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首页> 外文期刊>Advances in Bioscience and Biotechnology >Analysis of the Promoter Region, Motif and CpG Islands in AraC Family Transcriptional Regulator ACP92 Genes of &i&Herbaspirillum seropedicae&/i&
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Analysis of the Promoter Region, Motif and CpG Islands in AraC Family Transcriptional Regulator ACP92 Genes of &i&Herbaspirillum seropedicae&/i&

机译:螺旋藻螺旋体的AraC家族转录调节子ACP92基因的启动子区域,基序和CpG岛的分析。

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摘要

Identification of promoters and their regulatory elements are the most important phases in bioinformatics. To understand the regulation of gene expression, identification, and analysis of promoters region, motif and CpG islands are the most important steps. The accurate prediction of promoter’s is basic for proper interpretation of gene expression patterns, construction and understanding of genetic regulatory system. Therefore, the objective of this study was to analy ze the promoter region, motif such as a transcription factor and CpG islands in AraC family transcriptional regulator ACP92 genes of Herbaspirillum seropedicae . The analysis was carried out by identifying transcription start sites in ACP92 genome sequences taken from the H . seropedicae assembly of NCBI genome browser, and 29 ACP92 genes sequences. Accordingly, transcription start sites (TSS) were identified, and the result indicated that 37.9% ha d more than one TSS whereas only 62.1% had one TSS. In the analysis, seven motifs were identified from the thought sequences and MV6 was revealed the common promoter motif for all (100%) in H. seropedicae ACP92 gene that serves as binding sites for transcription factors which shared a minimum of 48.27%. Based on a common motif MV6 to find out similar motifs using TOMTOM from the databases of prokaryotes DNA, most of them are transcription factors of fur family. The others are bacterial histone-like protein family, matp and sigma-54 factor family also transcription factor families that are binding candidate to MV6. H. seropedicae ACP92 genes are CpG Island which implies that the regulation of gene expression plays an important role.
机译:启动子及其调控元件的鉴定是生物信息学中最重要的阶段。要了解基因表达的调控,启动子区域,基序和CpG岛的鉴定和分析是最重要的步骤。对启动子的准确预测是正确解释基因表达模式,构建和理解遗传调控系统的基础。因此,本研究的目的是分析草拟螺旋藻的AraC家族转录调节因子ACP92基因的启动子区域,基序,例如转录因子和CpG岛。通过鉴定取自 H 的ACP92基因组序列中的转录起始位点进行分析。 NCBI基因组浏览器的Seropedicae装配体和29个ACP92基因序列。因此,鉴定出转录起始位点(TSS),结果表明37.9%具有一个以上的TSS,而只有62.1%具有一个TSS。在分析中,从思维序列中鉴定出七个基序,并且MV6揭示了浆膜嗜血杆菌ACP92基因中所有(100%)共同的启动子基序,它们是转录因子的结合位点,其共享最小比例为48.27% 。基于共同的基序MV6,使用TOMTOM从原核生物DNA数据库中发现相似的基序,其中大多数是毛皮家族的转录因子。其他是细菌组蛋白样蛋白家族,matp和sigma-54因子家族,也是与MV6结合的候选转录因子家族。猪嗜血杆菌ACP92基因是CpG岛,这表明基因表达的调控起着重要作用。

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