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利用信息论模型发现大肠杆菌中的Fur结合位点簇。

Discovery of Fur binding site clusters in Escherichia coli by information theory models.

作者信息

Chen Zehua, Lewis Karen A, Shultzaberger Ryan K, Lyakhov Ilya G, Zheng Ming, Doan Bernard, Storz Gisela, Schneider Thomas D

机构信息

National Cancer Institute at Frederick, Center for Cancer Research Nanobiology Program, Basic Research Program, SAIC-Frederick, Inc., Frederick, MD 21702-1201, USA.

出版信息

Nucleic Acids Res. 2007;35(20):6762-77. doi: 10.1093/nar/gkm631. Epub 2007 Oct 5.

Abstract

Fur is a DNA binding protein that represses bacterial iron uptake systems. Eleven footprinted Escherichia coli Fur binding sites were used to create an initial information theory model of Fur binding, which was then refined by adding 13 experimentally confirmed sites. When the refined model was scanned across all available footprinted sequences, sequence walkers, which are visual depictions of predicted binding sites, frequently appeared in clusters that fit the footprints ( approximately 83% coverage). This indicated that the model can accurately predict Fur binding. Within the clusters, individual walkers were separated from their neighbors by exactly 3 or 6 bases, consistent with models in which Fur dimers bind on different faces of the DNA helix. When the E. coli genome was scanned, we found 363 unique clusters, which includes all known Fur-repressed genes that are involved in iron metabolism. In contrast, only a few of the known Fur-activated genes have predicted Fur binding sites at their promoters. These observations suggest that Fur is either a direct repressor or an indirect activator. The Pseudomonas aeruginosa and Bacillus subtilis Fur models are highly similar to the E. coli Fur model, suggesting that the Fur-DNA recognition mechanism may be conserved for even distantly related bacteria.

摘要

Fur是一种抑制细菌铁摄取系统的DNA结合蛋白。利用11个有足迹的大肠杆菌Fur结合位点创建了Fur结合的初始信息论模型,随后通过添加13个经实验证实的位点对其进行了优化。当在所有可用的有足迹序列上扫描优化后的模型时,序列步行者(预测结合位点的直观描绘)经常出现在与足迹相符的簇中(覆盖率约为83%)。这表明该模型能够准确预测Fur结合。在这些簇中,各个步行者与其相邻者之间精确相隔3个或6个碱基,这与Fur二聚体结合在DNA螺旋不同面上的模型一致。当扫描大肠杆菌基因组时,我们发现了363个独特的簇,其中包括所有已知的参与铁代谢的受Fur抑制的基因。相比之下,只有少数已知的受Fur激活的基因在其启动子处有预测的Fur结合位点。这些观察结果表明,Fur要么是直接阻遏物,要么是间接激活剂。铜绿假单胞菌和枯草芽孢杆菌的Fur模型与大肠杆菌的Fur模型高度相似,这表明即使是亲缘关系较远的细菌,Fur-DNA识别机制也可能是保守的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/697b/2189734/15b51bf485e3/gkm631f1.jpg

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