现在是 2024年11月23日 周六 12点 中午好! 吃过午餐了吗?
- ATP发光检测
- 酶活性检测
- 乙酰胆碱酯酶AChE发光检测
- Calpain发光检测
- 二肽酶IV(DPPIV)发光检测
- GSH谷胱甘肽发光检测
- 磷酸二酯酶PDE检测
- 蛋白酶体Proteasome发光检测
- 分泌型碱性磷酸酶SEAP发光检测
- 激酶检测
- 去泛素化酶DUBs发光检测
- 应用发光细菌检测水质毒性
- 水母发光蛋白-钙离子检测
- 免疫化学发光检测
- 细胞凋亡检测
- 细胞增殖检测
- 荧光素酶检测
- 萤火虫荧光素酶检测
- 海肾荧光素酶检测
- Gaussia荧光素酶检测
- 双荧光素酶报告基因检测
- 双荧光素酶报告基因常见问题
- 荧光素酶报告基因常见问题
- 荧光素酶影响因素及注意事项
- DNA及RNA定量检测
- DNA定量检测
- RNA定量检测
- 支原体发光检测
- ADME药物代谢发光检测
- 单胺氧化酶AMO发光检测
- 细胞色素P450(CYP450)发光检测
- P糖蛋白P-GP发光检测
- 细胞毒性检测
- RNAi检测
- cAMP检测
- 干扰素的生物学活性检测
- 鲁米诺化学发光检测应用
- ATP法检测活性污泥生物活性
首页 > 所有下载 > 应用文献-Biological basis for restriction of microRNA targets to the 3′ untranslated region in mammalian mRNAs
应用文献-Biological basis for restriction of microRNA targets to the 3′ untranslated region in mammalian mRNAs
Biological basis for restriction of microRNA targets to the 3¢ untranslated region in mammalian mRNAs
Shuo Gu1, Lan Jin1, Feijie Zhang1, Peter Sarnow2 & Mark A Kay1 MicroRNAs (miRNAs) interact with target sites located in the 3¢ untranslated regions (3¢ UTRs) of mRNAs to downregulate their expression when the appropriate miRNA is bound to target mRNA. To establish the functional importance of target-site localization in the 3¢ UTR, we modified the stop codon to extend the coding region of the transgene reporter through the miRNA target sequence. As a result, the miRNAs lost their ability to inhibit translation but retained their ability to function as small interfering RNAs in mammalian cells in culture and in vivo. The addition of rare but not optimal codons upstream of the extended opening reading frame (ORF) made the miRNA target site more accessible and restored miRNA-induced translational knockdown. Taken together, these results suggest that active translation impedes miRNA-programmed RISC association with target mRNAs and support a mechanistic explanation for the localization of most miRNA target sites in noncoding regions of mRNAs in mammals. 查阅更多相关应用文章
|
- © 2010-2015 版权所有 | 原平皓生物
- 关于我们
- 联系我们
- 京ICP备10029779号-1