Reverse engineering: a key component of systems biology to unravel global abiotic stress cross-talk

被引:28
作者
Friedel, Swetlana [1 ]
Usadel, Bjroen [2 ,3 ]
von Wiren, Nicolaus [1 ]
Sreenivasulu, Nese [1 ]
机构
[1] Leibniz Inst Plant Genet & Crop Plant Res, D-06466 Gatersleben, Germany
[2] Rhein Westfal TH Aachen, Aachen, Germany
[3] Forschungszentrum Julich, Inst Bio & Geosci, IBG Plant Sci 2, D-52425 Julich, Germany
关键词
abiotic stress; Arabidopsis; reverse engineering; systems biology; stress tolerance; yield;
D O I
10.3389/fpls.2012.00294
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Understanding the global abiotic stress response is an important stepping stone for the development of universal stress tolerance in plants in the era of climate change. Although co-occurrence of several stress factors (abiotic and biotic) in nature is found to be frequent, current attempts are poor to understand the complex physiological processes impacting plant growth under combinatory factors. In this review article, we discuss the recent advances of reverse engineering approaches that led to seminal discoveries of key candidate regulatory genes involved in cross-talk of abiotic stress responses and summarized the available tools of reverse engineering and its relevant application. Among the universally induced regulators involved in various abiotic stress responses, we highlight the importance of (i) abscisic acid (ABA) and jasmonic acid (JA) hormonal cross-talks and (ii) the central role of WRKY transcription factors (TF), potentially mediating both abiotic and biotic stress responses. Such interactome networks help not only to derive hypotheses but also play a vital role in identifying key regulatory targets and interconnected hormonal responses. To explore the full potential of gene network inference in the area of abiotic stress tolerance, we need to validate hypotheses by implementing time-dependent gene expression data from genetically engineered plants with modulated expression of target genes. We further propose to combine information on gene-by-gene interactions with data from physical interaction platforms such as protein protein or TF-gene networks.
引用
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页数:16
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