Chamboredon Sandrine, Castellazzi Marc
Unité de Virologie Humaine, INSERM-U412, Ecole Normale Supérieure, IFR128 BioSciences Lyon-Gerland, 46 allée d'Italie, 69364 Lyon Cedex 07, France.
Oncogene. 2005 Apr 7;24(15):2547-57. doi: 10.1038/sj.onc.1208489.
Transformation of chick embryo fibroblasts (CEFs) by the v-Jun oncoprotein correlates with a downregulation of the alpha 2 (I) collagen gene. To investigate whether this gene constitutes a direct target of v-Jun, an analysis of a large proximal fragment of the promoter, extending from position -1080 to +109, was performed. Transient transfections with -1080/+109 and deleted derivatives revealed that a short proximal fragment, -433/+11, is the target for repression by v-Jun. Extensive analysis, conducted in CEFs and in Sp1/3-deficient Drosophila SL2 cells, further showed that (i) high constitutive activity of -433/+11 requires a direct binding of the ubiquitous Sp1 and/or Sp3 transcription factors acting on two distinct motifs, that is, a proximal TCC-rich region and an upstream GC box, and that (ii) repression by v-Jun does not require any direct binding of the oncoprotein to the DNA, but an indirect binding within a v-Jun-Sp1/3-DNA chromatin-associated complex. This situation is reminiscent of a situation previously reported with the tata-less, SPARC (secreted protein, acidic, and rich in cysteine) target promoter that regulates the expression of another extracellular matrix component in the same model of cell transformation. Taken together, these data reinforce the view that, at least in CEFs, v-Jun downregulates a family of direct target genes by binding to the DNA indirectly through Sp1/3.
v-Jun癌蛋白对鸡胚成纤维细胞(CEF)的转化与α2(I)胶原蛋白基因的下调相关。为了研究该基因是否构成v-Jun的直接靶标,我们对启动子的一个大的近端片段进行了分析,该片段从-1080位延伸至+109位。用-1080/+109及其缺失衍生物进行瞬时转染,结果显示一个短的近端片段-433/+11是v-Jun抑制的靶标。在CEF和Sp1/3缺陷的果蝇SL2细胞中进行的广泛分析进一步表明:(i)-433/+11的高组成活性需要普遍存在的Sp1和/或Sp3转录因子直接结合到两个不同的基序上,即近端富含TCC的区域和上游GC盒;(ii)v-Jun的抑制作用不需要癌蛋白与DNA直接结合,而是通过v-Jun-Sp1/3-DNA染色质相关复合物进行间接结合。这种情况让人联想到之前报道的无TATA盒的SPARC(分泌蛋白,酸性且富含半胱氨酸)靶启动子的情况,该启动子在相同的细胞转化模型中调节另一种细胞外基质成分的表达。综上所述,这些数据强化了这样一种观点,即至少在CEF中,v-Jun通过与Sp1/3间接结合到DNA上来下调一系列直接靶基因。