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肝脏再生过程中Afr-2调控甲胎蛋白基因表达的序列要求。

Sequence requirements for Afr-2 regulation of alpha-fetoprotein gene expression during liver regeneration.

作者信息

Jin D K, Feuerman M H

机构信息

Department of Biochemistry, State University of New York, Brooklyn 11203, USA.

出版信息

Somat Cell Mol Genet. 1996 May;22(3):211-26. doi: 10.1007/BF02369911.

Abstract

Alpha-fetoprotein (AFP) gene expression occurs in the yolk sac, fetal liver and gut, and in the adult liver during regeneration and tumorigenesis. Polymorphism at a single genetic locus, Afr-2 (formerly known as Rif) between inbred mouse strains C3H/He and C57B1/6, results in different levels of AFP expression during liver regeneration. We examined AFP, histone H3, and albumin gene expression during liver regeneration and found that the strain-specific variance in AFP gene expression could not be attributed to a difference in the numbers of dividing cells. Experiments with transgenic mice revealed sequences required for Afr-2 regulation included 172 bp between -1010 and -838 bp and 118 bp immediately upstream of the AFP transcriptional start site-the same regions required for induction during liver regeneration. This suggests that the Afr-2 phenotype may stem from an allelic difference in a gene regulating gene expression during liver regeneration.

摘要

甲胎蛋白(AFP)基因表达发生于卵黄囊、胎儿肝脏和肠道,以及成体肝脏再生和肿瘤发生过程中。近交系小鼠C3H/He和C57B1/6之间在单个基因座Afr-2(以前称为Rif)存在多态性,导致肝脏再生期间AFP表达水平不同。我们检测了肝脏再生过程中甲胎蛋白、组蛋白H3和白蛋白基因的表达,发现AFP基因表达的品系特异性差异不能归因于分裂细胞数量的差异。转基因小鼠实验表明,Afr-2调控所需的序列包括-1010至-838 bp之间的172 bp以及AFP转录起始位点上游紧邻的118 bp,这与肝脏再生期间诱导所需的区域相同。这表明Afr-2表型可能源于肝脏再生期间调控基因表达的基因中的等位基因差异。

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