Titin is an extremely large protein found primarily in cardiac and skeletal muscle. It is alternatively spliced and different splice isoforms affect the function of the protein. We have partially characterized a mutation in rats that dramatically alters the splicing pattern of titin in the heart. The mutated gene responsible for altered titin splicing has been localized to an RNA binding protein in chromosome 1. Transfection of adenovirus constructs contain the Rbm20 sequence into cultured cardiomyocytes from homozygous mutants will be used in rescue experiments. Binding of the Rbm20 to RNA or DNA will be explored using ChIP assays. Alternative mechanisms whereby titin splicing is developmentally changed will be explored. These include developmental up regulation of Rbm20 message and protein using quantitative PCR and Western blotting respectively, developmental alterations in Rbm20 phosphorylation state, or developmental changes in other protein or proteins that associate with Rbm20. The role of titin in stretch dependent signal transduction will be explored using the titin splice mutation model for comparisons with wild type animals after pressure and volume overload challenges. Experiments where the titin stretch signals can be balance using heterozygote mutants and a model system where titin expression is altered by propylthiouricil will be conducted. Changes in gene expression will be measured using quantitative PCR and Western blots. Studies will be conducted to characterize the prolonged duration of action potentials from cardiomyocytes of homozygous mutants and determine whether the altered ion channel properties found in isolated cells are also observed in vivo. We will also use the mutant rat model to explore titin's role in length dependent activation and the Frank-Starling relationship using isolated skinned cardiomyocytes. X- ray diffraction experiments using skinned trabeculae will compare filament spacing of wild type, heterozygote, and homozygote mutants at different sarcomere lengths. The studies outlined should provide new insights into titin function and the mechanisms controlling its isoform expression. They may also help to better understand the role of ion channel alternative splicing on cardiac arrhythmias.

Public Health Relevance

Titin isoforms changes have been shown to occur in dilated cardiomyopathy, so understanding the mechanisms controlling titin splicing and the cardiac adaptations to different titin isoforms may help in devising treatments for this prevalent cardiovascular disease. In addition the rat mutation model we have developed should help to understand mechanisms of cardiac arrhythmia and sudden death.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
5R01HL077196-06
Application #
7851384
Study Section
Cardiac Contractility, Hypertrophy, and Failure Study Section (CCHF)
Program Officer
Schramm, Charlene A
Project Start
2004-07-01
Project End
2012-06-30
Budget Start
2010-07-01
Budget End
2012-06-30
Support Year
6
Fiscal Year
2010
Total Cost
$363,063
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
Ait-Mou, Younss; Zhang, Mengjie; Martin, Jody L et al. (2017) Impact of titin strain on the cardiac slow force response. Prog Biophys Mol Biol 130:281-287
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
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
Guo, Wei; Pleitner, Jonathan M; Saupe, Kurt W et al. (2013) Pathophysiological defects and transcriptional profiling in the RBM20-/- rat model. PLoS One 8:e84281
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

Showing the most recent 10 out of 18 publications