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卵母细胞特异性因子结合小鼠透明带启动子活性所需的保守上游序列。

Oocyte-specific factors bind a conserved upstream sequence required for mouse zona pellucida promoter activity.

作者信息

Millar S E, Lader E, Liang L F, Dean J

机构信息

Laboratory of Cellular and Developmental Biology, National Institute of Diabetes and Digestive and Kidney Diseases, Bethesda, Maryland 20892.

出版信息

Mol Cell Biol. 1991 Dec;11(12):6197-204. doi: 10.1128/mcb.11.12.6197-6204.1991.

Abstract

The zona pellucida of mouse oocytes, composed of three major glycoproteins (ZP1, ZP2, and ZP3), performs crucial functions at fertilization and in early development. The transcripts encoding mouse ZP2 and ZP3 are coordinately expressed and accumulate in oocytes during a 2-week growth phase prior to ovulation. The 5'-flanking regions of mouse Zp-2 and Zp-3 genes and their human homologs contain five short DNA sequences (4 to 12 bp) that are 60 to 100% identical and are approximately equidistant upstream of the TATAA box in the four genes. Mutation of these five elements (I, IIA, IIB, III, and IV) in Zp-luciferase constructs demonstrates that the 12-bp element IV, positioned approximately 200 bp upstream from the TATAA box, is necessary for high-level expression from the mouse Zp-2 and Zp-3 promoters after microinjection into the nuclei of 50-microns-diameter oocytes. Injection of minimal Zp-3 promoter constructs containing element IV in either orientation also resulted in high levels of reporter gene activity, suggesting that the element is not only necessary but also sufficient for expression from zona pellucida promoters. Oligonucleotides containing the conserved element from either Zp-2 or Zp-3 form DNA-protein complexes of identical mobility in gel retardation assays using extracts of oocytes but not other tissues. These data are consistent with the hypothesis that common factors binding to conserved element IV are involved in coordinate expression of the oocyte-specific Zp-2 and Zp-3 zona pellucida genes.

摘要

小鼠卵母细胞的透明带由三种主要糖蛋白(ZP1、ZP2和ZP3)组成,在受精和早期发育过程中发挥着关键作用。编码小鼠ZP2和ZP3的转录本在排卵前2周的生长阶段在卵母细胞中协同表达并积累。小鼠Zp-2和Zp-3基因及其人类同源基因的5'侧翼区域包含五个短DNA序列(4至12个碱基对),它们的同源性为60%至100%,并且在这四个基因的TATAA框上游大致等距分布。Zp-荧光素酶构建体中这五个元件(I、IIA、IIB、III和IV)的突变表明,位于TATAA框上游约200个碱基对处的12个碱基对元件IV,对于将其显微注射到直径为50微米的卵母细胞核后从小鼠Zp-2和Zp-3启动子进行高水平表达是必需的。注射含有元件IV且方向任意的最小Zp-3启动子构建体也导致报告基因活性高水平,这表明该元件不仅对透明带启动子的表达是必需的,而且是充分的。在使用卵母细胞提取物而非其他组织提取物进行的凝胶阻滞试验中,含有来自Zp-2或Zp-3的保守元件的寡核苷酸形成迁移率相同的DNA-蛋白质复合物。这些数据与以下假设一致,即结合到保守元件IV的共同因子参与卵母细胞特异性透明带基因Zp-2和Zp-3的协同表达。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/831d/361804/ba7397a2401f/molcellb00036-0413-a.jpg

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