Titin is a 3000-4000 kD protein found in heart and skeletal muscle, and it has been proposed to play a major role in controlling the resting or passive tension in these tissues. Major developmental changes have been found to occur in cardiac titin as a result of alternative splicing pathways. A unique rat strain has been discovered with an autosomal dominant mutation that leads to a delayed fetal-to-adult titin transition pattern. These animals will be used to test the role of titin in cardiac hemodynamics in the intact animal using echocardiography and pressure-volume relationship measurements. Mechanical experiments on single cardiomyocytes will test hypotheses regarding titin's role in rest tension and the Frank-Starling relationship. Interactions betweer_ positively charged PPAK peptides from titin's extensible PEVK region with negatively charged polyE peptides will be tested using chromatographic, circular dichroism, electrophoretic, and surface plasmon resonance techniques. Studies will be designed to determine if binding of the PPAK and polyE peptides is specific to adjacent regions in the sequence or if multiple types of interactions can occur. Nontitin peptides rich in glutamic acid will also be examined for binding. Previously proposed phosphorylation sites will be identified in expressed titin polypeptides, and these sites will also be assayed for )hosphorylation state in intact fetal and adult titins. These experiments will test the hypothesis that certain _ites must be phosphorylated for proper assembly and/or function. Gene mapping studies will be conducted to localize the mutation site leading to the delayed developmental titin isoform program. The proposed studies will provide new information regarding the structure and function of this giant protein and its relation to human health and cardiovascular disease. The work may also provide novel insights on mechanisms of alternative splicing, an area of increasing importance in understanding the proteome. ? ?

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
1R01HL077196-01
Application #
6808924
Study Section
Cardiac Contractility, Hypertrophy, and Failure Study Section (CCHF)
Program Officer
Schramm, Charlene A
Project Start
2004-07-01
Project End
2008-05-31
Budget Start
2004-07-01
Budget End
2005-05-31
Support Year
1
Fiscal Year
2004
Total Cost
$291,000
Indirect Cost
Name
University of Wisconsin Madison
Department
Veterinary Sciences
Type
Schools of Earth Sciences/Natur
DUNS #
161202122
City
Madison
State
WI
Country
United States
Zip Code
53715
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Greaser, Marion L; Warren, Chad M (2015) Method for resolution and western blotting of very large proteins using agarose electrophoresis. Methods Mol Biol 1312:285-91
Hanft, Laurin M; Greaser, Marion L; McDonald, Kerry S (2014) Titin-mediated control of cardiac myofibrillar function. Arch Biochem Biophys 552-553:83-91
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Li, Shijun; Guo, Wei; Dewey, Colin N et al. (2013) Rbm20 regulates titin alternative splicing as a splicing repressor. Nucleic Acids Res 41:2659-72
Mateja, Ryan D; Greaser, Marion L; de Tombe, Pieter P (2013) Impact of titin isoform on length dependent activation and cross-bridge cycling kinetics in rat skeletal muscle. Biochim Biophys Acta 1833:804-11
Patel, Jitandrakumar R; Pleitner, Jonathan M; Moss, Richard L et al. (2012) Magnitude of length-dependent changes in contractile properties varies with titin isoform in rat ventricles. Am J Physiol Heart Circ Physiol 302:H697-708
Guo, Wei; Schafer, Sebastian; Greaser, Marion L et al. (2012) RBM20, a gene for hereditary cardiomyopathy, regulates titin splicing. Nat Med 18:766-73
Greaser, Marion L; Warren, Chad M (2012) Protein electrophoresis in agarose gels for separating high molecular weight proteins. Methods Mol Biol 869:111-8
Li, Shijun; Guo, Wei; Schmitt, Benjamin M et al. (2012) Comprehensive analysis of titin protein isoform and alternative splicing in normal and mutant rats. J Cell Biochem 113:1265-73

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