抑制因子
SMAD公司
染色质免疫沉淀
心理压抑
Smad2蛋白
发起人
基因表达调控
生物
细胞生物学
基因
下调和上调
分子生物学
化学
信号转导
基因表达
遗传学
作者
Marco A. Briones‐Orta,Marcela Sosa‐Garrocho,Paola Moreno‐Alvarez,Miguel A. Fonseca-Sánchez,Marina Macı́as-Silva
标识
DOI:10.1016/j.bbrc.2006.01.041
摘要
SnoN and Ski oncoproteins are co-repressors for Smad proteins and repress TGF-β-responsive gene expression. The smad7 gene is a TGF-β target induced by Smad signaling, and its promoter contains the Smad-binding element (SBE) required for a positive regulation by the TGF-β/Smad pathway. SnoN and Ski co-repressors also bind SBE but regulate negatively smad7 gene. Ski along with Smad4 binds and represses the smad7 promoter, whereas the repression mechanism by SnoN is not clear. Ski and SnoN overexpression inhibits smad7 reporter expression induced through TGF-β signaling. Using chromatin immunoprecipitation assays, we found that SnoN binds smad7 promoter at the basal condition, whereas after a short TGF-β treatment for 15-30 min SnoN is downregulated and no longer bound smad7 promoter. Interestingly, after a prolonged TGF-β treatment SnoN is upregulated and returns to its position on the smad7 promoter, functioning probably as a negative feedback control. Thus, SnoN also seems to regulate negatively the TGF-β-responsive smad7 gene by binding and repressing its promoter in a similar way to Ski.
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