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Selenoprotein W is conserved in human, rhesus monkey, sheep, rat, and mouse.
SelW may have a regulatory function in redox cell signaling by interacting with 14-3-3 protein (显示 YWHAE 抗体).
Suppression of EGFR (显示 EGFR 抗体) ubiquitination by SEPW1 may be related to the putative increase in cancer risk associated with high selenium intakes.
In response to selenium compounds, SepW1 synthesis increased at the protein and the mRNA levels.
SEPW1 silencing increases MKK4 (显示 MAP2K4 抗体), which activates p38gamma (显示 MAPK12 抗体), p38delta, and JNK2 (显示 MAPK9 抗体) to phosphorylate p53 (显示 TP53 抗体) on Ser (显示 SIGLEC1 抗体)-33 and cause a transient G(1) arrest.
p53 (显示 TP53 抗体) was increased in SEPW1 silenced cells and was inversely correlated with SEPW1 mRNA in cell lines with altered SEPW1 expression.
The present work shows that SEPW1 facilitates the G1 to S-phase transition by down-regulating expression of the cyclin-dependent kinase (显示 CDK1 抗体) inhibitor p21 (显示 CDKN1A 抗体)
The gene lacks canonical TATA and CAAT boxes, but has numerous Sp1 (显示 PSG1 抗体) consensus binding sites upstream of multiple transcription start sites. SEPW1 is expressed in all of the 22 tissues assayed, and shows highest expression in skeletal muscle and heart.
SelW expression in the colon is highly sensitive to Se-depletion
SeW is the novel molecular target of MeHg in human neuronal cells and down-regulation of this selenoenzyme by MeHg is dependent not on generation of ROS (显示 ROS1 抗体) but on depletion of GSH.
SEPW1 mRNA levels were maximal during G1-phase, dropped after the G1/S transition and increased again after G2/M-phase.
SelW enhances myoblast differentiation by inhibiting TAZ (显示 TAZ 抗体) binding to 14-3-3 (显示 YWHAQ 抗体).
SelW gene was activated by the binding of MyoD (显示 MYOD1 抗体) to a specific E-box during early skeletal muscle differentiation.
The main function of SelW in muscle cells is not in the antioxidative system.
Data show that the loss of SelT (显示 SELT 抗体) elevates expression of another selenoprotein, selenoprotein W, suggesting that SepW1 may functionally compensate for SelT (显示 SELT 抗体).
Selenoprotein W is involved in muscle growth and differentiation by protecting the developing myoblasts from oxidative stress
increased in mouse brains of postnatal day 8 and 20 relative to embryonic day 15; siRNA-transfected neurons are more sensitive to the oxidative stress-induced (显示 SQSTM1 抗体) apoptosis
This gene encodes a selenoprotein, which contains a selenocysteine (Sec) residue at its active site. The selenocysteine is encoded by the UGA codon that normally signals translation termination. The 3' UTR of selenoprotein genes have a common stem-loop structure, the sec insertion sequence (SECIS), that is necessary for the recognition of UGA as a Sec codon rather than as a stop signal. This protein shows highest expression in skeletal muscle and heart, and may be involved in oxidation-reduction reactions. A retroprocessed pseudogene, SEPW1P, has been identified and mapped to chromosome 1p35-34.
, selenoprotein W, 1
, selenoprotein W, muscle 1