14-3-3 Gene expression in regenerating rat liver after 2/3 partial hepatectomy

被引:5
|
作者
Xue, D. M. [1 ,2 ]
Guo, X. Q. [1 ,2 ]
Chen, R. [1 ,2 ]
Niu, Z. P. [1 ,2 ]
Xu, C. S. [1 ,2 ]
机构
[1] Henan Normal Univ, Coll Life Sci, Xinxiang, Henan, Peoples R China
[2] Key Lab Cell Differentiat Regulat, Xinxiang, Henan, Peoples R China
关键词
14-3-3; mRNA; Liver regeneration; Reverse transcription-polymerase chain reaction; DNA-DAMAGE; STEM-CELLS; PHOSPHATASE; CANCER; PROGRESSION; BINDING; CDC25;
D O I
10.4238/2015.March.20.12
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
14-3-3 Proteins are a ubiquitous family of molecules that participate in protein kinase signaling pathways in all eukaryotic cells. Functioning as phosphoserine/phosphothreonine-binding modules, 14-3-3 proteins participate in the phosphorylation-dependent protein-protein interactions that control progression through the cell cycle, initiation and maintenance of DNA damage checkpoints, activation of MAP kinases, prevention of apoptosis, and coordination of integrin signaling and cytoskeletal dynamics. During liver regeneration after partial hepatectomy, normally quiescent hepatocytes undergo hypertrophy and proliferation to restore the liver mass. In this study, we investigated the expression patterns of 14-3-3 mRNAs in regenerating rat liver after 2/3 partial hepatectomy using real-time quantitative reverse transcription-polymerase chain reaction. All mRNAs of the 14-3-3 7 isotypes were expressed at 10 time points. Upregulation of 14-3-3 xi mRNA expression and downregulation of 14-3-3 sigma mRNA expression from 0 to 6 h may play important roles in the entry into S-phase. Downregulation of 14-3-3 beta, gamma, sigma, eta, and tau mRNA expression from 24 to 30 h, when compared to 0 h, was closely related to entry into mitosis.
引用
收藏
页码:2023 / 2030
页数:8
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