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肝脏再生过程中甲胎蛋白基因表达的序列要求。

Sequence requirements for alpha-fetoprotein gene expression during liver regeneration.

作者信息

Lin Y, Jin D K, Vacher J, Feuerman M H

机构信息

Department of Biochemistry, State University of New York, Health Science Center at Brooklyn 11203, USA.

出版信息

Cell Growth Differ. 1995 Dec;6(12):1549-58.

PMID:9019160
Abstract

The alpha-fetoprotein (AFP) gene is expressed in fetal liver and in adult liver undergoing regeneration or tumorigenesis. It has been shown previously that three distal enhancers, a proximal promoter, and a dominant negative postnatal repressor element are required for the tissue-specific and developmental regulation of AFP gene expression. Using transgenic mice, we have determined the sequence requirements for AFP gene induction during liver regeneration. Two DNA sequences were found in all transgenes appropriately regulated in response to liver regeneration: a distal sequence between 1010 and 838 bp upstream of the structural gene and a proximal sequence within 118 bp of the transcriptional initiation site. In situ hybridization analysis showed that transgene expression during liver regeneration was first found in all hepatocytes and then localized to perinecrotic hepatocytes surrounding the central vein. This pattern of expression is reminiscent of that observed after birth for the transgenes, suggesting that repression of AFP gene expression after birth and liver injury may be regulated by similar mechanisms.

摘要

甲胎蛋白(AFP)基因在胎儿肝脏以及正在进行再生或发生肿瘤的成体肝脏中表达。先前已经表明,AFP基因表达的组织特异性和发育调控需要三个远端增强子、一个近端启动子和一个显性负性出生后抑制元件。利用转基因小鼠,我们确定了肝脏再生过程中AFP基因诱导的序列要求。在所有对肝脏再生有适当调控的转基因中发现了两个DNA序列:一个位于结构基因上游1010至838 bp之间的远端序列,以及一个位于转录起始位点118 bp内的近端序列。原位杂交分析表明,肝脏再生过程中的转基因表达首先在所有肝细胞中发现,然后定位于中央静脉周围的坏死周围肝细胞。这种表达模式让人想起出生后转基因所观察到的模式,表明出生后和肝脏损伤后AFP基因表达的抑制可能受相似机制调控。

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