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染色质免疫沉淀分析显示,CREB 和丝氨酸 133 磷酸化 CREB 结合到 CART 基因近端启动子上。

Chromatin immunoprecipitation assays revealed CREB and serine 133 phospho-CREB binding to the CART gene proximal promoter.

机构信息

Yerkes National Research Primate Center of Emory University, Atlanta, GA 30329, USA.

出版信息

Brain Res. 2010 Jul 16;1344:1-12. doi: 10.1016/j.brainres.2010.04.069. Epub 2010 May 6.

Abstract

Both over expression of cyclic AMP response element binding protein (CREB) in the nucleus accumbens (NAc), and intra-accumbal injection of cocaine- and amphetamine-regulated transcript (CART) peptides, have been shown to decrease cocaine reward. Also, over expression of CREB in the rat NAc increased CART mRNA and peptide levels, but it is not known if this was due to a direct action of P-CREB on the CART gene promoter. The goal of this study was to test if CREB and P-CREB bound directly to the CRE site in the CART promoter, using chromatin immunoprecipitation (ChIP) assays. ChIP assay with anti-CREB antibodies showed an enrichment of the CART promoter fragment containing the CRE region over IgG precipitated material, a non-specific control. Forskolin, which was known to increase CART mRNA levels in GH3 cells, was utilized to show that the drug increased levels of P-CREB protein and P-CREB binding to the CART promoter CRE-containing region. A region of the c-Fos promoter containing a CRE cis-regulatory element was previously shown to bind P-CREB, and it was used here as a positive control. These data suggest that the effects of CREB over expression on blunting cocaine reward could be, at least in part, attributed to the increased expression of the CART gene by direct interaction of P-CREB with the CART promoter CRE site, rather than by some indirect action.

摘要

无论是在伏隔核(NAc)核内过度表达环磷酸腺苷反应元件结合蛋白(CREB),还是在 NAc 内注射可卡因和安非他命调节转录物(CART)肽,都已被证明可降低可卡因的奖赏作用。此外,CREB 在大鼠 NAc 中的过度表达增加了 CART mRNA 和肽水平,但尚不清楚这是否是由于 P-CREB 对 CART 基因启动子的直接作用。本研究的目的是使用染色质免疫沉淀(ChIP)测定来测试 CREB 和 P-CREB 是否直接与 CART 启动子中的 CRE 位点结合。用抗 CREB 抗体进行的 ChIP 测定显示,在 IgG 沉淀物质(非特异性对照)上,含有 CRE 区域的 CART 启动子片段被富集。众所周知,forskolin 可增加 GH3 细胞中的 CART mRNA 水平,本研究利用它来表明该药物增加了 P-CREB 蛋白的水平以及 P-CREB 与 CART 启动子 CRE 富含区域的结合。先前已显示 c-Fos 启动子的一个含有 CRE 顺式调节元件的区域与 P-CREB 结合,在此将其用作阳性对照。这些数据表明,CREB 过表达对可卡因奖赏作用减弱的影响至少部分归因于 P-CREB 与 CART 启动子 CRE 位点的直接相互作用导致 CART 基因表达增加,而不是通过某种间接作用。

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