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前强啡肽基因表达与核因子-κB因子相关。

Prodynorphin gene expression relates to NF-kappa B factors.

作者信息

Bakalkin G, Yakovleva T, Terenius L

机构信息

Department of Drug Dependence Research, Karolinska Institute, Stockholm, Sweden.

出版信息

Brain Res Mol Brain Res. 1994 Jul;24(1-4):301-12. doi: 10.1016/0169-328x(94)90143-0.

Abstract

The prodynorphin gene contains several kappa B motifs, suggesting that kappa B-specific DNA-binding factors may regulate its expression. Prodynorphin is known to be expressed in human tumor cell lines [Geiger et al., Regul. Peptides, 34 (1991) 181-188] and we report here that several DNA-binding factors of the NF-kappa B/c-Rel-family are present in the same cells. Three main kappa B-specific factors, presumably a p50 homodimer, NF-kappa B which is a p50/p65 heterodimer and a p65/c-Rel heterodimer were identified using an electromobility shift assay (EMSA), immunoabsorption and UV cross-linking experiments. Minor factors consisting of a novel kappa B-specific protein of about 125 kDa (p125) or being hetero-oligomeric, composed of p125 and either of three other subunits, namely p50, p65 and c-Rel, were also identified. The homo-oligomer of p125 may be identical to the kappa B-specific factor BETA, previously found only in brain [Korner et al., Neuron, 3 (1989) 563-572]. Comparison of prodynorphin mRNA levels with levels of the kappa B-specific DNA-binding factors revealed a negative correlation with the level of p50 homodimer, and a positive correlation with the ratio of the levels of p65/c-Rel to NF-kappa B. No association was found with proenkephalin mRNA levels which were significant in only one cell line. The p50 homodimer, but not p65/c-Rel and NF-kappa B, bound specifically to a DNA-motif within the dynorphin A-encoding gene sequence. This sequence is located in exon 4 and similar to the consensus kappa B-sequence. The dynorphin A-encoding sequence may represent an intragenic target for the p50 homodimer, which when bound to the sequence suppresses transcription.

摘要

强啡肽原基因包含几个κB基序,这表明κB特异性DNA结合因子可能调节其表达。已知强啡肽原在人类肿瘤细胞系中表达[盖格等人,《调节肽》,34(1991)181 - 188],我们在此报告,NF-κB/c-Rel家族的几种DNA结合因子存在于同一细胞中。使用电泳迁移率变动分析(EMSA)、免疫吸附和紫外线交联实验鉴定出三种主要的κB特异性因子,推测分别是p50同二聚体、作为p50/p65异二聚体的NF-κB和p65/c-Rel异二聚体。还鉴定出了由约125 kDa的新型κB特异性蛋白(p125)组成的次要因子,或者由p125与其他三个亚基(即p50、p65和c-Rel)之一组成的异源寡聚体。p125的同二聚体可能与先前仅在脑中发现的κB特异性因子BETA相同[科尔纳等人,《神经元》,3(1989)563 - 572]。将强啡肽原mRNA水平与κB特异性DNA结合因子的水平进行比较,发现与p50同二聚体水平呈负相关,与p65/c-Rel与NF-κB水平的比值呈正相关。未发现与脑啡肽原mRNA水平有相关性,脑啡肽原mRNA水平仅在一个细胞系中有显著差异。p50同二聚体而非p65/c-Rel和NF-κB特异性结合强啡肽A编码基因序列内的一个DNA基序。该序列位于外显子4中,与共有κB序列相似。强啡肽A编码序列可能代表p50同二聚体的基因内靶点,当与该序列结合时会抑制转录。

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