Regulation and functional roles revealed by clustering of microarray expression data of Escherichia coli genes.

IF 1.6 4区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Mishael Sánchez-Pérez, Humberto Peralta, M Cecilia Ishida-Guitierrez, Alberto Santos-Zavaleta, Irma Martínez-Flores, Faviola Tavares-Carreon, Cesaré Ovando-Vázquez
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引用次数: 0

Abstract

Microarray data can be used to identify co-expressed genes that may play a role in the same biological process. An enormous amount of gene expression data is currently available online in repositories for several organisms. Therefore, the analysis and interpretation of this information could help us organize, make sense and notice the knowledge that it contains which represents a major challenge in the postgenomic era. Here, we grouped genes of Escherichia coli K-12 via expression data to infer meaningful transcriptional regulatory information, namely functionally relevant clusters, which were validated with curated transcriptional regulatory information in RegulonDB. Our method is based on the assumption that co-expressed genes reflect functional units provided by their genetic structure, i.e. the arrangement of the genes, their regulation, and their participation in defined biological processes. We showed that co-expressed genes are involved in the same metabolic pathways and type of regulation (through transcription factors, σ-factors, allosteric regulation or microRNA regulation) and are helpful for identifying novel transcriptional regulatory interactions. .

大肠杆菌基因微阵列表达数据聚类揭示的调控及其功能作用。
微阵列数据可用于鉴定可能在相同生物过程中发挥作用的共表达基因。大量的基因表达数据目前可以在网上的存储库中获得。因此,对这些信息的分析和解释可以帮助我们组织、理解和注意到它所包含的知识,这代表了后基因组时代的一个主要挑战。在这里,我们通过表达数据对大肠杆菌K-12的基因进行分组,推断出有意义的转录调控信息,即功能相关的簇,并用RegulonDB中整理的转录调控信息进行验证。我们的方法是基于这样的假设,即共表达基因反映了其遗传结构提供的功能单位,即基因的排列,它们的调控,以及它们在确定的生物过程中的参与。我们发现,共表达基因参与相同的代谢途径和调节类型(通过转录因子,σ-因子,变构调节或microRNA调节),并有助于识别新的转录调节相互作用。 。
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来源期刊
Physical biology
Physical biology 生物-生物物理
CiteScore
4.20
自引率
0.00%
发文量
50
审稿时长
3 months
期刊介绍: Physical Biology publishes articles in the broad interdisciplinary field bridging biology with the physical sciences and engineering. This journal focuses on research in which quantitative approaches – experimental, theoretical and modeling – lead to new insights into biological systems at all scales of space and time, and all levels of organizational complexity. Physical Biology accepts contributions from a wide range of biological sub-fields, including topics such as: molecular biophysics, including single molecule studies, protein-protein and protein-DNA interactions subcellular structures, organelle dynamics, membranes, protein assemblies, chromosome structure intracellular processes, e.g. cytoskeleton dynamics, cellular transport, cell division systems biology, e.g. signaling, gene regulation and metabolic networks cells and their microenvironment, e.g. cell mechanics and motility, chemotaxis, extracellular matrix, biofilms cell-material interactions, e.g. biointerfaces, electrical stimulation and sensing, endocytosis cell-cell interactions, cell aggregates, organoids, tissues and organs developmental dynamics, including pattern formation and morphogenesis physical and evolutionary aspects of disease, e.g. cancer progression, amyloid formation neuronal systems, including information processing by networks, memory and learning population dynamics, ecology, and evolution collective action and emergence of collective phenomena.
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