摘要
目的:研究蛋白激酶B(PKB)的活性变化对小鼠受精卵早期发育的影响。方法:将野生型、持续激活型和激酶失活型PKB克隆至pBluescriptII/SK表达载体中,体外转录成mRNA,显微注射到1-细胞期受精卵中,观察受精卵分裂情况。结果:1-细胞期受精卵注射野生型或持续激活型PKB的mRNA后,卵裂率均增加,而持续激活型PKB的促进作用更为显著;相反注射激酶失活型PKB的mRNA后,卵裂率明显降低。结论:PKB能促进小鼠1-细胞期受精卵的发育,其活化对于小鼠受精卵的发育是必需的。
Objective: To investigate the effect of protein kinase B(PKB) on the regulation of mouse early embryo development. Methods: Wild type, constitutively active and kinase dead PKB(PKB-KD) were cloned and inserted into the vector pBluescript II/SK, transcribed into mRNA in vitro and then microinjected into mouse 1-cell stage fertilized eggs to observe the mitotic division of eggs. Results: Injection of mRNA coding for a constitutively active PKB(myr-PKB) into 1-cell stage fertilized eggs induced cell division more effectively than injection of wild type PKB(PKB-WT) mRNA, whereas microinjection ofmRNA of PKB-KD delayed the first mitotic division. Conclusion: PKB can promote the division of mouse 1-cell stage fertilized eggs. The activation of this kinase is necessary for the first round mitosis of mouse embryos.
出处
《生殖与避孕》
CAS
CSCD
北大核心
2007年第10期633-638,共6页
Reproduction and Contraception
基金
国家自然科学基金项目(30570945)资助
关键词
小鼠受精卵
蛋白激酶B(PKB)
定点突变
mouse fertilized eggs
protein kinase B(PKB)
site-directed mutagenesis