In recent years, we have learned a great deal about the assembly of thick and thin filaments in striated muscle, and about the proteins that regulate the release and re-uptake of Ca2+ essential for the contractile cycle. We know much less, however, about the mechanisms that integrate thick and thin filaments into myofibrils, and about the proteins that organize the sarcoplasmic reticulum (SR) and transverse (t-) tubules so regularly around sarcomere. The recent discovery of obscurin offers new ways to address these questions. Obscurin is an approximately 800 kDa protein with structural homology to titin. It is the only protein of the titin superfamily that is concentrated, at least in part, at the periphery of sarcomeres, primarily around M-lines and Z-disks. Obscurin is composed largely of tandem Ig domains but also has signaling domains and, at its extreme COOH-terminus, a binding site for a small, integral membrane form of ankyrin 1 that is concentrated in the network SR. Given its apparent ability to concentrate at the periphery of the myofibril around M-lines and Z-disks and its high affinity for an integral protein of the SR membrane, obscurin is ideally suited to play key roles in assembling and organizing both the sarcomere and the SR. We propose to test this general hypothesis through 4 specific aims: (1) to learn how obscurin is organized with respect to key structures within sarcomeres;(2) to learn how obscurin binds to elements in the contractile apparatus;(3) to assess the effect on morphogenesis of the myofibrils and associated membranes of altering the activity of obscurin with siRNA and thru adenoviral overexpression of particular binding domains;and (4) to investigate the role of obscurin's binding to small ankyrin 1 in the assembly, organization and function of the SR. Mutations in proteins of the contractile apparatus, including some that affect the assembly or stability of contractile elements, have been implicated in hypertrophic cardiomyopathies and muscular dystrophies. The results of our experiments should reveal some of the key mechanisms involved in assembling contractile proteins into sarcomeres and in determining their association with the SR.

National Institute of Health (NIH)
National Heart, Lung, and Blood Institute (NHLBI)
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Special Emphasis Panel (ZRG1-CVS-D (03))
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Adhikari, Bishow B
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University of Maryland Baltimore
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Ackermann, Maegen A; Ziman, Andrew P; Strong, John et al. (2011) Integrity of the network sarcoplasmic reticulum in skeletal muscle requires small ankyrin 1. J Cell Sci 124:3619-30
Ford-Speelman, Diana L; Roche, Joseph A; Bowman, Amber L et al. (2009) The rho-guanine nucleotide exchange factor domain of obscurin activates rhoA signaling in skeletal muscle. Mol Biol Cell 20:3905-17
Ackermann, Maegen A; Hu, Li-Yen R; Bowman, Amber L et al. (2009) Obscurin interacts with a novel isoform of MyBP-C slow at the periphery of the sarcomeric M-band and regulates thick filament assembly. Mol Biol Cell 20:2963-78
Kontrogianni-Konstantopoulos, Aikaterini; Ackermann, Maegen A; Bowman, Amber L et al. (2009) Muscle giants: molecular scaffolds in sarcomerogenesis. Physiol Rev 89:1217-67
Borzok, Maegen A; Catino, Dawn H; Nicholson, James D et al. (2007) Mapping the binding site on small ankyrin 1 for obscurin. J Biol Chem 282:32384-96
Bowman, Amber L; Kontrogianni-Konstantopoulos, Aikaterini; Hirsch, Sara S et al. (2007) Different obscurin isoforms localize to distinct sites at sarcomeres. FEBS Lett 581:1549-54
Kontrogianni-Konstantopoulos, Aikaterini; Catino, Dawn H; Strong, John C et al. (2006) De novo myofibrillogenesis in C2C12 cells: evidence for the independent assembly of M bands and Z disks. Am J Physiol Cell Physiol 290:C626-37
Borisov, Andrei B; Sutter, Sarah B; Kontrogianni-Konstantopoulos, Aikaterini et al. (2006) Essential role of obscurin in cardiac myofibrillogenesis and hypertrophic response: evidence from small interfering RNA-mediated gene silencing. Histochem Cell Biol 125:227-38
Kontrogianni-Konstantopoulos, Aikaterini; Catino, Dawn H; Strong, John C et al. (2006) Obscurin modulates the assembly and organization of sarcomeres and the sarcoplasmic reticulum. FASEB J 20:2102-11
Kontrogianni-Konstantopoulos, Aikaterini; Bloch, Robert J (2005) Obscurin: a multitasking muscle giant. J Muscle Res Cell Motil 26:419-26

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