the other in phyA-repressed promoters. Such different conserved flanking nucleotides around the core motif in these two sets of promoters may indicate that different members of the same family of DNA-binding proteins mediate phyA induction and repression. An increased abundance of G-box sequences was observed in the most rapidly phyA-responsive genes and in the promoters of phyA-regulated transcription factors, indicating that G-box-binding transcription factors are upstream components in a transcriptional cascade that mediates phyA-regulated development.
机译:以前使用寡核苷酸微阵列鉴定了受植物色素A(phyA)转录调控的数百个拟南芥基因。现在,我们已经通过比较启动子序列与从其取样的微阵列上存在的所有基因的启动子序列,在计算机上鉴定了这些基因的启动子中的保守序列基序。这是使用Perl脚本(称为Sift)完成的,该脚本使用枚举方法来识别过度代表的主题。通过对已知包含生物学上重要基序的昼夜节律调节的启动子进行分析,验证了Sift的实用性。然后通过phyA响应启动子的过量表达鉴定出几种元素。在phyA诱导的基因启动子中检测到五个先前未描述的基序。在phyA抑制的启动子中发现了四个新颖的​​基序,以及一个与DE1元件非常相似的基序。 G-box CACGTG在诱导和抑制的phyA反应性启动子中均是突出的表现。有趣的是,在G-box核心序列附近观察到两个不同的侧翼共有序列:一个在phyA诱导的启动子中占主导,另一个在phyA抑制的启动子中占主导。在这两套启动子中,核心基序周围的这种不同的保守侧翼核苷酸可能表明同一DNA结合蛋白家族的不同成员介导了phyA诱导和抑制。在最快速的phyA响应基因和phyA调控的转录因子启动子中观察到G-box序列的丰度增加,表明G-box结合转录因子是介导phyA调控的转录级联的上游成分。发展。

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