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C/EBPε 通过内含子基质附着区序列参与全反式视黄酸诱导 U937 细胞中的 PI3Kγ。

C/EBPε participates in all-trans retinoic acid induction of PI3Kγ in U937 cells via an intronic matrix attachment region sequence.

机构信息

Department of Molecular and Cellular Biology, Institute of Medical Sciences, Shanghai Jiao Tong University School of Medicine, 280# Chongqing Road(S), Shanghai, 200025, People's Republic of China.

出版信息

Mol Biol Rep. 2010 Dec;37(8):3795-800. doi: 10.1007/s11033-010-0034-1. Epub 2010 Jul 27.

Abstract

ATRA (all-trans retinoic acid) regulates gene expression by binding as a ligand to its specific receptors like C/EBPε which is directly induced. In the U937 cell line, PI3Kγ is selectively induced over other PI3Ks by ATRA, although the mechanism is still unclear. Here, we show that C/EBPε and PI3Kγ are induced in U937 cells by ATRA both in levels of mRNA and protein. Reporter gene assay revealed that C/EBPε is able to interact with a previously identified 2 kb MAR (matrix attachment region) sequence in the last intron of PI3Kγ gene, and increases its linked heterogeneous reporter gene expression. ChIP assay showed that induction of endogenous PI3Kγ is at least partially caused by enhanced, direct C/EBPε binding to a 15 bp sequence at nucleotides 1428-1442 within this MAR sequence, and EMSA analysis confirmed this binding in vitro. The results above collectively show that C/EBPε participates in ATRA induction of PI3Kγ.

摘要

ATRA(全反式视黄酸)通过与其特定受体(如 C/EBPε)结合作为配体来调节基因表达,C/EBPε 被直接诱导。在 U937 细胞系中,ATRA 选择性地诱导 PI3Kγ 的表达,而不是其他 PI3Ks,尽管其机制尚不清楚。在这里,我们表明 ATRA 可在 U937 细胞中诱导 C/EBPε 和 PI3Kγ 的 mRNA 和蛋白水平表达。报告基因检测显示,C/EBPε 能够与 PI3Kγ 基因最后一个内含子中先前鉴定的 2 kb MAR(基质附着区)序列相互作用,并增加其连接的异源报告基因表达。ChIP 检测显示,内源性 PI3Kγ 的诱导至少部分是由于增强的、直接的 C/EBPε 结合到 MAR 序列中核苷酸 1428-1442 处的 15 个碱基对序列,EMSA 分析证实了这种体外结合。上述结果共同表明,C/EBPε 参与了 ATRA 诱导的 PI3Kγ 表达。

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