A combined proteome and ultrastructural localization analysis of 14-3-3 proteins in transformed human amnion (AMA) cells

被引:21
|
作者
Moreira, Jose M. A. [1 ,2 ]
Shen, Tao [1 ,2 ,3 ]
Ohlsson, Gita [1 ,2 ]
Gromov, Pavel [1 ,2 ]
Gromova, Irina [1 ,2 ]
Celis, Julio E. [1 ,2 ]
机构
[1] Danish Canc Soc, Dept Prote Canc, Inst Canc Biol, DK-2100 Copenhagen O, Denmark
[2] Danish Canc Soc, Danish Ctr Translat Breast Canc Res DCTB, DK-2100 Copenhagen O, Denmark
[3] First Peoples Hosp Yunnan, Inst Basic Med Sci, Kunming 650032, Peoples R China
关键词
D O I
10.1074/mcp.M700439-MCP200
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The 14-3-3 proteins constitute a family of highly conserved and broadly expressed multifunctional polypeptides that are involved in a variety of important cellular processes that include cell cycle progression, growth, differentiation, and apoptosis. Although the exact cellular function(s) of 14-3-3 proteins is not fully elucidated, as a rule these proteins act by binding to protein ligands, thus regulating their activity; so far more than 300 cellular proteins have been reported to interact with 14-3-3 proteins. Binding to cognate interacting partners is isoform-specific, but redundancy also exists as several binding peptides can be recognized by all isoforms, and some functions can be carried out by any isoform indistinctly. Moreover by interacting with different ligands in a spatially and temporally regulated fashion the same isoform can play multiple possibly even opposing roles where the resultant cellular outcome will be determined by the integration of the various effects. Although there is a large body of literature on specific aspects of 14-3-3 biology, not much is known on the coordinated aspects of 14-3-3 isoform expression, post-translational modifications, and subcellular localization. To address the question of isoform-specific differences, we carried out a comparative analysis of the patterns of expression, phosphorylation, and subcellular localization of the 143-3-3, beta, epsilon, sigma, tau, and zeta protein isoforms in transformed human amnion (AMA) cells. To validate as well as broaden our observations we analyzed the occurrence of the various isoforms in a large number of established cell lines and mammary and urothelial tissue specimens. Given the systematic approach we undertook and our application of isoform-discriminating technologies to the analysis of various cellular systems, we expect the data presented in this study to serve as an enabling resource for researchers working with 14-3-3 proteins.
引用
收藏
页码:1225 / 1240
页数:16
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