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      Titin‐based mechanosensing modulates muscle hypertrophy

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          Abstract

          Background

          Titin is an elastic sarcomeric filament that has been proposed to play a key role in mechanosensing and trophicity of muscle. However, evidence for this proposal is scarce due to the lack of appropriate experimental models to directly test the role of titin in mechanosensing.

          Methods

          We used unilateral diaphragm denervation (UDD) in mice, an in vivo model in which the denervated hemidiaphragm is passively stretched by the contralateral, innervated hemidiaphragm and hypertrophy rapidly occurs.

          Results

          In wildtype mice, the denervated hemidiaphragm mass increased 48 ± 3% after 6 days of UDD, due to the addition of both sarcomeres in series and in parallel. To test whether titin stiffness modulates the hypertrophy response, RBM20 ΔRRM and Ttn ΔIAjxn mouse models were used, with decreased and increased titin stiffness, respectively. RBM20 ΔRRM mice (reduced stiffness) showed a 20 ± 6% attenuated hypertrophy response, whereas the Ttn ΔIAjxn mice (increased stiffness) showed an 18 ± 8% exaggerated response after UDD. Thus, muscle hypertrophy scales with titin stiffness. Protein expression analysis revealed that titin‐binding proteins implicated previously in muscle trophicity were induced during UDD, MARP1 & 2, FHL1, and MuRF1.

          Conclusions

          Titin functions as a mechanosensor that regulates muscle trophicity.

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          Most cited references48

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          Ethical guidelines for publishing in the journal of cachexia, sarcopenia and muscle: update 2017

          Abstract This article details an updated version of the principles of ethical authorship and publishing in the Journal of Cachexia, Sarcopenia and Muscle (JCSM). At the time of submission to JCSM, the corresponding author, on behalf of all co‐authors, needs to certify adherence to these principles. The principles are as follows: All authors listed on a manuscript considered for publication have approved its submission and (if accepted) publication as provided to JCSM. No person who has a right to be recognized as author has been omitted from the list of authors on the submitted manuscript. Each author has made a material and independent contribution to the work submitted for publication. The submitted work is original and is neither under consideration elsewhere nor that it has been published previously in whole or in part other than in abstract form. All authors certify that the work is original and does not contain excessive overlap with prior or contemporaneous publication elsewhere, and where the publication reports on cohorts, trials, or data that have been reported on before these other publications must be referenced. All original research work has been approved by the relevant bodies such as institutional review boards or ethics committees. All conflicts of interest, financial or otherwise, that may affect the authors' ability to present data objectively, and relevant sources of funding have been duly declared in the manuscript. The manuscript in its published form will be maintained on the servers of JCSM as a valid publication only as long as all statements in the guidelines on ethical publishing remain true. If any of the aforementioned statements ceases to be true, the authors have a duty to notify the Editors of JCSM as soon as possible so that the available information regarding the published article can be updated and/or the manuscript can be withdrawn.
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            Calcium-dependent molecular spring elements in the giant protein titin.

            Titin (also known as connectin) is a giant protein with a wide range of cellular functions, including providing muscle cells with elasticity. Its physiological extension is largely derived from the PEVK segment, rich in proline (P), glutamate (E), valine (V), and lysine (K) residues. We studied recombinant PEVK molecules containing the two conserved elements: approximately 28-residue PEVK repeats and E-rich motifs. Single molecule experiments revealed that calcium-induced conformational changes reduce the bending rigidity of the PEVK fragments, and site-directed mutagenesis identified four glutamate residues in the E-rich motif that was studied (exon 129), as critical for this process. Experiments with muscle fibers showed that titin-based tension is calcium responsive. We propose that the PEVK segment contains E-rich motifs that render titin a calcium-dependent molecular spring that adapts to the physiological state of the cell.
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              RNA-binding protein RBM20 represses splicing to orchestrate cardiac pre-mRNA processing.

              Mutations in the gene encoding the RNA-binding protein RBM20 have been implicated in dilated cardiomyopathy (DCM), a major cause of chronic heart failure, presumably through altering cardiac RNA splicing. Here, we combined transcriptome-wide crosslinking immunoprecipitation (CLIP-seq), RNA-seq, and quantitative proteomics in cell culture and rat and human hearts to examine how RBM20 regulates alternative splicing in the heart. Our analyses revealed the presence of a distinct RBM20 RNA-recognition element that is predominantly found within intronic binding sites and linked to repression of exon splicing with RBM20 binding near 3' and 5' splice sites. Proteomic analysis determined that RBM20 interacts with both U1 and U2 small nuclear ribonucleic particles (snRNPs) and suggested that RBM20-dependent splicing repression occurs through spliceosome stalling at complex A. Direct RBM20 targets included several genes previously shown to be involved in DCM as well as genes not typically associated with this disease. In failing human hearts, reduced expression of RBM20 affected alternative splicing of several direct targets, indicating that differences in RBM20 expression may affect cardiac function. Together, these findings identify RBM20-regulated targets and provide insight into the pathogenesis of human heart failure.
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                Author and article information

                Contributors
                coeno@email.arizona.edu
                Journal
                J Cachexia Sarcopenia Muscle
                J Cachexia Sarcopenia Muscle
                10.1007/13539.2190-6009
                JCSM
                Journal of Cachexia, Sarcopenia and Muscle
                John Wiley and Sons Inc. (Hoboken )
                2190-5991
                2190-6009
                05 July 2018
                October 2018
                : 9
                : 5 ( doiID: 10.1002/jcsm.v9.5 )
                : 947-961
                Affiliations
                [ 1 ] Department of Cellular and Molecular Medicine University of Arizona Tucson AZ USA
                [ 2 ] Dept of Physiology VU University Medical Center Amsterdam The Netherlands
                [ 3 ] Department of Integrative Pathophysiology Medical Faculty Mannheim Mannheim Germany
                [ 4 ] Myomedix GmbH Neckargemuend Germany
                Author notes
                [*] [* ] Correspondence to: Coen A.C. Ottenheijm, Cellular and Molecular Medicine, University of Arizona, Tucson, AZ, USA. Phone: 520‐626‐4198, Email: coeno@ 123456email.arizona.edu
                Article
                JCSM12319 JCSM-D-18-00008
                10.1002/jcsm.12319
                6204599
                29978560
                c130876e-fbe7-4402-93ba-c67ff512d337
                © 2018 The Authors. Journal of Cachexia, Sarcopenia and Muscle published by John Wiley & Sons Ltd on behalf of the Society on Sarcopenia, Cachexia and Wasting Disorders

                This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.

                History
                : 08 January 2018
                : 30 April 2018
                : 22 May 2018
                Page count
                Figures: 7, Tables: 0, Pages: 15, Words: 7209
                Funding
                Funded by: Foundation Leducq
                Award ID: 13CVD04
                Funded by: MSCA‐RISE‐2014
                Award ID: 645648
                Funded by: National Institutes of Health
                Award ID: R01HL121500
                Categories
                Original Article
                Original Articles
                Custom metadata
                2.0
                jcsm12319
                October 2018
                Converter:WILEY_ML3GV2_TO_NLMPMC version:version=5.5.1 mode:remove_FC converted:29.10.2018

                Orthopedics
                diaphragm,denervation,muscle stretch,hypertrophy,titin,mechanosensing
                Orthopedics
                diaphragm, denervation, muscle stretch, hypertrophy, titin, mechanosensing

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