On Marathons and Sprints: An Integrated Quantitative Proteomics and Transcriptomics Analysis of Differences Between Slow and Fast Muscle Fibers

被引:76
作者
Drexler, Hannes C. A. [2 ]
Ruhs, Aaron [1 ]
Konzer, Anne [1 ]
Mendler, Luca [3 ]
Bruckskotten, Mark [1 ]
Looso, Mario [1 ]
Guenther, Stefan [1 ]
Boettger, Thomas [1 ]
Krueger, Marcus [1 ]
Braun, Thomas [1 ]
机构
[1] Max Planck Inst Heart & Lung Res, D-61231 Bad Nauheim, Germany
[2] Max Planck Inst Mol Biomed, D-48149 Munster, Germany
[3] Univ Szeged, Inst Biochem, H-6720 Szeged, Hungary
关键词
DIGITORUM LONGUS MUSCLES; RAT SKELETAL-MUSCLE; GENE-EXPRESSION; M-BAND; BIOMECHANICAL PROPERTIES; EXTRAOCULAR-MUSCLE; SIGNALING NETWORKS; STRIATED-MUSCLE; MYOSIN ISOFORMS; PROTEIN;
D O I
10.1074/mcp.M111.010801
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
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 lysine-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. Molecular & Cellular Proteomics 11: 10.1074/mcp.M111.010801, 1-16, 2012.
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页数:16
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