Defective sarcomere assembly in smyd1a and smyd1b zebrafish mutants

scientific article published on 28 February 2019

Defective sarcomere assembly in smyd1a and smyd1b zebrafish mutants is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1096/FJ.201801578R
P932PMC publication ID6463926
P698PubMed publication ID30817176

P2093author name stringFeng He
Zhenjun Tian
Jianshe Zhang
Wuying Chu
Mengxin Cai
Shaojun Du
Lusha Liu
Lichen Han
P2860cites workFunctional analysis of slow myosin heavy chain 1 and myomesin-3 in sarcomere organization in zebrafish embryonic slow muscles.Q38578182
Sarcomere Dysfunction in Nemaline MyopathyQ39258305
Genetic compensation induced by deleterious mutations but not gene knockdowns.Q40744194
Myofibrillogenesis in skeletal muscle cells in zebrafishQ42027499
Proteomic analysis of organ-specific post-translational lysine-acetylation and -methylation in mice by use of anti-acetyllysine and -methyllysine mouse monoclonal antibodiesQ42485737
The chromatin-binding protein Smyd1 restricts adult mammalian heart growthQ42784088
Correction: Still Heart Encodes a Structural HMT, SMYD1b, with Chaperone-Like Function during Fast Muscle Sarcomere AssemblyQ43073585
Methylation, a new epigenetic mark for protein stabilityQ43261361
The UCS factor Steif/Unc-45b interacts with the heat shock protein Hsp90a during myofibrillogenesisQ47073713
The myosin co-chaperone UNC-45 is required for skeletal and cardiac muscle function in zebrafishQ47073763
The myosin-interacting protein SMYD1 is essential for sarcomere organizationQ47073895
mRNA processing in mutant zebrafish lines generated by chemical and CRISPR-mediated mutagenesis produces unexpected transcripts that escape nonsense-mediated decayQ47150815
Zebrafish Embryonic Slow Muscle Is a Rapid System for Genetic Analysis of Sarcomere Organization by CRISPR/Cas9, but Not NgAgoQ49642318
Loss of zebrafish Smyd1a interferes with myofibrillar integrity without triggering the misfolded myosin responseQ50055639
Muscle-specific expression of the smyd1 gene is controlled by its 5.3-kb promoter and 5'-flanking sequence in zebrafish embryos.Q50711281
Defective myogenesis in the absence of the muscle-specific lysine methyltransferase SMYD1.Q51598998
siRNA-mediated inhibition of skNAC and Smyd1 expression disrupts myofibril organization: Immunofluorescence and electron microscopy study in C2C12 cells.Q52369214
The sarcomere and sarcomerogenesis.Q52591693
The sequence of the NH2-terminal 204-residue fragment of the heavy chain of rabbit skeletal muscle myosinQ71070903
Histone methyltransferase Smyd1 regulates mitochondrial energetics in the heartQ90646232
Genome-wide survey and developmental expression mapping of zebrafish SET domain-containing genesQ21562301
skNAC, a Smyd1-interacting transcription factor, is involved in cardiac development and skeletal muscle growth and regenerationQ24306754
SMYD1, the myogenic activator, is a direct target of serum response factor and myogeninQ24318909
Efficient genome editing in zebrafish using a CRISPR-Cas systemQ24610828
SMYD proteins: key regulators in skeletal and cardiac muscle development and functionQ26865167
m-Bop, a repressor protein essential for cardiogenesis, interacts with skNAC, a heart- and muscle-specific transcription factorQ28217589
Targeting the sarcomere to correct muscle functionQ28260629
How to build a myofibrilQ28296222
BOP, a regulator of right ventricular heart development, is a direct transcriptional target of MEF2C in the developing heartQ28505957
Bop encodes a muscle-restricted protein containing MYND and SET domains and is essential for cardiac differentiation and morphogenesisQ28587459
The ATPase-dependent chaperoning activity of Hsp90a regulates thick filament formation and integration during skeletal muscle myofibrillogenesisQ28754755
High-resolution in situ hybridization to whole-mount zebrafish embryosQ29617529
Heat-shock protein 90alpha1 is required for organized myofibril assembly in skeletal muscles of zebrafish embryos.Q30481082
Knockdown and overexpression of Unc-45b result in defective myofibril organization in skeletal muscles of zebrafish embryos.Q33694916
Frameshift indels introduced by genome editing can lead to in-frame exon skipping.Q33751947
SmyD1, a histone methyltransferase, is required for myofibril organization and muscle contraction in zebrafish embryos.Q34928212
Reverse genetic screening reveals poor correlation between morpholino-induced and mutant phenotypes in zebrafish.Q35806361
In vivo protein trapping produces a functional expression codex of the vertebrate proteomeQ35835730
SMYD1 and G6PD modulation are critical events for miR-206-mediated differentiation of rhabdomyosarcomaQ36186504
Mouse myofibers lacking the SMYD1 methyltransferase are susceptible to atrophy, internalization of nuclei and myofibrillar disarrayQ36802641
Efficient multiplex biallelic zebrafish genome editing using a CRISPR nuclease systemQ37117695
Smyd1b is required for skeletal and cardiac muscle function in zebrafishQ37306191
Expression and functional characterization of Smyd1a in myofibril organization of skeletal musclesQ37510551
Lysine methylation of nonhistone proteins is a way to regulate their stability and function.Q37772914
Lysine methylation: beyond histonesQ37970950
skNAC and Smyd1 in transcriptional controlQ38297716
P433issue5
P304page(s)6209-6225
P577publication date2019-02-28
P1433published inFASEB JournalQ520194
P1476titleDefective sarcomere assembly in smyd1a and smyd1b zebrafish mutants
P478volume33

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cites work (P2860)
Q90412003Modeling Neuronal Diseases in Zebrafish in the Era of CRISPR
Q99399885Under construction: The dynamic assembly, maintenance, and degradation of the cardiac sarcomere
Q91986334Zebrafish models of sarcopenia

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