Binding of serum response factor to CArG box sequences is necessary but not sufficient to restrict gene expression to arterial smooth muscle cells.
about
Myocardin is a critical serum response factor cofactor in the transcriptional program regulating smooth muscle cell differentiation.Megakaryoblastic leukemia factor-1 transduces cytoskeletal signals and induces smooth muscle cell differentiation from undifferentiated embryonic stem cellsCardiac hypertrophy and histone deacetylase-dependent transcriptional repression mediated by the atypical homeodomain protein HopHuman SM22 alpha BAC encompasses regulatory sequences for expression in vascular and visceral smooth muscles at fetal and adult stagesUTX, a histone H3-lysine 27 demethylase, acts as a critical switch to activate the cardiac developmental program5' CArG degeneracy in smooth muscle alpha-actin is required for injury-induced gene suppression in vivo.Multiple repressor pathways contribute to phenotypic switching of vascular smooth muscle cells.Prediction of cell type-specific gene modules: identification and initial characterization of a core set of smooth muscle-specific genes.Sm22α transcription occurs at the early onset of the cardiovascular system and the intron 1 is dispensable for its transcription in smooth muscle cells during mouse development.Smad proteins regulate transcriptional induction of the SM22alpha gene by TGF-beta.Increased actin polymerization reduces the inhibition of serum response factor activity by Yin Yang 1.MyoD distal regulatory region contains an SRF binding CArG element required for MyoD expression in skeletal myoblasts and during muscle regeneration.Cell cycle-mediated regulation of smooth muscle alpha-actin gene transcription in fibroblasts and vascular smooth muscle cells involves multiple adenovirus E1A-interacting cofactors.CSRP2, TIMP-1, and SM22alpha promoter fragments direct hepatic stellate cell-specific transgene expression in vitro, but not in vivo.Regulation of SM22 alpha expression by arginine vasopressin and PDGF-BB in vascular smooth muscle cells.Identification of a CArG-independent region of the cysteine-rich protein 2 promoter that directs expression in the developing vasculature.Cis-acting elements, CArG-, E-, CCAAT- and TATA-boxes may be involved in sexually regulated gene transcription in Schistosoma mansoni
P2860
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P2860
Binding of serum response factor to CArG box sequences is necessary but not sufficient to restrict gene expression to arterial smooth muscle cells.
description
2001 nî lūn-bûn
@nan
2001年の論文
@ja
2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
2001年论文
@zh
2001年论文
@zh-cn
name
Binding of serum response fact ...... arterial smooth muscle cells.
@en
type
label
Binding of serum response fact ...... arterial smooth muscle cells.
@en
prefLabel
Binding of serum response fact ...... arterial smooth muscle cells.
@en
P2093
P2860
P356
P1476
Binding of serum response fact ...... o arterial smooth muscle cells
@en
P2093
P2860
P304
16418-16424
P356
10.1074/JBC.M100631200
P407
P577
2001-02-08T00:00:00Z