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重新注释是功能基因组学数据系统生物学建模的一个重要步骤。

Re-annotation is an essential step in systems biology modeling of functional genomics data.

机构信息

Department of Basic Sciences, College of Veterinary Medicine, Mississippi State University, Starkville, Mississippi, United States of America.

出版信息

PLoS One. 2010 May 14;5(5):e10642. doi: 10.1371/journal.pone.0010642.

Abstract

One motivation of systems biology research is to understand gene functions and interactions from functional genomics data such as that derived from microarrays. Up-to-date structural and functional annotations of genes are an essential foundation of systems biology modeling. We propose that the first essential step in any systems biology modeling of functional genomics data, especially for species with recently sequenced genomes, is gene structural and functional re-annotation. To demonstrate the impact of such re-annotation, we structurally and functionally re-annotated a microarray developed, and previously used, as a tool for disease research. We quantified the impact of this re-annotation on the array based on the total numbers of structural- and functional-annotations, the Gene Annotation Quality (GAQ) score, and canonical pathway coverage. We next quantified the impact of re-annotation on systems biology modeling using a previously published experiment that used this microarray. We show that re-annotation improves the quantity and quality of structural- and functional-annotations, allows a more comprehensive Gene Ontology based modeling, and improves pathway coverage for both the whole array and a differentially expressed mRNA subset. Our results also demonstrate that re-annotation can result in a different knowledge outcome derived from previous published research findings. We propose that, because of this, re-annotation should be considered to be an essential first step for deriving value from functional genomics data.

摘要

系统生物学研究的一个动机是从功能基因组学数据(如微阵列数据)中理解基因功能和相互作用。最新的基因结构和功能注释是系统生物学建模的重要基础。我们提出,任何功能基因组学数据的系统生物学建模的第一步,特别是对于最近测序的基因组物种,是基因结构和功能重新注释。为了证明这种重新注释的影响,我们对一个微阵列进行了结构和功能重新注释,该微阵列是作为疾病研究工具开发并以前使用过的。我们根据结构和功能注释的总数、基因注释质量(GAQ)评分和规范途径覆盖度来量化这种重新注释对该阵列的影响。然后,我们使用先前发表的使用该微阵列的实验来量化重新注释对系统生物学建模的影响。我们表明,重新注释提高了结构和功能注释的数量和质量,允许更全面的基于基因本体论的建模,并提高了整个阵列和差异表达 mRNA 子集的途径覆盖度。我们的结果还表明,重新注释可能会导致从以前发表的研究结果中得出不同的知识结果。我们提出,由于这个原因,重新注释应该被视为从功能基因组学数据中获取价值的必要的第一步。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/88a6/2871057/b8fc501bb6ef/pone.0010642.g001.jpg

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