Literature DB >> 21148390

Nebulin and N-WASP cooperate to cause IGF-1-induced sarcomeric actin filament formation.

Kazunori Takano1, Haruko Watanabe-Takano, Shiro Suetsugu, Souichi Kurita, Kazuya Tsujita, Sumiko Kimura, Takashi Karatsu, Tadaomi Takenawa, Takeshi Endo.   

Abstract

Insulin-like growth factor 1 (IGF-1) induces skeletal muscle maturation and enlargement (hypertrophy). These responses require protein synthesis and myofibril formation (myofibrillogenesis). However, the signaling mechanisms of myofibrillogenesis remain obscure. We found that IGF-1-induced phosphatidylinositol 3-kinase-Akt signaling formed a complex of nebulin and N-WASP at the Z bands of myofibrils by interfering with glycogen synthase kinase-3β in mice. Although N-WASP is known to be an activator of the Arp2/3 complex to form branched actin filaments, the nebulin-N-WASP complex caused actin nucleation for unbranched actin filament formation from the Z bands without the Arp2/3 complex. Furthermore, N-WASP was required for IGF-1-induced muscle hypertrophy. These findings present the mechanisms of IGF-1-induced actin filament formation in myofibrillogenesis required for muscle maturation and hypertrophy and a mechanism of actin nucleation.

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Year:  2010        PMID: 21148390     DOI: 10.1126/science.1197767

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  44 in total

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10.  Deleting nebulin's C-terminus reveals its importance to sarcomeric structure and function and is sufficient to invoke nemaline myopathy.

Authors:  Frank Li; Elisabeth R Barton; Henk Granzier
Journal:  Hum Mol Genet       Date:  2019-05-15       Impact factor: 6.150

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