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  • 标题:Gene regulatory network inference in long-lived C. elegans reveals modular properties that are predictive of novel aging genes
  • 本地全文:下载
  • 作者:Manusnan Suriyalaksh ; Celia Raimondi ; Abraham Mains
  • 期刊名称:iScience
  • 印刷版ISSN:2589-0042
  • 出版年度:2022
  • 卷号:25
  • 期号:1
  • 页码:1-40
  • DOI:10.1016/j.isci.2021.103663
  • 语种:English
  • 出版社:Elsevier
  • 摘要:SummaryWe design a “wisdom-of-the-crowds” GRN inference pipeline and couple it to complex network analysis to understand the organizational principles governing gene regulation in long-livedglp-1/NotchCaenorhabditis elegans. The GRN has three layers (input, core, and output) and is topologically equivalent to bow-tie/hourglass structures prevalent among metabolic networks. To assess the functional importance of structural layers, we screened 80% of regulators and discovered 50 new aging genes, 86% with human orthologues. Genes essential for longevity—including ones involved in insulin-like signaling (ILS)—are at the core, indicating that GRN's structure is predictive of functionality. We usedin vivoreporters and a novel functional network covering 5,497 genetic interactions to make mechanistic predictions. We used genetic epistasis to test some of these predictions, uncovering a novel transcriptional regulator,sup-37, that works alongside DAF-16/FOXO. We present a framework with predictive power that can accelerate discovery inC. elegansand potentially humans.Graphical abstractDisplay OmittedHighlights•Gene-regulatory inference provides global network of long-lived animals•The large-scale topology of the network has an hourglass structure•Membership to the core of the hourglass is a good predictor of functionality•Discovered 50 novel aging genes, includingsup-37, a DAF-16 dependent geneGenetics; Genomics; Bioinformatics
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