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年轻和老年小鼠子宫中雌激素靶基因的转录谱分析。

Transcription profiling of estrogen target genes in young and old mouse uterus.

作者信息

Khalyfa Abdelnaby, Klinge Carolyn M, Hall William C, Zhao Xuechun, Miller Marilyn M, Wang Eugenia

机构信息

Department of Biochemistry and Molecular Biology, University of Louisville School of Medicine, 570 South Preson St Baxter Building RM. 304, Louisville, KY 40292, USA.

出版信息

Exp Gerontol. 2003 Oct;38(10):1087-99. doi: 10.1016/s0531-5565(03)00210-9.

Abstract

The goal of this study was to identify age-related changes in the expression of estrogen target genes in mouse uterus. We developed a novel 'estrogen response element (ERE) Chip' microarray bearing 297 genes including both known estrogen target genes and genes identified by searching the mouse genome database to have EREs, AP-1 sites, and Sp1 sites, all targets of estrogen receptor (ER) regulation. 400-500 bp PCR products of these 297 genes were printed onto nylon membranes creating the 'ERE Chip' microarray. This microarray is unique because it is the first estrogen-responsive gene-specific microarray to identify changes in uterine gene expression in young versus old mice. Using this ERE microarray we identified 10 uterine genes whose expression was up-regulated in old mice, e.g. beta-actin, calcium binding protein 45a, Sp1, and COUP-TFII. In contrast, the expression of only 4 uterine genes, i.e., complement C3, lactoferrin, Muc-1, and 17-beta-hydroxysteroid dehydrogenase 8 (H2-Ke6) was down-regulated in old mice. These changes may reflect an increase in stromal and a decrease in glandular epithelial gene expression, and may be associated with age-related changes in these tissue compartments within the uterus, possibly leading to the decline in reproductive function in C57Bl/6 mice.

摘要

本研究的目的是确定小鼠子宫中雌激素靶基因表达的年龄相关变化。我们开发了一种新型的“雌激素反应元件(ERE)芯片”微阵列,其上载有297个基因,包括已知的雌激素靶基因以及通过搜索小鼠基因组数据库确定具有ERE、AP-1位点和Sp1位点的基因,这些都是雌激素受体(ER)调控的所有靶点。将这297个基因的400 - 500 bp PCR产物打印到尼龙膜上,制成“ERE芯片”微阵列。这种微阵列是独一无二的,因为它是首个用于识别年轻与年老小鼠子宫基因表达变化的雌激素反应基因特异性微阵列。利用这个ERE微阵列,我们鉴定出10个在年老小鼠中表达上调的子宫基因,例如β-肌动蛋白、钙结合蛋白45a、Sp1和COUP-TFII。相比之下,只有4个子宫基因,即补体C3、乳铁蛋白、Muc-1和17-β-羟基类固醇脱氢酶8(H2-Ke6)在年老小鼠中的表达下调。这些变化可能反映了基质中基因表达的增加和腺上皮基因表达的减少,并且可能与子宫内这些组织区室的年龄相关变化有关,这可能导致C57Bl/6小鼠生殖功能的下降。

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