sp3111 RNAi转基因小鼠模型的评价以及sp3111下调表达对受精及早胚发育的影响

doi:10.3969/j.issn.1674-5817.2011.02.002

实验动物与比较医学 ›› 2011, Vol. 31 ›› Issue (2): 83-86.DOI: 10.3969/j.issn.1674-5817.2011.02.002

sp3111 RNAi转基因小鼠模型的评价以及sp3111下调表达对受精及早胚发育的影响

华叶¹, 贾晓峰², 华敏敏³, 袁瑶², 范立强¹, 施惠娟²

1.华东理工大学生物工程学院,上海 200237;
2.上海市计划生育科学研究所国家人口计生委计划生育药具重点实验室,上海 200032;
3.中科院上海生命科学研究院生化细胞所,上海 200031

收稿日期:2010-10-21 出版日期:2011-04-25 发布日期:2011-04-25
作者简介:华叶(1983-), 女,硕士研究生,从事生物化学分子生物学研究,E-mail:taq1999@163.com
基金资助:
国家自然科学基金(30571968)资助

Evaluation of Sp3111 RNAi Transgenic Mice Model and Outcome of in vitro Fertilization with Spermatozoa from Sp3111 RNAi Transgenic Mice

HUA Ye¹, JIA Xiao-feng², HUA Min-min³, YUAN Yao², FAN Li-qiang¹, SHI Hui-juan²

1. Biological Engineering College,East China University of Science and Technology, Shanghai 200237, China;
2. NPFPC Key Laboratory of Contraceptives and Devices, Shanghai Institute of Planned Parenthood Research, Shanghai 200032,China;
3. Institute of Biochemistry and Cell Biology,SIBS,CAS, Shanghai 200031,China

Received:2010-10-21 Online:2011-04-25 Published:2011-04-25

摘要/Abstract

摘要： 目的评价sp3111 RNAi转基因小鼠模型的应用价值以及探讨SP3111蛋白降低表达对受精及早期胚胎发育的影响。方法 ①采用Real-Time PCR方法分别检测F1代和F4代转基因RNAi小鼠中sp3111 mRNA的表达变化,并比较2代间干扰效率的差异。②将精子分为实验组(F4代小鼠精子组)和对照组(野生小鼠精子组),进行体外授精实验,观察受精率及碎裂胚胎的发生率。结果 ①F1代和F4代小鼠中干扰效率的差异无统计学意义(P>0.05)。②实验组的正常胚胎与碎裂胚胎的形成率分别为34.48%和46.21%,与对照组相比均有显著差异(P<0.05)。结论 ①RNAi转基因小鼠中RNAi诱导的转录沉默可稳定遗传至F4代。②SP3111下调表达对小鼠受精及早期胚胎发育有明显的影响。

关键词: 转基因RNAi小鼠, 多代遗传, 体外授精实验, Real-Time PCR

Abstract: Objective To evaluate application value of Sp3111 RNAi transgenic mice model and to study the function of the sp3111 protein in fertilization and early embryo development. Methods ①real-time quantitative PCR was used to analysis the expression of sp3111 mRNA both in F1 and F4 generation, and comparing the suppression efficiency of RNAi between the two generations. ②Sperm samples collected from male Sp3111 RNAi transgenic mice(F4 generation) and from wild type mice as control group followed by IVF. The two groups were observed for the rates of fertilization and embryo fragmentation. Results ①No significant difference was found between F1 and F4 generation in suppression efficiency of RNAi PŁľ0.05. ②The rates of normal and fragmented embryos of the experimental group were 34.48% and 46.21%, respectively,significantly different from those of the control group (P<0.05). Conclusion ①the suppression efficiency of RNAi in Sp3111 RNAi transgenic mice could be transmitted stably to F4 generation. ②The low expression of sp3111 gene remarkably affected fertilization and early embryo development in mice.

Key words: Transgenic RNAi mice, Genetic stability, In vitro fertilization, Real-Time PCR

中图分类号:

Q95-33

华叶, 贾晓峰, 华敏敏, 袁瑶, 范立强, 施惠娟. sp3111 RNAi转基因小鼠模型的评价以及sp3111下调表达对受精及早胚发育的影响[J]. 实验动物与比较医学, 2011, 31(2): 83-86.

HUA Ye, JIA Xiao-feng, HUA Min-min, YUAN Yao, FAN Li-qiang, SHI Hui-juan. Evaluation of Sp3111 RNAi Transgenic Mice Model and Outcome of in vitro Fertilization with Spermatozoa from Sp3111 RNAi Transgenic Mice[J]. Laboratory Animal and Comparative Medicine, 2011, 31(2): 83-86.

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sp3111 RNAi转基因小鼠模型的评价以及sp3111下调表达对受精及早胚发育的影响

Evaluation of Sp3111 RNAi Transgenic Mice Model and Outcome of in vitro Fertilization with Spermatozoa from Sp3111 RNAi Transgenic Mice

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