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通过与不同分类亚组进行比较基因组学来预测植物乳杆菌的顺式作用元件。

Predicting cis-acting elements of Lactobacillus plantarum by comparative genomics with different taxonomic subgroups.

作者信息

Wels Michiel, Francke Christof, Kerkhoven Robert, Kleerebezem Michiel, Siezen Roland J

机构信息

Wageningen Centre for Food Sciences, PO Box 557, 6700 AN Wageningen, The Netherlands.

出版信息

Nucleic Acids Res. 2006 Apr 13;34(7):1947-58. doi: 10.1093/nar/gkl138. Print 2006.

Abstract

Cis-acting elements in Lactobacillus plantarum were predicted by comparative analysis of the upstream regions of conserved genes and predicted transcriptional units (TUs) in different bacterial genomes. TUs were predicted for two species sets, with different evolutionary distances to L.plantarum. TUs were designated 'cluster of orthologous transcriptional units' (COT) when >50% of the genes were orthologous in different species. Conserved DNA sequences were detected in the upstream regions of different COTs. Subsequently, conserved motifs were used to scan upstream regions of all TUs. This method revealed 18 regulatory motifs only present in lactic acid bacteria (LAB). The 18 LAB-specific candidate regulatory motifs included 13 that were not described previously. These LAB-specific different motifs were found in front of genes encoding functions varying from cold shock proteins to RNA and DNA polymerases, and many unknown functions. The best-described LAB-specific motif found was the CopR-binding site, regulating expression of copper transport ATPases. Finally, all detected motifs were used to predict co-regulated TUs (regulons) for L.plantarum, and transcriptome profiling data were analyzed to provide regulon prediction validation. It is demonstrated that phylogenetic footprinting using different species sets can identify and distinguish between general regulatory motifs and LAB-specific regulatory motifs.

摘要

通过对不同细菌基因组中保守基因和预测转录单元(TU)的上游区域进行比较分析,预测了植物乳杆菌中的顺式作用元件。针对与植物乳杆菌进化距离不同的两个物种集预测了TU。当不同物种中>50%的基因是直系同源时,TU被指定为“直系同源转录单元簇”(COT)。在不同COT的上游区域检测到保守的DNA序列。随后,使用保守基序扫描所有TU的上游区域。该方法揭示了仅存在于乳酸菌(LAB)中的18个调控基序。这18个LAB特异性候选调控基序包括13个以前未描述过的基序。这些LAB特异性不同基序存在于编码从冷休克蛋白到RNA和DNA聚合酶等各种功能以及许多未知功能的基因之前。发现的描述最清楚的LAB特异性基序是CopR结合位点,它调节铜转运ATP酶的表达。最后,所有检测到的基序用于预测植物乳杆菌的共调控TU(调控子),并分析转录组谱数据以提供调控子预测验证。结果表明,使用不同物种集的系统发育足迹法可以识别和区分一般调控基序和LAB特异性调控基序。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a49/1435977/d13473849ffd/gkl138f1.jpg

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