Institute of Science and Technology Austria, Klosterneuburg, Austria.
Department of Microbiology, Immunobiology and Genetics, Max F. Perutz Laboratories, Center Of Molecular Biology, University of Vienna, Vienna, Austria.
Elife. 2021 Mar 8;10:e65993. doi: 10.7554/eLife.65993.
Gene expression levels are influenced by multiple coexisting molecular mechanisms. Some of these interactions such as those of transcription factors and promoters have been studied extensively. However, predicting phenotypes of gene regulatory networks (GRNs) remains a major challenge. Here, we use a well-defined synthetic GRN to study in how network phenotypes depend on local genetic context, i.e. the genetic neighborhood of a transcription factor and its relative position. We show that one GRN with fixed topology can display not only quantitatively but also qualitatively different phenotypes, depending solely on the local genetic context of its components. Transcriptional read-through is the main molecular mechanism that places one transcriptional unit (TU) within two separate regulons without the need for complex regulatory sequences. We propose that relative order of individual TUs, with its potential for combinatorial complexity, plays an important role in shaping phenotypes of GRNs.
基因表达水平受到多种共存的分子机制的影响。其中一些相互作用,如转录因子和启动子的相互作用,已经得到了广泛的研究。然而,预测基因调控网络 (GRN) 的表型仍然是一个主要的挑战。在这里,我们使用一个定义明确的合成 GRN 来研究网络表型如何取决于局部遗传背景,即转录因子及其相对位置的遗传邻域。我们表明,一个具有固定拓扑的 GRN 不仅可以显示出不同的数量表现,而且可以显示出不同的质量表现,这完全取决于其组成部分的局部遗传背景。转录通读是将一个转录单元 (TU) 放置在两个单独的调控子中而不需要复杂的调节序列的主要分子机制。我们提出,单个 TU 的相对顺序,及其组合复杂性的潜力,在塑造 GRN 的表型方面起着重要的作用。
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