Triadin deletion induces impaired skeletal muscle function

scientific article published on 19 October 2009

Triadin deletion induces impaired skeletal muscle function is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1074/JBC.M109.022442
P932PMC publication ID2787354
P698PubMed publication ID19843516

P50authorJulie BrocardQ80062105
P2093author name stringIsabelle Marty
David Bendahan
Sarah Oddoux
Jacques Brocard
Benoit Giannesini
Joël Lunardi
Peter Szentesi
Julie Brocard
Julien Fauré
Laszlo Csernoch
Annie Schweitzer
Karine Pernet-Gallay
P2860cites workAbsence of the beta subunit (cchb1) of the skeletal muscle dihydropyridine receptor alters expression of the alpha 1 subunit and eliminates excitation-contraction couplingQ24680364
Modulation of L-type Ca2+ current but not activation of Ca2+ release by the gamma1 subunit of the dihydropyridine receptor of skeletal muscleQ24802046
Complex formation between junctin, triadin, calsequestrin, and the ryanodine receptor. Proteins of the cardiac junctional sarcoplasmic reticulum membraneQ28248323
Enhanced resistance to fatigue and altered calcium handling properties of sarcalumenin knockout miceQ28509838
Cloning and characterization of a new isoform of skeletal muscle triadinQ28575170
Triadin (Trisk 95) overexpression blocks excitation-contraction coupling in rat skeletal myotubesQ28576225
Altered expression of triadin 95 causes parallel changes in localized Ca2+ release events and global Ca2+ signals in skeletal muscle cells in cultureQ28578879
Embryonic lethality and abnormal cardiac myocytes in mice lacking ryanodine receptor type 2.Q28584945
Excitation-contraction uncoupling and muscular degeneration in mice lacking functional skeletal muscle ryanodine-receptor geneQ28587644
Reorganized stores and impaired calcium handling in skeletal muscle of mice lacking calsequestrin-1Q28589478
Caveolin-3 null mice show a loss of caveolae, changes in the microdomain distribution of the dystrophin-glycoprotein complex, and t-tubule abnormalitiesQ28592366
Improved method for accurate and efficient quantification of MRS data with use of prior knowledgeQ32172320
Functional interaction of the cytoplasmic domain of triadin with the skeletal ryanodine receptorQ33859373
Identification of triadin 1 as the predominant triadin isoform expressed in mammalian myocardiumQ33875009
Localization and characterization of the calsequestrin-binding domain of triadin 1. Evidence for a charged beta-strand in mediating the protein-protein interactionQ33896739
The asp-rich region at the carboxyl-terminus of calsequestrin binds to Ca(2+) and interacts with triadinQ33927847
Human skeletal muscle triadin: gene organization and cloning of the major isoform, Trisk 51.Q34186302
Association of triadin with the ryanodine receptor and calsequestrin in the lumen of the sarcoplasmic reticulumQ34308863
Location of ryanodine receptor binding site on skeletal muscle triadinQ34487763
Biochemical evidence for a complex involving dihydropyridine receptor and ryanodine receptor in triad junctions of skeletal muscleQ35103866
Structural analysis of muscle development: transverse tubules, sarcoplasmic reticulum, and the triadQ35491643
Ca(2+) sparks operated by membrane depolarization require isoform 3 ryanodine receptor channels in skeletal muscle.Q35691137
Altered stored calcium release in skeletal myotubes deficient of triadin and junctinQ37060519
Formation of junctions involved in excitation-contraction coupling in skeletal and cardiac muscle.Q37463586
Triadin: what possible function 20 years later?Q37464481
Measurements of ATP binding on the large cytoplasmic loop of the sarcoplasmic reticulum Ca(2+)-ATPase overexpressed in Escherichia coli.Q38309115
Functional coupling between TRPC3 and RyR1 regulates the expressions of key triadic proteinsQ40315222
Metabolic recovery after exercise and the assessment of mitochondrial function in vivo in human skeletal muscle by means of 31P NMR.Q41583686
Localization of the N-terminal and C-terminal ends of triadin with respect to the sarcoplasmic reticulum membrane of rabbit skeletal muscleQ41825445
Triadins are not triad-specific proteins: two new skeletal muscle triadins possibly involved in the architecture of sarcoplasmic reticulumQ41975814
Junctin and calsequestrin overexpression in cardiac muscle: the role of junctin and the synthetic and delivery pathways for the two proteinsQ44524077
Effect of ryanodine receptor mutations on interleukin-6 release and intracellular calcium homeostasis in human myotubes from malignant hyperthermia-susceptible individuals and patients affected by central core diseaseQ45010236
Molecular interaction between ryanodine receptor and glycoprotein triadin involves redox cycling of functionally important hyperreactive sulfhydryls.Q45951705
Localization and partial characterization of the oligomeric disulfide-linked molecular weight 95,000 protein (triadin) which binds the ryanodine and dihydropyridine receptors in skeletal muscle triadic vesiclesQ47427322
Primary structure and topological analysis of a skeletal muscle-specific junctional sarcoplasmic reticulum glycoprotein (triadin)Q48115770
Isolation of a terminal cisterna protein which may link the dihydropyridine receptor to the junctional foot protein in skeletal muscle.Q50877901
In vivo functional analysis of the Hoxa-1 3' retinoic acid response element (3'RARE).Q52197549
Retrograde regulation of store-operated calcium channels by the ryanodine receptor-associated protein triadin 95 in rat skeletal myotubesQ58124984
Molecular interactions of the junctional foot protein and dihydropyridine receptor in skeletal muscle triadsQ68458712
Exploration of delta-subunit interactions in beef heart mitochondrial F1-ATPase by monoclonal antibodiesQ69057196
Specific absence of the alpha 1 subunit of the dihydropyridine receptor in mice with muscular dysgenesisQ69326252
Mechanisms underlying reduced maximum shortening velocity during fatigue of intact, single fibres of mouse muscleQ74645021
Dual regulation of the skeletal muscle ryanodine receptor by triadin and calsequestrinQ77299816
P433issue50
P407language of work or nameEnglishQ1860
P304page(s)34918-34929
P577publication date2009-10-19
P1433published inJournal of Biological ChemistryQ867727
P1476titleTriadin deletion induces impaired skeletal muscle function
P478volume284

Reverse relations

cites work (P2860)
Q35126961A new cytoplasmic interaction between junctin and ryanodine receptor Ca2+ release channels
Q64984483A unique triadin exon deletion causing a null phenotype.
Q24307681Absence of triadin, a protein of the calcium release complex, is responsible for cardiac arrhythmia with sudden death in human
Q28509794Calsequestrin (CASQ1) rescues function and structure of calcium release units in skeletal muscles of CASQ1-null mice
Q104111317Calsequestrin: a well-known but curious protein in skeletal muscle
Q48053644Cannabinoid signalling inhibits sarcoplasmic Ca2+ release and regulates excitation-contraction coupling in mammalian skeletal muscle.
Q34007314Caveolin 3 is associated with the calcium release complex and is modified via in vivo triadin modification
Q51136294Congenital myopathy associated with the triadin knockout syndrome.
Q38970694Core skeletal muscle ryanodine receptor calcium release complex.
Q35063164Cyclization of the intrinsically disordered α1S dihydropyridine receptor II-III loop enhances secondary structure and in vitro function.
Q57181503Deletion of the microtubule-associated protein 6 (MAP6) results in skeletal muscle dysfunction
Q37390949Dietary selenium augments sarcoplasmic calcium release and mechanical performance in mice.
Q42809439Distinct regions of triadin are required for targeting and retention at the junctional domain of the sarcoplasmic reticulum
Q87204696Effects of fluvastatin and coenzyme Q10 on skeletal muscle in normo- and hypercholesterolaemic rats
Q37435413Enhancement of neuromuscular dynamics and strength behavior using extremely low magnitude mechanical signals in mice
Q42046918Excitation-Contraction Coupling Alterations in Myopathies
Q34101915Excitation-contraction coupling and minor triadic proteins in low-frequency fatigue
Q54551370Fluvastatin-induced alterations of skeletal muscle function in hypercholesterolaemic rats.
Q37589625Functional Characterization of a Central Core Disease RyR1 Mutation (p.Y4864H) Associated with Quantitative Defect in RyR1 Protein.
Q90678000Interplay between Triadin and Calsequestrin in the Pathogenesis of CPVT in the Mouse
Q49919753Knockout of human muscle genes revealed by large scale whole-exome studies
Q35193342On the footsteps of Triadin and its role in skeletal muscle
Q37945102Reciprocal dihydropyridine and ryanodine receptor interactions in skeletal muscle activation
Q34642130Reduced gain of excitation-contraction coupling in triadin-null myotubes is mediated by the disruption of FKBP12/RyR1 interaction
Q28078420Review of RyR1 pathway and associated pathomechanisms
Q52639740RyR1 deficiency in congenital myopathies disrupts excitation-contraction coupling.
Q37705608Ryanodine receptor studies using genetically engineered mice
Q35642611The couplonopathies: A comparative approach to a class of diseases of skeletal and cardiac muscle.
Q50587074Three residues in the luminal domain of triadin impact on Trisk 95 activation of skeletal muscle ryanodine receptors.
Q98772000Transcriptome Profiling across Five Tissues of Giant Panda
Q26801317Triadin regulation of the ryanodine receptor complex
Q34329037Triadin/Junctin double null mouse reveals a differential role for Triadin and Junctin in anchoring CASQ to the jSR and regulating Ca(2+) homeostasis
Q97652817Trisk 95 as a novel skin mirror for normal and diabetic systemic glucose level

Search more.