Nebulin-deficient mice exhibit shorter thin filament lengths and reduced contractile function in skeletal muscle

Nebulin is a giant modular sarcomeric protein that has been proposed to play critical roles in myofibrillogenesis, thin filament length regulation, and muscle contraction. To investigate the functional role of nebulin in vivo, we generated nebulin-deficient mice by using a Cre knock-in strategy. Lineage studies utilizing this mouse model demonstrated that nebulin is expressed uniformly in all skeletal muscles. Nebulin-deficient mice die within 8–11 d after birth, with symptoms including decreased milk intake and muscle weakness. Although myofibrillogenesis had occurred, skeletal muscle thin filament lengths were up to 25% shorter compared with wild type, and thin filaments were uniform in length both within and between muscle types. Ultrastructural studies also demonstrated a critical role for nebulin in the maintenance of sarcomeric structure in skeletal muscle. The functional importance of nebulin in skeletal muscle function was revealed by isometric contractility assays, which demonstrated a dramatic reduction in force production in nebulin-deficient skeletal muscle.

[1]  A. Chapelle,et al.  Clinical and genetic heterogeneity in autosomal recessive nemaline myopathy , 1999, Neuromuscular Disorders.

[2]  D. Root,et al.  Calmodulin-sensitive interaction of human nebulin fragments with actin and myosin. , 1994, Biochemistry.

[3]  C. Gregorio,et al.  Nebulin regulates the assembly and lengths of the thin filaments in striated muscle , 2005, The Journal of cell biology.

[4]  M. Bang,et al.  Molecular dissection of the interaction of desmin with the C-terminal region of nebulin. , 2002, Journal of structural biology.

[5]  C. Moncman,et al.  Nebulette: a 107 kD nebulin-like protein in cardiac muscle. , 1995, Cell motility and the cytoskeleton.

[6]  Kuan Wang,et al.  Interaction of nebulin SH3 domain with titin PEVK and myopalladin: implications for the signaling and assembly role of titin and nebulin , 2002, FEBS letters.

[7]  C. Gregorio,et al.  The N-terminal End of Nebulin Interacts with Tropomodulin at the Pointed Ends of the Thin Filaments* , 2001, The Journal of Biological Chemistry.

[8]  H. Hinssen,et al.  Identification and localisation of nebulin as a thin filament component of invertebrate chordate muscles , 1999, Journal of Comparative Physiology B.

[9]  K. Pelin,et al.  Complete genomic structure of the human nebulin gene and identification of alternatively spliced transcripts , 2004, European Journal of Human Genetics.

[10]  H. Hinssen,et al.  Nebulin is a thin filament protein of the cardiac muscle of the agnathans , 2004, Journal of Muscle Research & Cell Motility.

[11]  J. Lin,et al.  Erythrocyte tropomodulin binds to the N-terminus of hTM5, a tropomyosin isoform encoded by the gamma-tropomyosin gene. , 1994, Biochemical and biophysical research communications.

[12]  J. Ross,et al.  Selective Requirement of Myosin Light Chain 2v in Embryonic Heart Function* , 1998, The Journal of Biological Chemistry.

[13]  Y. Shimada,et al.  Relation of nebulin and connectin (titin) to dynamics of actin in nascent myofibrils of cultured skeletal muscle cells. , 1999, Experimental cell research.

[14]  R. Horowits Nebulin regulation of actin filament lengths: new angles. , 2006, Trends in cell biology.

[15]  R L Lieber,et al.  Desmin knockout muscles generate lower stress and are less vulnerable to injury compared with wild-type muscles. , 2000, American journal of physiology. Cell physiology.

[16]  C. Gregorio,et al.  Nebulin: the nebulous, multifunctional giant of striated muscle. , 2003, Trends in cardiovascular medicine.

[17]  G. Butler-Browne,et al.  Myosin heavy chain isoforms in postnatal muscle development of mice , 2003, Biology of the cell.

[18]  R. Lieber,et al.  Relationship between muscle fiber types and sizes and muscle architectural properties in the mouse hindlimb , 1994, Journal of morphology.

[19]  K. Pelin,et al.  Mutations in the nebulin gene can cause severe congenital nemaline myopathy , 2002, Neuromuscular Disorders.

[20]  H. T. ter Keurs,et al.  Effect of thin filament length on the force-sarcomere length relation of skeletal muscle. , 1991, The American journal of physiology.

[21]  V. Fowler,et al.  Defining actin filament length in striated muscle: rulers and caps or dynamic stability? , 1998, Annual review of cell and developmental biology.

[22]  S J Winder,et al.  Nebulin, a helical actin binding protein. , 1994, The EMBO journal.

[23]  K. Wang,et al.  Architecture of the sarcomere matrix of skeletal muscle: immunoelectron microscopic evidence that suggests a set of parallel inextensible nebulin filaments anchored at the Z line , 1988, The Journal of cell biology.

[24]  V. Fowler,et al.  Nebulin: Does It Measure up as a Ruler? , 2006, Current Biology.

[25]  A. Huxley,et al.  Proposed Mechanism of Force Generation in Striated Muscle , 1971, Nature.

[26]  K. Wang Titin/connectin and nebulin: giant protein rulers of muscle structure and function. , 1996, Advances in biophysics.

[27]  C. Moncman,et al.  Assembly of nebulin into the sarcomeres of avian skeletal muscle. , 1996, Cell motility and the cytoskeleton.

[28]  M. Bang,et al.  Myopalladin, a Novel 145-Kilodalton Sarcomeric Protein with Multiple Roles in Z-Disc and I-Band Protein Assemblies , 2001, The Journal of cell biology.

[29]  Siegfried Labeit,et al.  Titins: Giant Proteins in Charge of Muscle Ultrastructure and Elasticity , 1995, Science.

[30]  Christian C Witt,et al.  The complete mouse nebulin gene sequence and the identification of cardiac nebulin. , 2003, Journal of molecular biology.

[31]  D. Morgan,et al.  Early events in stretch-induced muscle damage. , 1999, Journal of applied physiology.

[32]  Philippe Soriano Generalized lacZ expression with the ROSA26 Cre reporter strain , 1999, Nature Genetics.

[33]  V. Fowler,et al.  Measurement of thin filament lengths by distributed deconvolution analysis of fluorescence images. , 2002, Biophysical journal.

[34]  J. Fridén,et al.  Functional and clinical significance of skeletal muscle architecture , 2000, Muscle & nerve.

[35]  Velia M. Fowler,et al.  Actin dynamics at pointed ends regulates thin filament length in striated muscle , 2001, Nature Cell Biology.

[36]  K. Pelin,et al.  Characterization of nebulette and nebulin and emerging concepts of their roles for vertebrate Z-discs. , 1998, Journal of molecular biology.

[37]  J. Chrast,et al.  Comparison of contraction and calcium handling between right and left ventricular myocytes from adult mouse heart: a role for repolarization waveform , 2006, The Journal of physiology.

[38]  S. Begum,et al.  Development of connectin/titin and nebulin in striated muscles of chicken. , 1996, Advances in biophysics.

[39]  Kuan Wang,et al.  Nebulin as a giant actin‐binding template protein in skeletal muscle sarcomere Interaction of actin and cloned human nebulin fragments , 1991, FEBS letters.

[40]  D. Root,et al.  High-affinity actin-binding nebulin fragments influence the actoS1 complex. , 2001, Biochemistry.

[41]  A. Huxley,et al.  The variation in isometric tension with sarcomere length in vertebrate muscle fibres , 1966, The Journal of physiology.

[42]  So-young Kim,et al.  Identification of chicken nebulin isoforms of the 31-residue motifs and non-muscle nebulin. , 2004, Biochemical and biophysical research communications.