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人类代谢组学中的基因组规模模型

Genome-scale models in human metabologenomics.

作者信息

Mardinoglu Adil, Palsson Bernhard Ø

机构信息

Science for Life Laboratory, KTH - Royal Institute of Technology, Stockholm, Sweden.

Centre for Host-Microbiome Interactions, Faculty of Dentistry, Oral and Craniofacial Sciences, King's College London, London, UK.

出版信息

Nat Rev Genet. 2025 Feb;26(2):123-140. doi: 10.1038/s41576-024-00768-0. Epub 2024 Sep 19.

Abstract

Metabologenomics integrates metabolomics with other omics data types to comprehensively study the genetic and environmental factors that influence metabolism. These multi-omics data can be incorporated into genome-scale metabolic models (GEMs), which are highly curated knowledge bases that explicitly account for genes, transcripts, proteins and metabolites. By including all known biochemical reactions catalysed by enzymes and transporters encoded in the human genome, GEMs analyse and predict the behaviour of complex metabolic networks. Continued advancements to the scale and scope of GEMs - from cells and tissues to microbiomes and the whole body - have helped to design effective treatments and develop better diagnostic tools for metabolic diseases. Furthermore, increasing amounts of multi-omics data are incorporated into GEMs to better identify the underlying mechanisms, biomarkers and potential drug targets of metabolic diseases.

摘要

代谢物基因组学将代谢组学与其他组学数据类型相结合,以全面研究影响代谢的遗传和环境因素。这些多组学数据可以整合到基因组规模的代谢模型(GEMs)中,GEMs是经过高度整理的知识库,明确考虑了基因、转录本、蛋白质和代谢物。通过纳入人类基因组中编码的酶和转运蛋白催化的所有已知生化反应,GEMs分析和预测复杂代谢网络的行为。GEMs在规模和范围上的不断进步——从细胞和组织到微生物群落和整个身体——有助于设计有效的治疗方法,并开发更好的代谢疾病诊断工具。此外,越来越多的多组学数据被整合到GEMs中,以更好地识别代谢疾病的潜在机制、生物标志物和潜在药物靶点。

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