
IndraLab
Statements
isi
"Moreover, the results from co-immunoprecipitation (CO-IP), immunofluorescence and western blot assays showed that the physiological process due to USP26 interacted with AR and influenced AR deubiquitination, thus upregulating the proteins CCND1 and SPATA46 - which are associated with cell cycle progression and spermatogenesis - as well as decreasing the expression of TP73."
reach
"ChIP-qPCR of the promoters of Sox2, Nanog, Oct4, and Cbx7 in Usp26 differentiated ESCs on day 6 revealed binding of USP26, CBX4, CBX6, H2A-ubi1, and H3K27me3 to the Sox2, Nanog, and Cbx7 promoters, suggesting that promoter binding of these components led to a decrease in pluripotency gene expression."
isi
"Moreover, the results from co-immunoprecipitation (CO-IP), immunofluorescence and western blot assays showed that the physiological process due to USP26 interacted with AR and influenced AR deubiquitination, thus upregulating the proteins CCND1 and SPATA46 - which are associated with cell cycle progression and spermatogenesis - as well as decreasing the expression of TP73."
reach
"ChIP-qPCR of the promoters of Sox2, Nanog, Oct4, and Cbx7 in Usp26 differentiated ESCs on day 6 revealed binding of USP26, CBX4, CBX6, H2A-ubi1, and H3K27me3 to the Sox2, Nanog, and Cbx7 promoters, suggesting that promoter binding of these components led to a decrease in pluripotency gene expression."
reach
"ChIP-qPCR of the promoters of Sox2, Nanog, Oct4, and Cbx7 in Usp26 differentiated ESCs on day 6 revealed binding of USP26, CBX4, CBX6, H2A-ubi1, and H3K27me3 to the Sox2, Nanog, and Cbx7 promoters, suggesting that promoter binding of these components led to a decrease in pluripotency gene expression."
reach
"Examples include ubiquitin specific protease 10 (USP10), which can act on SMAD4 to make it deubiquitinated and stable, further promoting TGF-beta signaling [XREF_BIBR], and USP26, which promotes SMAD7 deubiquitination, thereby amplifying the inhibitory effect of SMAD7 and strengthening the inhibition of the TGF-beta signaling pathway [XREF_BIBR]."
| PMC
reach
"ChIP-qPCR of the promoters of Sox2, Nanog, Oct4, and Cbx7 in Usp26 differentiated ESCs on day 6 revealed binding of USP26, CBX4, CBX6, H2A-ubi1, and H3K27me3 to the Sox2, Nanog, and Cbx7 promoters, suggesting that promoter binding of these components led to a decrease in pluripotency gene expression."
sparser
"To understand how Usp26 expression is regulated, we assessed the promoter-binding activity of Usp26 by PRC1 subunits using the ChIP–qPCR assay during RA-induced ESC differentiation, and observed that PRC1 components PCGF2 and Cbx7 occupation as well as H2A-ubi1 modifications decreased significantly in Usp26 promoter (Supplementary Fig. xref d), thus indicating that CBX7 containing PRC1 complex is a potential repressor of Usp26 ."
sparser
"To understand how Usp26 expression is regulated, we assessed the promoter-binding activity of Usp26 by PRC1 subunits using the ChIP–qPCR assay during RA-induced ESC differentiation, and observed that PRC1 components PCGF2 and Cbx7 occupation as well as H2A-ubi1 modifications decreased significantly in Usp26 promoter (Supplementary Fig. xref d), thus indicating that CBX7 containing PRC1 complex is a potential repressor of Usp26 ."
USP26 affects cell differentiation
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7
reach
"ChIP-qPCR of the promoters of Sox2, Nanog, Oct4, and Cbx7 in Usp26 differentiated ESCs on day 6 revealed binding of USP26, CBX4, CBX6, H2A-ubi1, and H3K27me3 to the Sox2, Nanog, and Cbx7 promoters, suggesting that promoter binding of these components led to a decrease in pluripotency gene expression."
reach
"ChIP-qPCR of the promoters of Sox2, Nanog, Oct4, and Cbx7 in Usp26 differentiated ESCs on day 6 revealed binding of USP26, CBX4, CBX6, H2A-ubi1, and H3K27me3 to the Sox2, Nanog, and Cbx7 promoters, suggesting that promoter binding of these components led to a decrease in pluripotency gene expression."
USP26 affects homologous recombination
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6
USP26 activates homologous recombination.
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4
USP26 inhibits homologous recombination.
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2
reach
"To verify whether USP26 induction by TGF-beta is prevalent in other cell types, we analyzed the induction of USP26 and SMAD7 at early time points in the TGF-beta-responsive breast cancer cell lines MCF7, MDA-MB-231, T47D, and CAL51 and glioma cell lines U373, PCTC, and A172 (Fig XREF_FIG A-G)."
USP26 affects E7
4
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reach
"ChIP-qPCR of the promoters of Sox2, Nanog, Oct4, and Cbx7 in Usp26 differentiated ESCs on day 6 revealed binding of USP26, CBX4, CBX6, H2A-ubi1, and H3K27me3 to the Sox2, Nanog, and Cbx7 promoters, suggesting that promoter binding of these components led to a decrease in pluripotency gene expression."
reach
"ChIP-qPCR of the promoters of Sox2, Nanog, Oct4, and Cbx7 in Usp26 differentiated ESCs on day 6 revealed binding of USP26, CBX4, CBX6, H2A-ubi1, and H3K27me3 to the Sox2, Nanog, and Cbx7 promoters, suggesting that promoter binding of these components led to a decrease in pluripotency gene expression."
reach
"ChIP-qPCR of the promoters of Sox2, Nanog, Oct4, and Cbx7 in Usp26 differentiated ESCs on day 6 revealed binding of USP26, CBX4, CBX6, H2A-ubi1, and H3K27me3 to the Sox2, Nanog, and Cbx7 promoters, suggesting that promoter binding of these components led to a decrease in pluripotency gene expression."
E7 affects USP26
4
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reach
"ChIP-qPCR of the promoters of Sox2, Nanog, Oct4, and Cbx7 in Usp26 differentiated ESCs on day 6 revealed binding of USP26, CBX4, CBX6, H2A-ubi1, and H3K27me3 to the Sox2, Nanog, and Cbx7 promoters, suggesting that promoter binding of these components led to a decrease in pluripotency gene expression."
reach
"To understand how Usp26 expression is regulated, we assessed the promoter binding activity of Usp26 by PRC1 subunits using the ChIP-qPCR assay during RA induced ESC differentiation, and observed that PRC1 components PCGF2 and Cbx7 occupation as well as H2A-ubi1 modifications decreased significantly in Usp26 promoter, thus indicating that CBX7 containing PRC1 complex is a potential repressor of Usp26."
Reactive oxygen species affects USP26
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3
Reactive oxygen species inhibits USP26.
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2
Reactive oxygen species activates USP26.
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1
Reactive oxygen species activates USP26. 1 / 1
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1