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基于Affymetrix基因芯片的结核分枝杆菌基因表达数据为调控基因和假设基因提供了深入见解。

The gene expression data of Mycobacterium tuberculosis based on Affymetrix gene chips provide insight into regulatory and hypothetical genes.

作者信息

Fu Li M, Fu-Liu Casey S

机构信息

Pacific Tuberculosis and Cancer Research Organization, Irvine, California, USA.

出版信息

BMC Microbiol. 2007 May 14;7:37. doi: 10.1186/1471-2180-7-37.

Abstract

BACKGROUND

Tuberculosis remains a leading infectious disease with global public health threat. Its control and management have been complicated by multi-drug resistance and latent infection, which prompts scientists to find new and more effective drugs. With the completion of the genome sequence of the etiologic bacterium, Mycobacterium tuberculosis, it is now feasible to search for new drug targets by sieving through a large number of gene products and conduct genome-scale experiments based on microarray technology. However, the full potential of genome-wide microarray analysis in configuring interrelationships among all genes in M. tuberculosis has yet to be realized. To date, it is only possible to assign a function to 52% of proteins predicted in the genome.

RESULTS

We conducted a functional-genomics study using the high-resolution Affymetrix oligonucleotide GeneChip. Approximately one-half of the genes were found to be always expressed, including more than 100 predicted conserved hypotheticals, in the genome of M. tuberculosis during the log phase of in vitro growth. The gene expression profiles were analyzed and visualized through cluster analysis to epitomize the full details of genomic behavior. Broad patterns derived from genome-wide expression experiments in this study have provided insight into the interrelationships among genes in the basic cellular processes of M. tuberculosis.

CONCLUSION

Our results have confirmed several known gene clusters in energy production, information pathways, and lipid metabolism, and also hinted at potential roles of hypothetical and regulatory proteins.

摘要

背景

结核病仍然是一种对全球公共卫生构成威胁的主要传染病。其控制和管理因多重耐药性和潜伏感染而变得复杂,这促使科学家寻找新的更有效的药物。随着致病细菌结核分枝杆菌基因组序列的完成,现在通过筛选大量基因产物来寻找新的药物靶点并基于微阵列技术进行基因组规模的实验成为可能。然而,全基因组微阵列分析在构建结核分枝杆菌所有基因之间相互关系方面的全部潜力尚未实现。迄今为止,仅能为基因组中预测的52%的蛋白质赋予功能。

结果

我们使用高分辨率的Affymetrix寡核苷酸基因芯片进行了一项功能基因组学研究。在体外生长的对数期,发现结核分枝杆菌基因组中约一半的基因始终表达,包括100多个预测的保守假设蛋白。通过聚类分析对基因表达谱进行分析和可视化,以概括基因组行为的全部细节。本研究中全基因组表达实验得出的广泛模式为了解结核分枝杆菌基本细胞过程中基因之间的相互关系提供了线索。

结论

我们的结果证实了能量产生、信息途径和脂质代谢中的几个已知基因簇,也暗示了假设蛋白和调节蛋白的潜在作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aab0/1884158/0cd85b80a57b/1471-2180-7-37-1.jpg

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