基因敲除后,进化酵母菌株的转录组逐渐发生变化。

IF 4.6 2区 综合性期刊 Q1 MULTIDISCIPLINARY SCIENCES
iScience Pub Date : 2024-10-21 eCollection Date: 2024-11-15 DOI:10.1016/j.isci.2024.111219
Bei Jiang, Chuyao Xiao, Li Liu
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引用次数: 0

摘要

基因敲除会破坏细胞平衡,改变基因表达和表型。我们通过对hap4Δ和ade1Δ酵母菌株进行适应性进化实验,研究细胞是否会恢复到基因敲除前的转录组状态。分析表明,野生型菌株中表达水平较高、物理相互作用伙伴较多的基因更有可能被恢复,这表明具有重要功能的基因对遗传扰动的恢复能力更强。然而,随着实验的进行,大多数最初恢复的基因变得不再恢复。基因敲除菌株中超过 60% 的差异表达基因在进化菌株中仍未恢复。进化菌株表现出不同的转录组状态,并随着时间的推移与原始菌株发生分化。在进化过程中,核糖体生物发生成分呈现出系统性的序列变化。我们的研究结果表明,即使经过 28 天的培养,基因敲除菌株的转录组也很难恢复到原始状态。相反,补偿机制导致了不同的次优状态,凸显了遗传扰动后复杂的转录组动态变化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Progressive transcriptomic shifts in evolved yeast strains following gene knockout.

Gene knockout disrupts cellular homeostasis, altering gene expression, and phenotypes. We investigated whether cells return to their pre-knockout transcriptomic state through adaptive evolution experiments on hap4Δ and ade1Δ yeast strains. Analysis revealed that genes with higher expression levels and more physical interaction partners in wild-type strains were more likely to be restored, suggesting that genes of significant functional importance have increased resilience to genetic perturbations. However, as the experiment progressed, most initially restored genes became unrestored. Over 60% of differentially expressed genes in knockout strains remained unrestored in evolved strains. Evolved strains exhibited distinct transcriptomic states, diverging from the original strain over time. Ribosome biogenesis components exhibited systematic sequential changes during the evolution. Our findings suggest the knockout strain transcriptomes struggle to return to the original state even after 28 days of culture. Instead, compensatory mechanisms lead to distinct suboptimal states, highlighting the complex transcriptomic dynamics following genetic perturbations.

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来源期刊
iScience
iScience Multidisciplinary-Multidisciplinary
CiteScore
7.20
自引率
1.70%
发文量
1972
审稿时长
6 weeks
期刊介绍: Science has many big remaining questions. To address them, we will need to work collaboratively and across disciplines. The goal of iScience is to help fuel that type of interdisciplinary thinking. iScience is a new open-access journal from Cell Press that provides a platform for original research in the life, physical, and earth sciences. The primary criterion for publication in iScience is a significant contribution to a relevant field combined with robust results and underlying methodology. The advances appearing in iScience include both fundamental and applied investigations across this interdisciplinary range of topic areas. To support transparency in scientific investigation, we are happy to consider replication studies and papers that describe negative results. We know you want your work to be published quickly and to be widely visible within your community and beyond. With the strong international reputation of Cell Press behind it, publication in iScience will help your work garner the attention and recognition it merits. Like all Cell Press journals, iScience prioritizes rapid publication. Our editorial team pays special attention to high-quality author service and to efficient, clear-cut decisions based on the information available within the manuscript. iScience taps into the expertise across Cell Press journals and selected partners to inform our editorial decisions and help publish your science in a timely and seamless way.
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