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Mrf4 (myf6) is dynamically expressed in differentiated zebrafish skeletal muscle
mrf4 but not myog (Montrer MYOG Kits ELISA) can fully rescue myogenesis in the myod (Montrer MYOD1 Kits ELISA)/myf5 (Montrer MYF5 Kits ELISA) double morphant via a selective and robust activation of myod (Montrer MYOD1 Kits ELISA). Rescue does not happen spontaneously, because the gene is expressed only at the onset of muscle differentiation
findings identified miR (Montrer MLXIP Kits ELISA)-374b directly targets Myf6 and negatively regulates myogenesis
Mrf4 has a role in priming embryonic founder cells to become adult muscle stem cells
Intrinsic muscle factor MRF4 plays an important role in maintenance of neuromuscular junctions.
Data demonstrated that Myf6 is Tceal7 (Montrer TCEAL7 Kits ELISA) upstream transactivators using transcriptional assays.
MRF4 targets the proximal region of M-cadherin promoter and bind the E4-box.
Hox (Montrer MSH2 Kits ELISA) genes produce global patterns in the axial skeleton; Myf5 (Montrer MYF5 Kits ELISA) and Myf6 have roles in rib formation
Mrf4 expression precedes or is contemporaneous with that of Myf5 (Montrer MYF5 Kits ELISA), suggesting that this transcription factor plays a hitherto unsuspected role in myogenesis
an enhancer element directs MRF4 gene expression primarily in fast muscle fibers
elements within a 7.5-kb promoter fragment of the MRF4 gene are sufficient to drive the embryonic wave of expression very similar to the endogenous gene in somites of mouse embryos
skeletal muscle is present in the new Myf5 (Montrer MYF5 Kits ELISA):Myod (Montrer MYOD1 Kits ELISA) double-null mice only when Mrf4 expression is not compromised
A conserved myf6 promoter drives transgenic expression in Xenopus embryonic somites and adult muscle.
XMRF4 protein does not require innervation during muscle regeneration
XMRF4 protein accumulated in somite nuclei slightly after XMRF4 transcripts
The myogenic basic helix-loop-helix family of transcription factors, MyoD (Montrer MYOD1 Kits ELISA), Myf5 (Montrer MYF5 Kits ELISA), myogenin (Montrer MYOG Kits ELISA), and MRF4, can each activate the muscle differentiation program.
Myogenin (Montrer MYOG Kits ELISA) and myogenic differentiation factor D (MyoD (Montrer MYOD1 Kits ELISA)) mRNAs increased (P < 0.05) in young and old, whereas myogenic factor (Montrer MYOG Kits ELISA) (myf)-5 (Montrer MYF5 Kits ELISA) mRNA increased in young only (P < 0.05). Myf-6 protein increased (P < 0.05) in both young and old.
Pietrain pigs exhibited significant higher expression of MYF6 and hypermethylated E2F1 (Montrer E2F1 Kits ELISA) binding element within MYF6 5'-regulatory region as compared with Duroc pigs.
The expression level of Myf6 gene does not indicate significant differences between muscles, ages and breeds.
The porcine MYF6 gene was amplified and sequenced and compared with MYF6 gene sequences of other species. The amino acid sequence was deduced and an interspecies homology analysis was performed.
Associations between the genotype at the MYF6 locus and carcass quality traits appeared to be breed-dependent.
MRF4 and H-FABP (Montrer FABP3 Kits ELISA) genes are associated with growth traits in Qinchuan cattle and related hybrids [MRF4]
The protein encoded by this gene is a probable basic helix-loop-helix (bHLH) DNA binding protein involved in muscle differentiation. The encoded protein likely acts as a heterodimer with another bHLH protein. Defects in this gene are a cause of autosomal dominant centronuclear myopathy (ADCNM).
myogenic factor 6
, myogenic factor 6 (herculin)
, muscle-specific regulatory factor 4
, Myogenic factor 6 (herculin)
, myogenic factor 6 b
, class C basic helix-loop-helix protein 4
, myogenic factor 6, transcription activator
, myogenic factor 6 a
, skeletal muscle-specific DNA-binding protein