Cargando…

CPNA-1, a copine domain protein, is located at integrin adhesion sites and is required for myofilament stability in Caenorhabditis elegans

We identify cpna-1 (F31D5.3) as a novel essential muscle gene in the nematode Caenorhabditis elegans. Antibodies specific to copine domain protein atypical-1 (CPNA-1), as well as a yellow fluorescent protein translational fusion, are localized to integrin attachment sites (M-lines and dense bodies)...

Descripción completa

Detalles Bibliográficos
Autores principales:	Warner, Adam, Xiong, Ge, Qadota, Hiroshi, Rogalski, Teresa, Vogl, A. Wayne, Moerman, Donald G., Benian, Guy M.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	The American Society for Cell Biology 2013
Materias:	Articles
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3583664/ https://www.ncbi.nlm.nih.gov/pubmed/23283987 http://dx.doi.org/10.1091/mbc.E12-06-0478

Ejemplares similares

The Caenorhabditis elegans paxillin orthologue, PXL-1, is required for pharyngeal muscle contraction and for viability
por: Warner, Adam, et al.
Publicado: (2011)

Caenorhabditis elegans SORB-1 localizes to integrin adhesion sites and is required for organization of sarcomeres and mitochondria in myocytes
por: Loveless, Timothy, et al.
Publicado: (2017)

An Integrated Strategy to Study Muscle Development and Myofilament Structure in Caenorhabditis elegans
por: Meissner, Barbara, et al.
Publicado: (2009)

UNC-98 links an integrin-associated complex to thick filaments in Caenorhabditis elegans muscle
por: Miller, Rachel K., et al.
Publicado: (2006)

Twitchin kinase interacts with MAPKAP kinase 2 in Caenorhabditis elegans striated muscle
por: Matsunaga, Yohei, et al.
Publicado: (2015)

The UNC-112 Gene in Caenorhabditis elegansEncodes a Novel Component of Cell–Matrix Adhesion Structures Required for Integrin Localization in the Muscle Cell Membrane
por: Rogalski, Teresa M., et al.
Publicado: (2000)

Molecular Structure of Sarcomere-to-Membrane Attachment at M-Lines in C. elegans Muscle
por: Qadota, Hiroshi, et al.
Publicado: (2010)

UNC-89 (obscurin) binds to MEL-26, a BTB-domain protein, and affects the function of MEI-1 (katanin) in striated muscle of Caenorhabditis elegans
por: Wilson, Kristy J., et al.
Publicado: (2012)

ZYX-1, the unique zyxin protein of Caenorhabditis elegans, is involved in dystrophin-dependent muscle degeneration
por: Lecroisey, Claire, et al.
Publicado: (2013)

Determining the Sub-Cellular Localization of Proteins within Caenorhabditis elegans Body Wall Muscle
por: Meissner, Barbara, et al.
Publicado: (2011)

Protein phosphatase 2A is crucial for sarcomere organization in Caenorhabditis elegans striated muscle
por: Qadota, Hiroshi, et al.
Publicado: (2018)

FARL-11 (STRIP1/2) is required for sarcomere and sarcoplasmic reticulum organization in C. elegans
por: Martin, Sterling C. T., et al.
Publicado: (2023)

Phosphatidylserine exposure promotes increased adhesion in Dictyostelium Copine A mutants
por: Ide, Amber D., et al.
Publicado: (2021)

The SH3 domain of UNC-89 (obscurin) interacts with paramyosin, a coiled-coil protein, in Caenorhabditis elegans muscle
por: Qadota, Hiroshi, et al.
Publicado: (2016)

An approach for exploring interaction between two proteins in vivo
por: Qadota, Hiroshi, et al.
Publicado: (2014)

Big Data in Caenorhabditis elegans: quo vadis?
por: Hutter, Harald, et al.
Publicado: (2015)

Copine A Interacts with Actin Filaments and Plays a Role in Chemotaxis and Adhesion
por: Buccilli, Matthew J., et al.
Publicado: (2019)

Conformational changes in twitchin kinase in vivo revealed by FRET imaging of freely moving C. elegans
por: Porto, Daniel, et al.
Publicado: (2021)

UNC-60B, an ADF/Cofilin Family Protein, Is Required for Proper Assembly of Actin into Myofibrils in Caenorhabditis elegans Body Wall Muscle
por: Ono, Shoichiro, et al.
Publicado: (1999)

Muscle contraction phenotypic analysis enabled by optogenetics reveals functional relationships of sarcomere components in Caenorhabditis elegans
por: Hwang, Hyundoo, et al.
Publicado: (2016)

Missense mutation of a conserved residue in UNC-112 (kindlin) eliminates binding to PAT-4 (ILK)
por: Qadota, Hiroshi, et al.
Publicado: (2021)

Investigating the correlation of muscle function tests and sarcomere organization in C. elegans
por: Lesanpezeshki, Leila, et al.
Publicado: (2021)

Large Isoforms of UNC-89 (Obscurin) Are Required for Muscle Cell Architecture and Optimal Calcium Release in Caenorhabditis elegans
por: Spooner, Patrick M., et al.
Publicado: (2012)

Overexpression of Copines‐1 is associated with clinicopathological parameters and poor outcome in gastric cancer
por: Yang, Jun, et al.
Publicado: (2022)

α spectrin is essential for morphogenesis and body wall muscle formation in Caenorhabditis elegans
por: Norman, Kenneth R., et al.
Publicado: (2002)

Genetic analysis of the interaction between the N- and C-terminal halves of UNC-112 (kindlin)
por: Qadota, Hiroshi, et al.
Publicado: (2020)

Copy number variation in the genomes of twelve natural isolates of Caenorhabditis elegans
por: Maydan, Jason S, et al.
Publicado: (2010)

Calpains Mediate Integrin Attachment Complex Maintenance of Adult Muscle in Caenorhabditis elegans
por: Etheridge, Timothy, et al.
Publicado: (2012)

Modeling neurodegeneration in Caenorhabditis elegans
por: Caldwell, Kim A., et al.
Publicado: (2020)

The Myofilament Lattice: Studies on Isolated Fibers : III. The effect of myofilament spacing upon tension
por: April, Ernest W., et al.
Publicado: (1973)

The Myosin Chaperone UNC-45 Is Organized in Tandem Modules to Support Myofilament Formation in C. elegans
por: Gazda, Linn, et al.
Publicado: (2013)

Copine A regulates the size and exocytosis of contractile vacuoles and postlysosomes in Dictyostelium
por: Wight, Elise M., et al.
Publicado: (2020)

The C. elegans UNC-23 protein, a member of the BCL-2-associated athanogene (BAG) family of chaperone regulators, interacts with HSP-1 to regulate cell attachment and maintain hypodermal integrity
por: Rahmani, Poupak, et al.
Publicado: (2015)

Caenorhabditis Elegans
Publicado: (2000)

Mutation location of HCM-causing troponin T mutations defines the degree of myofilament dysfunction in human cardiomyocytes
por: Schuldt, Maike, et al.
Publicado: (2021)

Upregulation of Copine1 in trabecular meshwork cells of POAG patients: a membrane proteomics approach
por: Zhang, Yuehong, et al.
Publicado: (2008)

Transcriptome analysis for Caenorhabditis elegans based on novel expressed sequence tags
por: Shin, Heesun, et al.
Publicado: (2008)

A quantitative medium-throughput assay to measure Caenorhabditis elegans development and reproduction
por: Wittkowski, Paul, et al.
Publicado: (2020)

The calcium sensor Copine-6 regulates spine structural plasticity and learning and memory
por: Reinhard, Judith R., et al.
Publicado: (2016)

Molecular studies into cell biological role of Copine-4 in Retinal Ganglion Cells
por: Goel, Manvi, et al.
Publicado: (2021)

Cannot write session to /tmp/vufind_sessions/sess_3g7sa1uvfhukm0l3aj38fogfg5