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Keywords: Myogenesis
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Journal Articles
J Cell Sci (2022) 135 (1): jcs259097.
Published: 12 January 2022
... with transforming growth factor-β (TGF-β)–Smad and Wnt/β-catenin pathways. Previously, we implicated Smad7 and β-catenin in mammalian myogenesis. Therefore, we assessed a potential role of TAZ on the Smad7–β-catenin complex in muscle cells. Here, we document functional interactions between Smad7, TAZ and β-catenin...
Includes: Supplementary data
Journal Articles
J Cell Sci (2022) 135 (5): jcs258649.
Published: 19 October 2021
... Ltd 2022 Summary: Myoblasts exhibit an aminophospholipid flippase activity that relies on CDC50A-dependent P4-ATPases. Loss of CDC50A compromises actin remodeling, RAC1 membrane targeting and cell fusion. Phospholipid Aminophospholipid translocase P4-ATPase Myogenesis Skeletal...
Includes: Supplementary data
Journal Articles
J Cell Sci (2020) 133 (8): jcs240325.
Published: 28 April 2020
...Yen-Ling Lian; Kuan-Wei Chen; Yu-Ting Chou; Ting-Ling Ke; Bi-Chang Chen; Yu-Chun Lin; Linyi Chen ABSTRACT Myoblast fusion is required for myotube formation during myogenesis, and defects in myoblast differentiation and fusion have been implicated in a number of diseases, including human...
Includes: Supplementary data
Journal Articles
J Cell Sci (2017) 130 (21): 3685–3697.
Published: 01 November 2017
... with, those of the muscle stem cell master regulator, Pax7. Facioscapulohumeral muscular dystrophy DUX4 Myogenesis Homeodomain Pax3 Pax7 Facioscapulohumeral muscular dystrophy (FSHD) is a dominant inherited myopathy caused by mutations that lead to loss of repeat-induced silencing...
Includes: Supplementary data
Journal Articles
J Cell Sci (2017) 130 (5): 950–962.
Published: 01 March 2017
.... ( 1998 ). inscuteable and numb mediate asymmetric muscle progenitor cell divisions during Drosophila myogenesis . Genes Dev.   12 , 304 - 315 . 10.1101/gad.12.3.304 Chanana , B. , Graf , R. , Koledachkina , T. , Pflanz , R. and Vorbrüggen , G. ( 2007 ). AlphaPS2 integrin...
Includes: Supplementary data
Journal Articles
J Cell Sci (2016) 129 (22): 4305–4316.
Published: 15 November 2016
...Xingyu Zhou; Mingsen Li; Huaxing Huang; Keren Chen; Zhuning Yuan; Ying Zhang; Yaping Nie; Hu Chen,; Xumeng Zhang; Luxi Chen; Yaosheng Chen; Delin Mo ABSTRACT Although the mechanism underlying modulation of transcription factors in myogenesis has been well elucidated, the function...
Includes: Supplementary data
Journal Articles
J Cell Sci (2016) 129 (21): 4076–4090.
Published: 01 November 2016
...Stephanie Wales Tobin; Dabo Yang; John Girgis; Ali Farahzad; Alexandre Blais; John C. McDermott ABSTRACT Mycocyte enhancer factor 2 (MEF2) and activator protein 1 (AP-1) transcription complexes have been individually implicated in myogenesis, but their genetic interaction has not previously been...
Includes: Supplementary data
Journal Articles
J Cell Sci (2016) 129 (18): 3426–3436.
Published: 15 September 2016
... protein Kette is essential for myoblast fusion. It controls the dissolution of electron-dense plaques and the ratio of Scar and WASp proteins in fusion-competent myoblasts during fusion pore formation. Myogenesis Myoblast fusion WAVE F-actin Wip Vrp1 Cellular junction Myoblast fusion...
Includes: Supplementary data
Journal Articles
J Cell Sci (2016) 129 (15): 2887–2896.
Published: 01 August 2016
... development, myoblasts and satellite cell proliferation and differentiation in vertebrates. We also outline the relationship between Notch, Wnt and growth factor signalling pathways, as well as the post-transcriptional regulation of myogenesis under conditions of hypoxia. * Authors for correspondence...
Journal Articles
J Cell Sci (2016) 129 (14): 2767–2777.
Published: 15 July 2016
...Yan Huang; Bohong Chen; Miaoman Ye; Puping Liang; Yingnan Zhangfang; Junjiu Huang; Mingyao Liu; Zhou Songyang; Wenbin Ma ABSTRACT Skeletal myogenesis is a multistep process in which basic helix-loop-helix (bHLH) transcription factors, such as MyoD (also known as MyoD1), bind to E-boxes and activate...
Includes: Supplementary data
Journal Articles
J Cell Sci (2015) 128 (19): 3631–3645.
Published: 01 October 2015
...Demetris Koutalianos; Andrie Koutsoulidou; Nikilaos P. Mastroyiannopoulos; Denis Furling; Leonidas A. Phylactou ABSTRACT Twist-1 is mostly expressed during development and has been previously shown to control myogenesis. Because its regulation in muscle has not been fully exploited, the aim...
Includes: Supplementary data
Journal Articles
J Cell Sci (2015) 128 (9): 1707–1717.
Published: 01 May 2015
... that Bit‐1 controls skeletal myogenesis through a caspase‐mediated signaling pathway. Bit‐1 ‐null mice exhibit a myopathy with hypotrophic myofibers. Bit‐1 ‐null myoblasts prematurely express muscle‐specific proteins. Similarly, knockdown of Bit‐1 expression in C2C12 myoblasts promotes early...
Journal Articles
J Cell Sci (2014) 127 (21): 4634–4644.
Published: 01 November 2014
... 1 ). To test their function in adult myogenesis, a morphogenetic process where Notch signalling is implicated in both cell fate and cell migration ( Anant et al., 1998 ; Gildor et al., 2012 ), expression of hairpin RNAs targeting the individual genes was directed to the AMPs (using 1151-Gal4...
Includes: Supplementary data
Journal Articles
J Cell Sci (2014) 127 (15): 3240–3256.
Published: 01 August 2014
.... Muscle regeneration Myogenesis Matn2 shRNA TGF-β signaling BMP signaling NFI Trf3 Skeletal muscle regeneration following injury is a multistep process that restores the tissue architecture by the sequential activation of multiple signaling pathways ( Chargé and Rudnicki, 2004 ; Wagers...
Includes: Supplementary data
Journal Articles
J Cell Sci (2014) 127 (14): 3162–3173.
Published: 15 July 2014
...) in myofibrillogenesis. Expression of perd RNAi in muscles, prior to adult myogenesis, can induce misorientation and detachment of Drosophila adult abdominal muscles. In comparison to controls, perd -depleted muscles contain fewer myofibrils, which are localized at the cell periphery. These myofibrils are detached from...
Includes: Supplementary data
Journal Articles
J Cell Sci (2014) 127 (10): 2291–2301.
Published: 15 May 2014
...Jenean H. O'Brien; Laura Hernandez-Lagunas; Kristin Bruk Artinger; Heide L. Ford ABSTRACT Precise spatiotemporal regulation of the SIX1 homeoprotein is required to coordinate vital tissue development, including myogenesis. Whereas SIX1 is downregulated in most tissues following embryogenesis...
Includes: Supplementary data
Journal Articles
J Cell Sci (2013) 126 (22): 5116–5131.
Published: 15 November 2013
... © 2013. Published by The Company of Biologists Ltd 2013 Satellite cells Cell division Dystrophin M-cadherin Myogenesis Muscle is one of the few tissues composed of cells with various nuclei. Based on transmitted electron microscope observations, initially it was postulated...
Includes: Supplementary data
Journal Articles
J Cell Sci (2013) 126 (11): 2525–2533.
Published: 01 June 2013
...Fabrice Antigny; Stéphane Koenig; Laurent Bernheim; Maud Frieden Summary Myogenesis involves expression of muscle-specific transcription factors such as myogenin and myocyte enhancer factor 2 (MEF2), and is essentially regulated by fluctuations of cytosolic Ca 2+ concentration. Recently we...
Includes: Supplementary data
Journal Articles
J Cell Sci (2013) 126 (10): 2213–2224.
Published: 15 May 2013
... 1 (Bmal1), an essential transcriptional activator of the clock, is highly expressed in skeletal muscle. However, whether this key clock component impacts myogenesis, a temporally regulated event that requires the sequential activation of myogenic regulatory factors, is not known. Here we report...
Includes: Supplementary data
Journal Articles
J Cell Sci (2013) 126 (8): 1868–1880.
Published: 15 April 2013
... at desired stage in 4% PFA over night, dehydrated in 100% methanol and stored at −20°C until analysis using immunohistochemistry. Transforming growth factor beta (Tgfβ) signalling, including bone morphogenetic proteins (BMPs) can act on myogenesis through phosphorylated Smad ( Yamamoto et al., 1997...
Includes: Supplementary data