Search engine for discovering works of Art, research articles, and books related to Art and Culture
ShareThis
Javascript must be enabled to continue!

Nuclear alignment in myotubes requires centrosome proteins recruited by nesprin-1

View through CrossRef
ABSTRACT Myotubes are syncytial cells generated by fusion of myoblasts. Among the numerous nuclei in myotubes of skeletal muscle fibres, the majority are equidistantly positioned at the periphery, except for clusters of multiple nuclei underneath the motor endplate. The correct positioning of nuclei is thought to be important for muscle function and requires nesprin-1 (also known as SYNE1), a protein of the nuclear envelope. Consistent with this, mice lacking functional nesprin-1 show defective nuclear positioning and present aspects of Emery–Dreifuss muscular dystrophy. In this study, we perform small interfering RNA (siRNA) experiments in C2C12 myoblasts undergoing differentiation, demonstrating that the positioning of nuclei requires PCM-1, a protein of the centrosome that relocalizes to the nuclear envelope at the onset of differentiation in a manner that is dependent on the presence of nesprin-1. PCM-1 itself is required for recruiting proteins of the dynein–dynactin complex and of kinesin motor complexes. This suggests that microtubule motors that are attached to the nuclear envelope support the movement of nuclei along microtubules, to ensure their correct positioning in the myotube.
Title: Nuclear alignment in myotubes requires centrosome proteins recruited by nesprin-1
Description:
ABSTRACT Myotubes are syncytial cells generated by fusion of myoblasts.
Among the numerous nuclei in myotubes of skeletal muscle fibres, the majority are equidistantly positioned at the periphery, except for clusters of multiple nuclei underneath the motor endplate.
The correct positioning of nuclei is thought to be important for muscle function and requires nesprin-1 (also known as SYNE1), a protein of the nuclear envelope.
Consistent with this, mice lacking functional nesprin-1 show defective nuclear positioning and present aspects of Emery–Dreifuss muscular dystrophy.
In this study, we perform small interfering RNA (siRNA) experiments in C2C12 myoblasts undergoing differentiation, demonstrating that the positioning of nuclei requires PCM-1, a protein of the centrosome that relocalizes to the nuclear envelope at the onset of differentiation in a manner that is dependent on the presence of nesprin-1.
PCM-1 itself is required for recruiting proteins of the dynein–dynactin complex and of kinesin motor complexes.
This suggests that microtubule motors that are attached to the nuclear envelope support the movement of nuclei along microtubules, to ensure their correct positioning in the myotube.

Related Results

Optogenetic induction of contractile ability in immature C2C12 myotubes
Optogenetic induction of contractile ability in immature C2C12 myotubes
AbstractMyoblasts can be differentiated into multinucleated myotubes, which provide a well-established and reproducible muscle cell model for skeletal myogenesis in vitro. However,...
Catalytic growth in a shared enzyme pool ensures robust control of centrosome size
Catalytic growth in a shared enzyme pool ensures robust control of centrosome size
Abstract Accurate regulation of centrosome size is essential for ensuring error-free cell division, and dysregulation of centrosome size has been linked to various pathologies, inc...
Catalytic growth in a shared enzyme pool ensures robust control of centrosome size
Catalytic growth in a shared enzyme pool ensures robust control of centrosome size
Accurate regulation of centrosome size is essential for ensuring error-free cell division, and dysregulation of centrosome size has been linked to various pathologies, including de...
Centrosome centering and Decentering by microtubule network rearrangement
Centrosome centering and Decentering by microtubule network rearrangement
AbstractThe centrosome is positioned at the cell center by pushing and pulling forces transmitted by microtubules (MTs). Centrosome decentering is often considered to result from a...
HERG1 Expression Increases Calpain Activity in C2C12 Myotubes
HERG1 Expression Increases Calpain Activity in C2C12 Myotubes
Skeletal muscle atrophy is the loss of muscle size and strength caused by an imbalance in protein degradation and protein synthesis. It occurs with normal aging, neural and skeleta...
Spatial and mechanical environments regulate the heterogeneity of myonuclei
Spatial and mechanical environments regulate the heterogeneity of myonuclei
AbstractSkeletal muscle formation involves tight interactions between muscle cells and associated connective tissue fibroblasts. Every muscle displays the same type of organisation...
Abstract 453: The role of centrosome amplification in HCC
Abstract 453: The role of centrosome amplification in HCC
Abstract Centrosome is the major microtubule organizing center (MTOC) in mammalian cells which maintain cell polarity, organization of microtubules and regulate cell...
Caspar modulates primordial germ cell fate both in an Oskar-dependent and Oskar-independent manner
Caspar modulates primordial germ cell fate both in an Oskar-dependent and Oskar-independent manner
ABSTRACT Primordial germ cell (PGC) formation and specification is a fundamental conserved process as PGCs are the progenitors of germline stem cells (GSCs). In Dros...

Back to Top