Depletion of zebrafish Tcap leads to muscular dystrophy via disrupting sarcomere-membrane interaction, not sarcomere assembly

scientific article

Depletion of zebrafish Tcap leads to muscular dystrophy via disrupting sarcomere-membrane interaction, not sarcomere assembly is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1093/HMG/DDP362
P932PMC publication ID2758143
P698PubMed publication ID19679566
P5875ResearchGate publication ID26740867

P50authorJingchun YangQ40070445
P2093author name stringXiaolei Xu
Ruilin Zhang
Jin Zhu
P2860cites workStructural basis for activation of the titin kinase domain during myofibrillogenesisQ22004264
Specific interaction of the potassium channel β-subunit minK with the sarcomeric protein T-cap suggests a T-tubule-myofibril linking systemQ24291879
Telethonin and Other New Proteins of the Z‐Disc of Skeletal MuscleQ24291885
Calsarcin-3, a novel skeletal muscle-specific member of the calsarcin family, interacts with multiple Z-disc proteinsQ24292289
Interaction of BMP10 with Tcap may modulate the course of hypertensive cardiac hypertrophyQ24296709
The cardiac mechanical stretch sensor machinery involves a Z disc complex that is defective in a subset of human dilated cardiomyopathyQ24337914
Amphiphysin is necessary for organization of the excitation-contraction coupling machinery of muscles, but not for synaptic vesicle endocytosis in DrosophilaQ24600060
The zebrafish candyfloss mutant implicates extracellular matrix adhesion failure in laminin alpha2-deficient congenital muscular dystrophyQ24681141
Zebrafish as a model for caveolin-associated muscle disease; caveolin-3 is required for myofibril organization and muscle cell patterning.Q47074190
Conditional expression of mutant M-line titins results in cardiomyopathy with altered sarcomere structureQ47614862
High-frequency generation of transgenic zebrafish which reliably express GFP in whole muscles or the whole body by using promoters of zebrafish origin.Q52191295
The Ankrd2 Protein, a Link Between the Sarcomere and the Nucleus in Skeletal MuscleQ55868727
Limb–girdle muscular dystrophiesQ57390105
Deficiency of a glycoprotein component of the dystrophin complex in dystrophic muscleQ59089242
The molecular basis of muscular dystrophy in the mdx mouse: a point mutationQ69514522
Loss of myotubularin function results in T-tubule disorganization in zebrafish and human myotubular myopathyQ27313067
The complete sequence of dystrophin predicts a rod-shaped cytoskeletal proteinQ28118471
Telethonin, a novel sarcomeric protein of heart and skeletal muscleQ28118954
The novel sarcomeric protein telethonin exhibits developmental and functional regulationQ28141908
Limb-girdle muscular dystrophy type 2G is caused by mutations in the gene encoding the sarcomeric protein telethoninQ28143777
Dysferlin Interacts with Annexins A1 and A2 and Mediates Sarcolemmal Wound-healingQ28204713
Early and selective disappearance of telethonin protein from the sarcomere in neurogenic atrophyQ28213994
Titin-cap associates with, and regulates secretion of, MyostatinQ28220596
The Ankrd2 protein, a link between the sarcomere and the nucleus in skeletal muscleQ28261059
Two immunoglobulin‐like domains of the Z‐disc portion of titin interact in a conformation‐dependent way with telethoninQ28275024
Protein kinase D is a novel mediator of cardiac troponin I phosphorylation and regulates myofilament functionQ28290449
Palindromic assembly of the giant muscle protein titin in the sarcomeric Z-diskQ28291323
Caveolin-3 null mice show a loss of caveolae, changes in the microdomain distribution of the dystrophin-glycoprotein complex, and t-tubule abnormalitiesQ28592366
Effective targeted gene 'knockdown' in zebrafishQ29547445
The sarcomeric Z-disc: a nodal point in signalling and diseaseQ34485166
Wnt3a regulates the development of cardiac neural crest cells by modulating expression of cysteine-rich intestinal protein 2 in rhombomere 6.Q34753546
Zebrafish integrin-linked kinase is required in skeletal muscles for strengthening the integrin-ECM adhesion complexQ34774115
Muscular dystrophies: genes to pathogenesisQ35145855
The zebrafish as a model for muscular dystrophy and congenital myopathyQ35540869
Cardiac mechanotransduction and implications for heart diseaseQ35556827
At the crossroads of myocardial signaling: the role of Z-discs in intracellular signaling and cardiac function.Q35672020
Dystrophin protects the sarcolemma from stresses developed during muscle contractionQ36259954
Modeling human muscle disease in zebrafishQ36578338
Molecular mechanisms of muscular dystrophies: old and new playersQ36593241
Signaling mechanisms involved in disuse muscle atrophyQ36766059
Transcription-terminating mutation in telethonin causing autosomal recessive muscular dystrophy type 2G in a European patientQ36992611
Amphiphysin 2 (Bin1) and T-tubule biogenesis in muscleQ40710117
Dynamics of Z-band based proteins in developing skeletal muscle cellsQ41437699
The expanding phenotype of POMT1 mutations: from Walker-Warburg syndrome to congenital muscular dystrophy, microcephaly, and mental retardation.Q41919724
Transient and transgenic analysis of the zebrafish ventricular myosin heavy chain (vmhc) promoter: an inhibitory mechanism of ventricle-specific gene expressionQ41974233
Electron microscopic examination of basal lamina in Fukuyama congenital muscular dystrophyQ42439618
Depletion of zebrafish titin reduces cardiac contractility by disrupting the assembly of Z-discs and A-bandsQ42575972
Integrin-linked kinase, a novel component of the cardiac mechanical stretch sensor, controls contractility in the zebrafish heartQ42850406
A GFP-based genetic screen reveals mutations that disrupt the architecture of the zebrafish retinotectal projectionQ46522442
Dystrophin is required for the formation of stable muscle attachments in the zebrafish embryoQ47073103
Obscurin is required for the lateral alignment of striated myofibrils in zebrafish.Q47073208
P433issue21
P921main subjectDanio rerioQ169444
muscular dystrophyQ1137767
Titin-cap (telethonin)Q29821770
P304page(s)4130-4140
P577publication date2009-08-12
P1433published inHuman Molecular GeneticsQ2720965
P1476titleDepletion of zebrafish Tcap leads to muscular dystrophy via disrupting sarcomere-membrane interaction, not sarcomere assembly
P478volume18

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cites work (P2860)
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Q36252345α‐Actinin2 is required for the lateral alignment ofZdiscs and ventricular chamber enlargement during zebrafish cardiogenesis

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