This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. Primary support for the subproject and the subproject's principal investigator may have been provided by other sources, including other NIH sources. The Total Cost listed for the subproject likely represents the estimated amount of Center infrastructure utilized by the subproject, not direct funding provided by the NCRR grant to the subproject or subproject staff. Determining the molecular mechanisms involved in the differentiation of post mitotic cells such as striated muscle cells, will be crucial for understanding and controlling the way in which tissue regeneration occurs and extremely valuable for the use of stem cell therapies. Master regulators likely play a key role in assuring normal development of tissue-specific structures and function, some of which must link differentiation signaling to pathways which regulate both apoptosis and cell cycle withdrawal. Though the mechanisms which regulate these complex signaling networks are by and large not understood, posttranslational modification of proteins by phosphorylation, acetylation and ubiquitylation, as well as alternative splicing of mRNA transcripts are essential for generating the precise spacio-temporal patterns of protein activation which are required. Ufd2a is critical to cell division and may also participate in apoptosis signaling. In addition, while undifferentiated myoblasts express exclusively a shorter, ubiquitous form of Ufd2a, fully differentiated cardiac and skeletal muscle cells express a larger, alternatively spliced isoform. Ufd2a appears to be critical to normal development of the heart as Ufd2a -/- mice die in utero with multiple heart defects. The goal of this proposal is to define the spacio-temporal regulation of Ufd2a by alternative splicing, and to determine the functional significance of these tissue-specific isoforms in the process of development and differentiation. These studies may provide insights into how non-dividing cells may employ critical cell cycle effectors for novel functions during their differentiation and lead to a better understanding of the mechanisms of cardiac and skeletal muscle development.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Exploratory Grants (P20)
Project #
5P20RR016457-11
Application #
8360077
Study Section
Special Emphasis Panel (ZRR1-RI-4 (01))
Project Start
2011-05-01
Project End
2012-04-30
Budget Start
2011-05-01
Budget End
2012-04-30
Support Year
11
Fiscal Year
2011
Total Cost
$77,034
Indirect Cost
Name
University of Rhode Island
Department
Pharmacology
Type
Schools of Pharmacy
DUNS #
144017188
City
Kingston
State
RI
Country
United States
Zip Code
02881
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