Key Laboratory of Molecular Medicine, Ministry of Education, Department of Biochemistry and Molecular Biology, Fudan University Shanghai Medical College, Shanghai 200032, China.
Chin Med J (Engl). 2010 May 5;123(9):1190-4.
CCAAT/enhancer-binding protein beta (C/EBPbeta) is required for mitotic clonal expansion (MCE) during adipogenesis. It is still unclear how C/EBPbeta regulates MCE in the earlier differentiation programs of 3T3-L1 preadipocytes. The purpose of this paper was to understand why C/EBPbeta is required for preadipocyte proliferation, and identify new target genes of C/EBPbeta with chromatin immunoprecipitation (ChIP)-on-chip.
Postconfluent growth-arrested 3T3-L1 preadipocytes were induced to differentiation using a standard differentiation protocol. ChIP was performed at 20 hours after induction with specific anti-C/EBPbeta antibodies. The precipitated DNA was amplified, labeled and hybridized with a mouse promoter microarray. Compared with the control in which the ChIP experiment was performed with non-specific antibody, only the genes with a signal increasing more than 2 fold were considered as candidate genes.
A total of 110 candidate genes were identified. BTG3 associated nuclear protein (SMAR1, Banp) and tripartite motif-containing 35 (Hls5, trim35) were two target genes among the 110 candidate genes which are involved in cell cycle regulation; the binding of C/EBPbeta to the promoter of banp and trim35 was verified by ChIP-PCR.
C/EBPbeta may regulate preadipocyte proliferation through activation of banp and trim35.
CCAAT/增强子结合蛋白β(C/EBPβ)是脂肪生成过程中有丝分裂克隆扩张(MCE)所必需的。目前尚不清楚 C/EBPβ 如何调节 3T3-L1 前脂肪细胞早期分化程序中的 MCE。本文旨在了解为什么 C/EBPβ 是前脂肪细胞增殖所必需的,并通过染色质免疫沉淀(ChIP)-芯片鉴定 C/EBPβ 的新靶基因。
将生长停滞的 3T3-L1 前脂肪细胞用标准分化方案诱导分化。诱导后 20 小时用特异性抗 C/EBPβ 抗体进行 ChIP。沉淀的 DNA 被扩增、标记并与小鼠启动子微阵列杂交。与用非特异性抗体进行 ChIP 实验的对照相比,只有信号增加超过 2 倍的基因才被认为是候选基因。
共鉴定出 110 个候选基因。BTG3 相关核蛋白(SMAR1,Banp)和三肽基含 35(Hls5,Trim35)是 110 个候选基因中的两个靶基因,它们参与细胞周期调节;通过 ChIP-PCR 验证了 C/EBPβ 与 banp 和 trim35 启动子的结合。
C/EBPβ 可能通过激活 banp 和 trim35 来调节前脂肪细胞增殖。