| First Author | Seto JT | Year | 2011 |
| Journal | Hum Mol Genet | Volume | 20 |
| Issue | 15 | Pages | 2914-27 |
| PubMed ID | 21536590 | Mgi Jnum | J:173409 |
| Mgi Id | MGI:5014004 | Doi | 10.1093/hmg/ddr196 |
| Citation | Seto JT, et al. (2011) Deficiency of {alpha}-actinin-3 is associated with increased susceptibility to contraction-induced damage and skeletal muscle remodeling. Hum Mol Genet 20(15):2914-27 |
| abstractText | Sarcomeric alpha-actinins (alpha-actinin-2 and -3) are a major component of the Z-disk in skeletal muscle, where they crosslink actin and other structural proteins to maintain an ordered myofibrillar array. Homozygosity for the common null polymorphism (R577X) in ACTN3 results in the absence of fast fiber-specific alpha-actinin-3 in approximately 20% of the general population. alpha-Actinin-3 deficiency is associated with decreased force generation and is detrimental to sprint and power performance in elite athletes, suggesting that alpha-actinin-3 is necessary for optimal forceful repetitive muscle contractions. Since Z-disks are the structures most vulnerable to eccentric damage, we sought to examine the effects of alpha-actinin-3 deficiency on sarcomeric integrity. Actn3 knockout mouse muscle showed significantly increased force deficits following eccentric contraction at 30% stretch, suggesting that alpha-actinin-3 deficiency results in an increased susceptibility to muscle damage at the extremes of muscle performance. Microarray analyses demonstrated an increase in muscle remodeling genes, which we confirmed at the protein level. The loss of alpha-actinin-3 and up-regulation of alpha-actinin-2 resulted in no significant changes to the total pool of sarcomeric alpha-actinins, suggesting that alterations in fast fiber Z-disk properties may be related to differences in functional protein interactions between alpha-actinin-2 and alpha-actinin-3. In support of this, we demonstrated that the Z-disk proteins, ZASP, titin and vinculin preferentially bind to alpha-actinin-2. Thus, the loss of alpha-actinin-3 changes the overall protein composition of fast fiber Z-disks and alters their elastic properties, providing a mechanistic explanation for the loss of force generation and increased susceptibility to eccentric damage in alpha-actinin-3-deficient individuals. |
