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网络引导的广泛转录因子间的上位性在参与脂肪族硫代葡萄糖苷生物合成中的发现。

Network-Guided Discovery of Extensive Epistasis between Transcription Factors Involved in Aliphatic Glucosinolate Biosynthesis.

机构信息

Department of Plant Sciences, University of California, Davis, Davis, California 95616.

Department of Plant Biology and Genome Center, University of California, Davis, Davis, California 95616.

出版信息

Plant Cell. 2018 Jan;30(1):178-195. doi: 10.1105/tpc.17.00805. Epub 2018 Jan 9.

Abstract

Plants use diverse mechanisms influenced by vast regulatory networks of indefinite scale to adapt to their environment. These regulatory networks have an unknown potential for epistasis between genes within and across networks. To test for epistasis within an adaptive trait genetic network, we generated and tested 47 double mutant combinations for 20 transcription factors, which all influence the accumulation of aliphatic glucosinolates, the defense metabolites that control fitness. The epistatic combinations were used to test if there is more or less epistasis depending on gene membership within the same or different phenotypic subnetworks. Extensive epistasis was observed between the transcription factors, regardless of subnetwork membership. Metabolite accumulation displayed antagonistic epistasis, suggesting the presence of a buffering mechanism. Epistasis affecting enzymatic estimated activity was highly conditional on the tissue and environment and shifted between both antagonistic and synergistic forms. Transcriptional analysis showed that epistasis shifts depend on how the trait is measured. Because the 47 combinations described here represent a small sampling of the potential epistatic combinations in this genetic network, there is potential for significantly more epistasis. Additionally, the main effect of the individual gene was not predictive of the epistatic effects, suggesting that there is a need for further studies.

摘要

植物利用受广泛的、规模不定的调控网络影响的多种机制来适应环境。这些调控网络在基因间存在未知的上位性潜力,无论是在同一网络内还是不同网络之间。为了在适应性特征遗传网络中检测上位性,我们生成并测试了 20 个转录因子的 47 个双突变组合,这些转录因子都影响控制适应性的脂肪族硫代葡萄糖苷的积累。这些上位性组合用于测试同一或不同表型子网内的基因成员是否存在更多或更少的上位性。转录因子之间存在广泛的上位性,无论子网成员如何。代谢物积累表现出拮抗上位性,表明存在缓冲机制。影响酶估计活性的上位性高度依赖于组织和环境,并在拮抗和协同两种形式之间转换。转录分析表明,上位性的转变取决于如何测量性状。由于这里描述的 47 种组合仅代表该遗传网络中潜在上位性组合的一小部分,因此可能存在更多的上位性。此外,单个基因的主要效应不能预测上位性效应,这表明需要进一步研究。

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