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参与小鼠精子受体基因mZP3卵母细胞特异性表达的顺式作用DNA元件位于该基因转录起始位点附近。

cis-acting DNA elements involved in oocyte-specific expression of mouse sperm receptor gene mZP3 are located close to the gene's transcription start site.

作者信息

Lira S A, Schickler M, Wassarman P M

机构信息

Department of Cell and Developmental Biology, Roche Institute of Molecular Biology, Roche Research Center, Nutley, NJ 07110.

出版信息

Mol Reprod Dev. 1993 Dec;36(4):494-9. doi: 10.1002/mrd.1080360414.

Abstract

We report that cis-acting DNA elements involved in oocyte-specific expression of the mouse sperm receptor gene (mZP3) are located close to the gene's transcription start site. Mice bearing a transgene that consists of only 153 nt of mZP3 5'-flanking region fused to the firefly luciferase gene (153-ZP3/LUC) expressed the reporter gene in ovary not in a wide variety of tissues; although two of three lines carrying 153-ZP3/LUC also expressed the transgene in forebrain and hypothalamus. Within the ovaries of transgenic mice, luciferase activity was restricted to growing oocytes. However, levels of luciferase activity in these oocytes were lower than those in oocytes from mice bearing transgenes that contain a larger segment of mZP3 5'-flanking region (470-6,500 nt) fused to the firefly luciferase gene. Mice bearing a transgene that consists of 470 nt of mZP3 5'-flanking region and mZP3 intragenic sequences (ZDT) were also analyzed. The presence of mZP3 intragenic sequences did not result in significantly increased levels of firefly luciferase activity in oocytes of mice carrying the ZDT transgene. Overall, these results suggest that as little as 153 nt of mZP3 5'-flanking region is sufficient to target expression of the firefly luciferase gene to mouse oocytes and that the mZP3 intragenic sequences probably do not contain enhancer elements. Rather, enhancer elements are probably present between-153 and -470 nt of the mZP3 5'-flanking region.

摘要

我们报告称,参与小鼠精子受体基因(mZP3)卵母细胞特异性表达的顺式作用DNA元件位于该基因转录起始位点附近。携带仅由153个核苷酸的mZP3 5'侧翼区域与萤火虫荧光素酶基因融合而成的转基因(153-ZP3/LUC)的小鼠,在卵巢而非多种组织中表达报告基因;尽管携带153-ZP3/LUC的三个品系中有两个也在前脑和下丘脑表达转基因。在转基因小鼠的卵巢内,荧光素酶活性仅限于生长中的卵母细胞。然而,这些卵母细胞中的荧光素酶活性水平低于携带包含更大片段mZP3 5'侧翼区域(470 - 6500个核苷酸)与萤火虫荧光素酶基因融合的转基因小鼠的卵母细胞中的活性水平。还分析了携带由470个核苷酸的mZP3 5'侧翼区域和mZP3基因内序列组成的转基因(ZDT)的小鼠。mZP3基因内序列的存在并未导致携带ZDT转基因的小鼠卵母细胞中萤火虫荧光素酶活性水平显著增加。总体而言,这些结果表明,仅153个核苷酸的mZP3 5'侧翼区域就足以将萤火虫荧光素酶基因的表达靶向小鼠卵母细胞,并且mZP3基因内序列可能不包含增强子元件。相反,增强子元件可能存在于mZP3 5'侧翼区域的-153至-470个核苷酸之间。

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