相关实验视频
Updated: Jul 27, 2025

14:01
Isolation and Derivation of Mouse Embryonic Germinal Cells
Published on: October 22, 2009
16.2K
这种突变首先会在怀孕8天的三/三小鼠胚胎中引起原始生殖细胞缺乏
Takayuki Sakurai1,2, Taisen Iguchi1, Kazuo Moriwaki3
1Graduate School of Integrated Science, Yokohama City University, Yokohama 236, Japan.
Development, growth & differentiation
|June 7, 2023
概括
这种突变会影响小鼠胚胎中原始生殖细胞 (PGC) 数量,大约发生性交后8.0天. 这表明ter基因对PGC的增殖和生存至关重要.
科学领域:
- 发育生物学是发展生物学.
- 遗传学 遗传学 是一个
- 生殖生物学 生殖生物学
背景情况:
- 已知ter (teratoma) 突变会导致原始生殖细胞 (PGC) 缺乏.
- 之前的研究观察到,在较晚的发育阶段 (性交后9.5-12.5天) 的特定小鼠菌株中存在这种缺陷.
研究的目的:
- 准确研究突变对PGC发育的影响.
- 为了确定由突变引起的PGC缺乏的确切时间和性质.
主要方法:
- 在先天C57BL/6J-ter小鼠胚胎 (性交后7.5-12.5天) 中分析PGC数量和分布.
- 使用聚合酶链反应 (PCR) 进行胚胎的基因定型,用于 Grl-1 locus 微卫星 DNA 多态化.
- 检查胚胎的完整序列切口.
主要成果:
- 在ter/ter和正常胚胎中,在性交后7.5天后,PGC数量与正常胚胎相似.
- 在ter/ter胚胎中的PGC数量并没有从共生后8.0-12.5天增加,与正常 littermates不同.
- PGC向生殖器脊的迁移没有受到影响;在异构合体 (+/ter) 和野生类型 (+/+) 胚胎之间没有观察到PGC数量差异.
结论:
- 这种突变不会影响PGC在性交后7.5天的最初出现.
- PGC缺乏症首先发生在性交后8.0天左右,与迁移和扩散的开始相吻合.
- 第三基因产物可能对PGC扩散或生存机制至关重要.
相关概念视频
Teratogenicity
2.5K
The ability of a drug to produce structural deformations and functional abnormalities in the developing embryo or the fetus is called teratogenicity, and the drug producing this effect is known as a teratogen. Teratogenic effects include stillbirth, miscarriage, intrauterine growth restriction, and neurocognitive delay. A teratogen may affect the embryo at different stages of development, which is important in determining the type and extent of the damage. During blastocyst formation, the early...
2.5K
In-vitro Mutagenesis
14.0K
To learn more about the function of a gene, researchers can observe what happens when the gene is inactivated or “knocked out,” by creating genetically engineered knockout animals. Knockout mice have been particularly useful as models for human diseases such as cancer, Parkinson’s disease, and diabetes.
14.0K

