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CCAAT/增强子结合蛋白基因启动子:3T3-L1前脂肪细胞分化过程中核因子的结合

CCAAT/enhancer binding protein gene promoter: binding of nuclear factors during differentiation of 3T3-L1 preadipocytes.

作者信息

Christy R J, Kaestner K H, Geiman D E, Lane M D

机构信息

Department of Biological Chemistry, Johns Hopkins University School of Medicine, Baltimore, MD 21205.

出版信息

Proc Natl Acad Sci U S A. 1991 Mar 15;88(6):2593-7. doi: 10.1073/pnas.88.6.2593.

Abstract

Differentiation of 3T3-L1 preadipocytes into adipocytes is accompanied by increased expression of the nuclear protein C/EBP (CCAAT/enhancer binding protein) and by transcriptional activation of a group of adipose-specific genes. We report here the isolation of the murine C/EBP gene and the characterization of its promoter. Consistent with its proposed role in coordinating transcription during preadipocyte differentiation, an increase in the rate of transcription of the C/EBP gene precedes that of several adipose-specific genes whose promoters are transactivated by C/EBP. DNase I cleavage-inhibition patterns (footprinting) of the C/EBP gene promoter by nuclear factors from differentiated and undifferentiated 3T3-L1 cells identified two sites of differential factor binding. One site in the C/EBP gene promoter between nucleotides -252 and -239 binds a nuclear factor(s) present in preadipocytes that is lost or modified upon differentiation. Another site, between nucleotides -203 and -176, exhibits different but overlapping footprints by nuclear factors present in differentiated and undifferentiated cells. Gel retardation analysis with oligonucleotides corresponding to these sites revealed protein-oligonucleotide complexes containing these differentially expressed nuclear factors. The factor present in differentiated cells that binds at this site was identified as C/EBP (possibly in heterodimeric form with a homologous leucine-zipper protein), suggesting that C/EBP may regulate expression of its own gene.

摘要

3T3-L1前脂肪细胞向脂肪细胞的分化伴随着核蛋白C/EBP(CCAAT/增强子结合蛋白)表达的增加以及一组脂肪特异性基因的转录激活。我们在此报告小鼠C/EBP基因的分离及其启动子的特性。与其在协调前脂肪细胞分化过程中的转录作用一致,C/EBP基因转录速率的增加先于其启动子被C/EBP反式激活的几个脂肪特异性基因。来自分化和未分化的3T3-L1细胞的核因子对C/EBP基因启动子的DNase I切割抑制模式(足迹法)确定了两个差异因子结合位点。C/EBP基因启动子中核苷酸-252至-239之间的一个位点结合前脂肪细胞中存在的一种核因子,该因子在分化时丢失或发生改变。另一个位点在核苷酸-203至-176之间,分化和未分化细胞中存在的核因子显示出不同但重叠的足迹。用对应于这些位点的寡核苷酸进行凝胶阻滞分析,揭示了含有这些差异表达核因子的蛋白质-寡核苷酸复合物。在该位点结合的分化细胞中存在的因子被鉴定为C/EBP(可能与同源亮氨酸拉链蛋白形成异二聚体形式),这表明C/EBP可能调节其自身基因的表达。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf04/51279/b569fb203660/pnas01056-0568-a.jpg

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