Tang Q Q, Jiang M S, Lane M D
Department of Biological Chemistry, The Johns Hopkins University School of Medicine, Baltimore, Maryland 21205, USA.
Mol Cell Biol. 1999 Jul;19(7):4855-65. doi: 10.1128/MCB.19.7.4855.
Expression of C/EBPalpha is required for differentiation of 3T3-L1 preadipocytes into adipocytes. Previous investigations indicated that transcription of the C/EBPalpha gene is sequentially activated during differentiation, initially by C/EBPbeta and C/EBPdelta and later by C/EBPalpha (autoactivation). These events are mediated by a C/EBP regulatory element in the promoter of the C/EBPalpha gene. This article presents evidence that members of the Sp family, notably Sp1, act repressively on the C/EBPalpha promoter prior to the induction of differentiation. Sp1 was shown to bind to a GC box at the 5' end of the C/EBP regulatory element in the C/EBPalpha promoter and, in so doing, to competitively prevent binding to and transactivation of the promoter by the C/EBPs. One of the differentiation inducers methylisobutylxanthine (a cAMP phosphodiesterase inhibitor) or Forskolin, both of which increase the cellular cAMP level, causes down-regulation of Sp1. This decrease in Sp1 level early in the differentiation program appears to facilitate access of C/EBPbeta and/or C/EBPdelta to the C/EBP regulatory element and, thereby, derepression of the C/EBPalpha gene.
C/EBPα 的表达是 3T3-L1 前脂肪细胞分化为脂肪细胞所必需的。先前的研究表明,C/EBPα 基因的转录在分化过程中被依次激活,最初由 C/EBPβ 和 C/EBPδ 激活,随后由 C/EBPα(自激活)激活。这些事件由 C/EBPα 基因启动子中的一个 C/EBP 调控元件介导。本文提供的证据表明,Sp 家族成员,尤其是 Sp1,在分化诱导之前对 C/EBPα 启动子起抑制作用。Sp1 被证明与 C/EBPα 启动子中 C/EBP 调控元件 5' 端的一个 GC 盒结合,这样做会竞争性地阻止 C/EBPs 与启动子结合并对其进行反式激活。分化诱导剂之一甲基异丁基黄嘌呤(一种 cAMP 磷酸二酯酶抑制剂)或福斯可林,两者都会提高细胞内 cAMP 水平,导致 Sp1 下调。在分化程序早期 Sp1 水平的这种降低似乎有助于 C/EBPβ 和/或 C/EBPδ 进入 C/EBP 调控元件,从而使 C/EBPα 基因去抑制。