Click here to close
Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly.
We suggest using a current version of Chrome,
FireFox, or Safari.
Caenorhabditis elegans UNC-96 is a new component of M-lines that interacts with UNC-98 and paramyosin and is required in adult muscle for assembly and/or maintenance of thick filaments.
???displayArticle.abstract???
To gain further insight into the molecular architecture, assembly, and maintenance of the sarcomere, we have carried out a molecular analysis of the UNC-96 protein in the muscle of Caenorhabditis elegans. By polarized light microscopy of body wall muscle, unc-96 mutants display reduced myofibrillar organization and characteristic birefringent "needles." By immunofluorescent staining of known myofibril components, unc-96 mutants show major defects in the organization of M-lines and in the localization of a major thick filament component, paramyosin. In unc-96 mutants, the birefringent needles, which contain both UNC-98 and paramyosin, can be suppressed by starvation or by exposure to reduced temperature. UNC-96 is a novel approximately 47-kDa polypeptide that has no recognizable domains. Antibodies generated to UNC-96 localize the protein to the M-line, a region of the sarcomere in which thick filaments are cross-linked. By genetic and biochemical criteria, UNC-96 interacts with UNC-98, a previously described component of M-lines, and paramyosin. Additionally, UNC-96 copurifies with native thick filaments. A model is presented in which UNC-96 is required in adult muscle to promote thick filament assembly and/or maintenance.
Barral,
Unc-45 mutations in Caenorhabditis elegans implicate a CRO1/She4p-like domain in myosin assembly.
1998, Pubmed
Barral,
Unc-45 mutations in Caenorhabditis elegans implicate a CRO1/She4p-like domain in myosin assembly.
1998,
Pubmed Barral,
Role of the myosin assembly protein UNC-45 as a molecular chaperone for myosin.
2002,
Pubmed Barstead,
Vinculin is essential for muscle function in the nematode.
1991,
Pubmed Benian,
Sequence of an unusually large protein implicated in regulation of myosin activity in C. elegans.
1989,
Pubmed Benian,
Additional sequence complexity in the muscle gene, unc-22, and its encoded protein, twitchin, of Caenorhabditis elegans.
1993,
Pubmed Benian,
The Caenorhabditis elegans gene unc-89, required fpr muscle M-line assembly, encodes a giant modular protein composed of Ig and signal transduction domains.
1996,
Pubmed Bodine,
Identification of ubiquitin ligases required for skeletal muscle atrophy.
2001,
Pubmed Broday,
The LIM domain protein UNC-95 is required for the assembly of muscle attachment structures and is regulated by the RING finger protein RNF-5 in C. elegans.
2004,
Pubmed Centner,
Identification of muscle specific ring finger proteins as potential regulators of the titin kinase domain.
2001,
Pubmed Deitiker,
Thick filament substructures in Caenorhabditis elegans: evidence for two populations of paramyosin.
1993,
Pubmed Didier,
RNF5, a RING finger protein that regulates cell motility by targeting paxillin ubiquitination and altered localization.
2003,
Pubmed Epstein,
Myosin and paramyosin of Caenorhabditis elegans embryos assemble into nascent structures distinct from thick filaments and multi-filament assemblages.
1993,
Pubmed Epstein,
Myosin and paramyosin are organized about a newly identified core structure.
1985,
Pubmed Epstein,
Purified thick filaments from the nematode Caenorhabditis elegans: evidence for multiple proteins associated with core structures.
1988,
Pubmed Epstein,
A mutant affecting the heavy chain of myosin in Caenorhabditis elegans.
1974,
Pubmed Epstein,
Preliminary three-dimensional model for nematode thick filament core.
1995,
Pubmed Ferrara,
Titin/connectin-related proteins in C. elegans: a review and new findings.
2005,
Pubmed Flaherty,
Titins in C.elegans with unusual features: coiled-coil domains, novel regulation of kinase activity and two new possible elastic regions.
2002,
Pubmed Francis,
Muscle organization in Caenorhabditis elegans: localization of proteins implicated in thin filament attachment and I-band organization.
1985,
Pubmed Gengyo-Ando,
Single charge change on the helical surface of the paramyosin rod dramatically disrupts thick filament assembly in Caenorhabditis elegans.
1991,
Pubmed Gettner,
Characterization of beta pat-3 heterodimers, a family of essential integrin receptors in C. elegans.
1995,
Pubmed Gotthardt,
Conditional expression of mutant M-line titins results in cardiomyopathy with altered sarcomere structure.
2003,
Pubmed Gräter,
Mechanically induced titin kinase activation studied by force-probe molecular dynamics simulations.
2005,
Pubmed Gregorio,
To the heart of myofibril assembly.
2000,
Pubmed Hannak,
The kinetically dominant assembly pathway for centrosomal asters in Caenorhabditis elegans is gamma-tubulin dependent.
2002,
Pubmed Hill,
dpy-18 encodes an alpha-subunit of prolyl-4-hydroxylase in caenorhabditis elegans.
2000,
Pubmed Hobert,
A conserved LIM protein that affects muscular adherens junction integrity and mechanosensory function in Caenorhabditis elegans.
1999,
Pubmed Hoppe,
Regulation of the myosin-directed chaperone UNC-45 by a novel E3/E4-multiubiquitylation complex in C. elegans.
2004,
Pubmed Hresko,
Assembly of body wall muscle and muscle cell attachment structures in Caenorhabditis elegans.
1994,
Pubmed Ito,
Transformation of intact yeast cells treated with alkali cations.
1983,
Pubmed James,
Genomic libraries and a host strain designed for highly efficient two-hybrid selection in yeast.
1996,
Pubmed Kagawa,
Paramyosin gene (unc-15) of Caenorhabditis elegans. Molecular cloning, nucleotide sequence and models for thick filament structure.
1989,
Pubmed Kamath,
Genome-wide RNAi screening in Caenorhabditis elegans.
2003,
Pubmed Knappeis,
The ultrastructure of the M line in skeletal muscle.
1968,
Pubmed Lange,
The kinase domain of titin controls muscle gene expression and protein turnover.
2005,
Pubmed Lin,
C. elegans PAT-6/actopaxin plays a critical role in the assembly of integrin adhesion complexes in vivo.
2003,
Pubmed Liu,
Differential assembly of alpha- and gamma-filagenins into thick filaments in Caenorhabditis elegans.
2000,
Pubmed Luther,
Three-dimensional structure of the vertebrate muscle M-region.
1978,
Pubmed Mackinnon,
C. elegans PAT-4/ILK functions as an adaptor protein within integrin adhesion complexes.
2002,
Pubmed Maruyama,
Myosin heavy chain gene amplification as a suppressor mutation in Caenorhabditis elegans.
1989,
Pubmed Mercer,
Caenorhabditis elegans UNC-98, a C2H2 Zn finger protein, is a novel partner of UNC-97/PINCH in muscle adhesion complexes.
2003,
Pubmed
,
Xenbase Miller,
Immunological identification of the genes encoding the four myosin heavy chain isoforms of Caenorhabditis elegans.
1986,
Pubmed Miller,
Differential localization of two myosins within nematode thick filaments.
1983,
Pubmed Minamide,
A filter paper dye-binding assay for quantitative determination of protein without interference from reducing agents or detergents.
1990,
Pubmed Mitch,
Mechanisms of muscle wasting. The role of the ubiquitin-proteasome pathway.
1996,
Pubmed Moerman,
Identification and intracellular localization of the unc-22 gene product of Caenorhabditis elegans.
1988,
Pubmed Moerman,
Sarcomere assembly in C. elegans muscle.
2006,
Pubmed Moulder,
Talin requires beta-integrin, but not vinculin, for its assembly into focal adhesion-like structures in the nematode Caenorhabditis elegans.
1996,
Pubmed Müller,
STEM Analysis of Caenorhabditis elegans muscle thick filaments: evidence for microdifferentiated substructures.
2001,
Pubmed Nonet,
Synaptic function is impaired but not eliminated in C. elegans mutants lacking synaptotagmin.
1993,
Pubmed Ono,
The Caenorhabditis elegans unc-78 gene encodes a homologue of actin-interacting protein 1 required for organized assembly of muscle actin filaments.
2001,
Pubmed Riddle,
Indirect suppression in Caenorhabditis elegans.
1978,
Pubmed Riddle,
Muscle: Structure, Function, and Development
1997,
Pubmed Rogalski,
Products of the unc-52 gene in Caenorhabditis elegans are homologous to the core protein of the mammalian basement membrane heparan sulfate proteoglycan.
1993,
Pubmed Rogalski,
The UNC-112 gene in Caenorhabditis elegans encodes a novel component of cell-matrix adhesion structures required for integrin localization in the muscle cell membrane.
2000,
Pubmed Schachat,
Myosins exist as homodimers of heavy chains: demonstration with specific antibody purified by nematode mutant myosin affinity chromatography.
1978,
Pubmed Simmer,
Loss of the putative RNA-directed RNA polymerase RRF-3 makes C. elegans hypersensitive to RNAi.
2002,
Pubmed Small,
Three new isoforms of Caenorhabditis elegans UNC-89 containing MLCK-like protein kinase domains.
2004,
Pubmed Soto,
The GEX-2 and GEX-3 proteins are required for tissue morphogenesis and cell migrations in C. elegans.
2002,
Pubmed Tsuboi,
Isolation of the interacting molecules with GEX-3 by a novel functional screening.
2002,
Pubmed Waterston,
The minor myosin heavy chain, mhcA, of Caenorhabditis elegans is necessary for the initiation of thick filament assembly.
1989,
Pubmed Waterston,
Mutants with altered muscle structure of Caenorhabditis elegans.
1980,
Pubmed Waterston,
Mutants affecting paramyosin in Caenorhabditis elegans.
1977,
Pubmed Waterston,
Paramyosin of Caenorhabditis elegans.
1974,
Pubmed Weiner,
Spatial control of actin polymerization during neutrophil chemotaxis.
1999,
Pubmed Williams,
Genes critical for muscle development and function in Caenorhabditis elegans identified through lethal mutations.
1994,
Pubmed Zengel,
Identification of genetic elements associated with muscle structure in the nematode Caenorhabditis elegans.
1980,
Pubmed