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首页> 外文期刊>Molecular & cellular proteomics: MCP >On Marathons and Sprints: An Integrated Quantitative Proteomics and Transcriptomics Analysis of Differences Between Slow and Fast Muscle Fibers
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On Marathons and Sprints: An Integrated Quantitative Proteomics and Transcriptomics Analysis of Differences Between Slow and Fast Muscle Fibers

机译:关于马拉松和短跑:慢速和快肌纤维之间差异的定量蛋白质组学和转录组学综合分析

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摘要

Skeletal muscle tissue contains slow as well as fast twitch muscle fibers that possess different metabolic and contractile properties. Although the distribution of individual proteins in fast and slow fibers has been investigated extensively, a comprehensive proteomic analysis, which is key for any systems biology approach to muscle tissues, is missing. Here, we compared the global protein levels and gene expression profiles of the predominantly slow soleus and fast extensor digitorum longus muscles using the principle of in vivo stable isotope labeling with amino acids based on a fully ly-sine-6 labeled SILAC-mouse. We identified 551 proteins with significant quantitative differences between slow soleus and fast extensor digitorum longus fibers out of >2000 quantified proteins, which greatly extends the repertoire of proteins differentially regulated between both muscle types. Most of the differentially regulated proteins mediate cellular contraction, ion homeostasis, glycolysis, and oxidation, which reflect the major functional differences between both muscle types. Comparison of proteomics and transcriptomics data uncovered the existence of fiber-type specific posttranscriptional regulatory mechanisms resulting in differential accumulation of Myosin-8 and alpha-protein kinase 3 proteins and mRNAs among others. Phosphoproteome analysis of soleus and extensor digitorum longus muscles identified 2573 phosphosites on 973 proteins including 1040 novel phosphosites. The in vivo stable isotope labeling with amino acids-mouse approach used in our study provides a comprehensive view into the protein networks that direct fiber-type specific functions and allows a detailed dissection of the molecular composition of slow and fast muscle tissues with unprecedented resolution.
机译:骨骼肌组织包含具有不同代谢和收缩特性的慢肌和快肌。尽管已经广泛研究了快速和慢速纤维中单个蛋白质的分布,但是缺少对任何针对肌肉组织的系统生物学方法都至关重要的综合蛋白质组学分析。在这里,我们使用基于完全由ly-sine-6标记的SILAC小鼠进行体内稳定同位素标记的氨基酸的原理,比较了主要由比目鱼肌和快速指趾长肌慢肌构成的整体蛋白质水平和基因表达谱。我们从超过2000种定量蛋白质中鉴定出551种蛋白质,这些蛋白质在慢比目鱼肌和快速指外趾长肌之间有显着的定量差异,这极大地扩展了两种肌肉类型之间差异调节的蛋白质库。大多数差异调节蛋白介导细胞收缩,离子稳态,糖酵解和氧化,这反映了两种肌肉类型之间的主要功能差异。蛋白质组学和转录组学数据的比较揭示了纤维类型特异性转录后调控机制的存在,这种机制导致Myosin-8和α-蛋白激酶3蛋白和mRNA的差异积累。比目鱼肌和指趾长肌的磷酸化蛋白质组学分析鉴定了973蛋白上的2573个磷酸化位点,其中包括1040个新的磷酸化位点。在我们的研究中使用氨基酸-小鼠方法在体内进行稳定同位素标记,可提供对指导纤维型特定功能的蛋白质网络的全面了解,并能够以前所未有的分辨率详细解剖慢,快肌组织的分子组成。

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