Protein kinase B/Akt may regulate G2/M transition in the fertilized mouse egg by changing the localization of p21Cip1/WAF1
Protein kinase B/Akt may regulate G2/M transition in the fertilized mouse egg by changing the localization of p21Cip1/WAF1
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DOI:
10.1002/cbf.1743
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发表时间:
2011-06
影响因子:
3.6
通讯作者:
Di-di Wu;C. Feng;Xiao‐yan Xu;Jian-ying Xiao;Chao Liu;J. Meng;E. Wang;Bing‐zhi Yu
中科院分区:
文献类型:
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作者:
Di-di Wu;C. Feng;Xiao‐yan Xu;Jian-ying Xiao;Chao Liu;J. Meng;E. Wang;Bing‐zhi Yu
Protein kinase B (PKB, also called Akt) is known as a serine/threonine protein kinase. Some studies indicate that the Akt signalling pathway strongly promotes G2/M transition in mammalian cell cycle progression, but the mechanism remains to be clarified, especially in the fertilized mouse egg. Here, we report that the expression of Akt at both the protein and mRNA level was highest in G2 phase, accompanied by a peak of Akt activity. In addition, the subcellular localization of p21Cip1/WAF1 has been proposed to be critical in the cell cycle. Hence, we detected the expression and localization of p21Cip1/WAF1 after injecting fertilized mouse eggs with Akt mRNA. In one‐cell stage fertilized embryos microinjected with mRNA coding for a constitutively active myristoylated Akt (myr‐Akt), p21Cip1/WAF1 was retained in the cytoplasm. Microinjection of mRNA of kinase‐deficient Akt(Akt‐KD) resulted in nuclear localization of p21Cip1/WAF1. Meanwhile, microinjection of different types of Akt mRNA affected the phosphorylation status of p21Cip1/WAF1. However, there was no obvious difference in the protein expression of p21Cip1/WAF1. Therefore, Akt controls the cell cycle by changing the subcellular localization of p21Cip1/WAF1, most likely by affecting the phosphorylation status of p21Cip1/WAF1. Copyright © 2011 John Wiley & Sons, Ltd.