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鉴定和验证脂肪前体细胞增殖中新型 C/EBPβ 调控基因。

Identification and validation of novel C/EBPbeta-regulated genes in preadipocyte proliferation.

机构信息

Key Laboratory of Molecular Medicine, Ministry of Education, Department of Biochemistry and Molecular Biology, Fudan University Shanghai Medical College, Shanghai 200032, China.

出版信息

Chin Med J (Engl). 2010 May 5;123(9):1190-4.

Abstract

BACKGROUND

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.

METHODS

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.

RESULTS

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.

CONCLUSION

C/EBPbeta may regulate preadipocyte proliferation through activation of banp and trim35.

摘要

背景

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。

方法

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。

结果

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。

结论

C/EBPβ 可能通过激活 banp 和 trim35 来调节前脂肪细胞增殖。

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