Dramatic genome-wide reprogramming of mRNA in hypometabolic muscle

IF 16.4 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY Accounts of Chemical Research Pub Date : 2024-02-13 DOI:10.1016/j.cbpb.2024.110952
Nicholas J. Hudson , Rebecca L. Cramp , Craig E. Franklin
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Abstract

In response to seasonal droughts, the green striped burrowing frog Cyclorana alboguttata enters a reversible hypometabolic state called aestivation where heart rate and oxygen consumption can be reduced despite warm (>25C°) ambient temperatures. With a view to understanding molecular mechanisms we profiled aestivating versus control gastrocnemius muscle using mRNA sequencing. This indicated an extensive metabolic reprogramming, with nearly a quarter of the entire transcriptome (3996 of 16,960 mRNA) exhibiting a nominal >2-fold change. Consistent with a physiological adaptation to spare carbohydrate reserves, carbohydrate catabolism was systemically downregulated. A 630-fold downregulation of ENO3 encoding the enolase enzyme was most striking. The 590 frog orthologs of mRNA encoding the mitoproteome were, viewed as a population, significantly downregulated during aestivation, although not to the same extent as mRNA encoding carbohydrate catabolism. Prominent examples include members of the TCA cycle (IDH2), electron transport chain (NDUFA6), the ATP synthase complex (ATP5F1B) and ADP/ATP intracellular transport (SLC25A4). Moreover, mRNA derived from the mt genome itself (e.g. mt-ND1) were also downregulated. Most prominent among the upregulated mRNA are those encoding aspects of regulated proteolysis including the proteosome (e.g. PSME4L), peptidases (USP25), atrogins (FBXO32) and ubiquitination (VCP). Finally, we note the ∼5-fold upregulation of the mRNA EIFG3 that encodes part of the EIF4F complex. This possesses global control of protein synthesis. Given protein synthesis is repressed in aestivating frogs this indicates the skeletal musculature is poised for accelerated translation of mRNA upon emergence, supporting a strategy to rapidly restore function when the summer rains come.

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低代谢肌肉中 mRNA 在全基因组范围内的剧烈重编程。
为了应对季节性干旱,绿条穴蛙(Cyclorana alboguttata)会进入一种可逆的低代谢状态,这种状态被称为 "休眠"(estivation),在这种状态下,尽管环境温度较高(>25℃),心率和耗氧量也会降低。为了了解分子机制,我们使用 mRNA 测序分析了动情期与对照期的腓肠肌。结果表明,整个转录组(16,960 个 mRNA 中的 3996 个)中有近四分之一发生了名义上大于 2 倍的变化。与为节省碳水化合物储备而进行的生理适应相一致,碳水化合物分解代谢受到了系统性的下调。最引人注目的是编码烯醇化酶的 ENO3 下调了 630 倍。编码有丝分裂蛋白体的 590 个蛙类 mRNA 的同源物作为一个群体,在休眠期受到显著下调,尽管下调程度不如编码碳水化合物分解代谢的 mRNA。突出的例子包括TCA循环(IDH2)、电子传递链(NDUFA6)、ATP合成酶复合物(ATP5F1B)和ADP/ATP胞内转运(SLC25A4)的成员。此外,源自 mt 基因组本身的 mRNA(如 mt-ND1)也出现了下调。在上调的 mRNA 中,最突出的是那些编码蛋白酶体(如 PSME4L)、肽酶(USP25)、atrogins(FBXO32)和泛素化(VCP)等调节蛋白酶解的 mRNA。最后,我们注意到编码 EIF4F 复合物一部分的 mRNA EIFG3 上调了约 5 倍。这就拥有了对蛋白质合成的全面控制。鉴于动情蛙的蛋白质合成受到抑制,这表明骨骼肌在萌发时已准备好加速 mRNA 的翻译,从而支持一种在夏雨到来时迅速恢复功能的策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Accounts of Chemical Research
Accounts of Chemical Research 化学-化学综合
CiteScore
31.40
自引率
1.10%
发文量
312
审稿时长
2 months
期刊介绍: Accounts of Chemical Research presents short, concise and critical articles offering easy-to-read overviews of basic research and applications in all areas of chemistry and biochemistry. These short reviews focus on research from the author’s own laboratory and are designed to teach the reader about a research project. In addition, Accounts of Chemical Research publishes commentaries that give an informed opinion on a current research problem. Special Issues online are devoted to a single topic of unusual activity and significance. Accounts of Chemical Research replaces the traditional article abstract with an article "Conspectus." These entries synopsize the research affording the reader a closer look at the content and significance of an article. Through this provision of a more detailed description of the article contents, the Conspectus enhances the article's discoverability by search engines and the exposure for the research.
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