Department of Animal Science, Texas A&M University, 2471 TAMU, College Station, TX 77843-2471, United States.
J Steroid Biochem Mol Biol. 2010 Oct;122(4):172-9. doi: 10.1016/j.jsbmb.2010.07.001. Epub 2010 Jul 17.
The A+U-rich binding factor 1 (AUF1 or HNRPD) gene produces predominant RNA binding proteins. The AUF1 transcript is alternatively spliced to produce four protein isoforms that stabilize or destabilize hundreds of mRNAs. Previously, we discovered that estradiol (E2) treatment of ovariectomized sheep increased concentrations of AUF1p45 protein which stabilized estrogen receptor alpha (ER) mRNA in the uterus. This study examined E2 regulation of AUF1 mRNAs in the sheep uterus. Northern analysis determined that E2 treatment increased concentrations of total AUF1 mRNAs twofold in endometrial and myometrial tissue compartments. In situ hybridization indicated that the increase was most intense in the glandular epithelium of endometrium. In a well characterized in vitro RNA stability assay, AUF1 3'UTR sequences were much more stable in uterine extracts from E2-treated ewes compared to extracts from control ewes. AUF1 mRNAs with alternative splicing of exons 2 and 7 (in the coding sequence) and exon 9 (in the 3'UTR) were identified. The only effect of E2 treatment on alternative splicing was that it reduced the percentage of AUF1 mRNAs containing exon 9-derived sequences. These data indicate that E2 up-regulates AUF1 and ER genes coordinately by a post-transcriptional mechanism.
富含 A+U 的结合因子 1(AUF1 或 HNRPD)基因产生主要的 RNA 结合蛋白。AUF1 转录本通过可变剪接产生四种蛋白异构体,这些异构体可以稳定或不稳定数百种 mRNA。以前,我们发现雌二醇(E2)处理去卵巢绵羊增加了 AUF1p45 蛋白的浓度,该蛋白稳定了子宫中的雌激素受体 alpha(ER)mRNA。本研究检查了 E2 对绵羊子宫中 AUF1 mRNA 的调节。Northern 分析确定,E2 处理使子宫内膜和子宫肌组织中总 AUF1 mRNA 的浓度增加了两倍。原位杂交表明,这种增加在子宫内膜的腺上皮中最为强烈。在一个特征明确的体外 RNA 稳定性测定中,与来自对照母羊的提取物相比,来自 E2 处理母羊的子宫提取物中 AUF1 3'UTR 序列更加稳定。鉴定出具有外显子 2 和 7(在编码序列中)和外显子 9(在 3'UTR 中)可变剪接的 AUF1 mRNAs。E2 处理对可变剪接的唯一影响是降低了包含外显子 9 衍生序列的 AUF1 mRNAs 的百分比。这些数据表明,E2 通过转录后机制协调地上调 AUF1 和 ER 基因。