Relatively little is known about how myofibrils are assembled, or how the myofibrils are maintained in the face of repeated muscle activity. This proposal outlines studies of three genes in C. elegans, unc-98, unc-96 and unc-97, which are required for proper myofibril organization. UNC-98 is a novel 310 residue polypeptide consisting of four C2H2 Zn fingers and predicted NLS and NES sequences. By use of UNC-98 antibodies and UNC-98::GFP fusions, UNC-98 resides at M-lines, muscle cell nuclei, and probably at dense bodies (Z line analogs). By 2-hybrid experiments, UNC-98 interacts with UNC-97 (PINCH in mammals), a LIM domain protein required for worm muscle focal adhesion assembly. Like UNC-98, UNC-97::GFP had been shown to localize to muscle dense bodies, M-lines and nuclei. It is hypothesized that UNC-98 and UNC-97 function in muscle focal adhesion homeostasis, in which these proteins when localized to the adhesion sites monitor muscle activity, and travel to the nucleus to affect transcription. Because of their similar mutant phenotypes, genetic interaction, and requirement of unc-96 activity for proper UNC-98 localization, it is hypothesized that UNC-96 and UNC-98 interact or work together. Goals include: (1) study UNC-98 including mapping regions required for nuclear vs. attachment structure localization, to determine whether, UNC-98 moves from myofibrils to the nucleus, to characterize new unc-98 mutant alleles, to characterize several suspected partners and to identify new partners for UNC-98, and to determine whether UNC-98 influences the expression of other genes; (2) to determine the nature of the UNC-96 protein, its intracellular location and molecular partners; and (3) to study UNC-97 including to determine whether UNC-97 moves from myofibrils to nucleus, whether nuclear localization depends on UNC-98, localize UNC-97 with antibodies, seek further evidence for UNC-97's interaction with several known and new proteins, isolate genetic modifiers of unc-97,and to determine whether UNC-97 influences the expression of other genes. ? ?

Agency
National Institute of Health (NIH)
Institute
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Type
Research Project (R01)
Project #
3R01AR052133-01A1S1
Application #
7121021
Study Section
Skeletal Muscle and Exercise Physiology Study Section (SMEP)
Program Officer
Nuckolls, Glen H
Project Start
2005-09-10
Project End
2010-08-31
Budget Start
2005-09-10
Budget End
2006-08-31
Support Year
1
Fiscal Year
2005
Total Cost
$47,048
Indirect Cost
Name
Emory University
Department
Pathology
Type
Schools of Medicine
DUNS #
066469933
City
Atlanta
State
GA
Country
United States
Zip Code
30322
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Warner, Adam; Xiong, Ge; Qadota, Hiroshi et al. (2013) CPNA-1, a copine domain protein, is located at integrin adhesion sites and is required for myofilament stability in Caenorhabditis elegans. Mol Biol Cell 24:601-16
Wilson, Kristy J; Qadota, Hiroshi; Benian, Guy M (2012) Immunofluorescent localization of proteins in Caenorhabditis elegans muscle. Methods Mol Biol 798:171-81
Qadota, Hiroshi; Moerman, Donald G; Benian, Guy M (2012) A molecular mechanism for the requirement of PAT-4 (integrin-linked kinase (ILK)) for the localization of UNC-112 (Kindlin) to integrin adhesion sites. J Biol Chem 287:28537-51
Warner, Adam; Qadota, Hiroshi; Benian, Guy M et al. (2011) The Caenorhabditis elegans paxillin orthologue, PXL-1, is required for pharyngeal muscle contraction and for viability. Mol Biol Cell 22:2551-63
Qadota, Hiroshi; Benian, Guy M (2010) Molecular structure of sarcomere-to-membrane attachment at M-Lines in C. elegans muscle. J Biomed Biotechnol 2010:864749
Moulder, Gary L; Cremona, Gina H; Duerr, Janet et al. (2010) ?-actinin is required for the proper assembly of Z-disk/focal-adhesion-like structures and for efficient locomotion in Caenorhabditis elegans. J Mol Biol 403:516-28
Miller, Rachel K; Qadota, Hiroshi; Stark, Thomas J et al. (2009) CSN-5, a component of the COP9 signalosome complex, regulates the levels of UNC-96 and UNC-98, two components of M-lines in Caenorhabditis elegans muscle. Mol Biol Cell 20:3608-16
Miller, Rachel K; Qadota, Hiroshi; Mercer, Kristina B et al. (2008) UNC-98 and UNC-96 interact with paramyosin to promote its incorporation into thick filaments of Caenorhabditis elegans. Mol Biol Cell 19:1529-39
Stevenson, Tesheka O; Mercer, Kristina B; Cox, Elisabeth A et al. (2007) unc-94 encodes a tropomodulin in Caenorhabditis elegans. J Mol Biol 374:936-50

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