Deja vu in proteomics. A hit parade of repeatedly identified differentially expressed proteins

被引:286
作者
Petrak, Jiri [1 ,2 ]
Ivanek, Robert [3 ]
Toman, Ondrej [1 ]
Cmejla, Radek [1 ]
Cmejlova, Jana [1 ]
Vyoral, Daniel [1 ]
Zivny, Jan [2 ]
Vulpe, Christopher D.
机构
[1] Inst Hematol & Blood Transfus, CR-12820 Prague, Czech Republic
[2] Charles Univ Prague, Fac Med 1, Dept Pathophysiol, Prague, Czech Republic
[3] Acad Sci Czech Republ, Inst Mol Genet, Prague, Czech Republic
关键词
2-D PAGE; differential expression; enolase; meta-analysis; most abundant;
D O I
10.1002/pmic.200700919
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
After reading many 2-DE-based articles featuring lists of the differentially expressed proteins, one starts experiencing a disturbing deja vu. The same proteins seem to predominate regardless of the experiment, tissue or species. To quantify the occurrence of individual differentially expressed proteins in 2-DE experiment reports, we compiled the identities of differentially expressed proteins identified in human, mouse, and rat tissues published in three recent volumes of Proteomics and calculated the appearance of the most predominant proteins in the dataset. The most frequently identified protein is a highly abundant glycolytic enzyme enolase 1, differentially expressed in nearly every third experiment on both human and rodent tissues. Heat-shock protein 27 (HSP27) and heat-shock protein 60 (HSP60) were differentially expressed in about 30 percent of human and rodent samples, respectively. Considering protein families as units, keratins and peroxiredoxins are the most frequently identified molecules, with at least one member of the group being differentially expressed in about 40 percent of all experiments. We suggest that the frequent identification of these proteins must be considered in the interpretation of any 2-DE studies. We consider if these commonly observed changes represent common cellular stress responses or are a reflection of the technical limitations of 2-DE.
引用
收藏
页码:1744 / 1749
页数:6
相关论文
共 16 条
[1]   NONNEURONAL ENOLASE IS AN ENDOTHELIAL HYPOXIC STRESS PROTEIN [J].
AARONSON, RM ;
GRAVEN, KK ;
TUCCI, M ;
MCDONALD, RJ ;
FARBER, HW .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (46) :27752-27757
[2]   ENO1 gene product binds to the c-myc promoter and acts as a transcriptional repressor:: relationship with Myc promoter-binding protein 1 (MBP-1) [J].
Feo, S ;
Arcuri, D ;
Piddini, E ;
Passantino, R ;
Giallongo, A .
FEBS LETTERS, 2000, 473 (01) :47-52
[3]   Bioconductor: open software development for computational biology and bioinformatics [J].
Gentleman, RC ;
Carey, VJ ;
Bates, DM ;
Bolstad, B ;
Dettling, M ;
Dudoit, S ;
Ellis, B ;
Gautier, L ;
Ge, YC ;
Gentry, J ;
Hornik, K ;
Hothorn, T ;
Huber, W ;
Iacus, S ;
Irizarry, R ;
Leisch, F ;
Li, C ;
Maechler, M ;
Rossini, AJ ;
Sawitzki, G ;
Smith, C ;
Smyth, G ;
Tierney, L ;
Yang, JYH ;
Zhang, JH .
GENOME BIOLOGY, 2004, 5 (10)
[4]  
GITLITS VM, 2001, J INVEST MED, V491, P38
[5]   Proteomics-based identification of α-enolase as a tumor antigen in non-small lung cancer [J].
He, Ping ;
Naka, Tetsuji ;
Serada, Satoshi ;
Fujimoto, Minoru ;
Tanaka, Toshio ;
Hashimoto, Shoji ;
Shima, Yoshihito ;
Yamadori, Tomoki ;
Suzuki, Hidekazu ;
Hirashima, Tomonori ;
Matsui, Kaoru ;
Shiono, Hiroyuki ;
Okumura, Meinoshin ;
Nishida, Toshiro ;
Tachibana, Isao ;
Norioka, Naoko ;
Norioka, Shigemi ;
Kawase, Ichiro .
CANCER SCIENCE, 2007, 98 (08) :1234-1240
[6]   YEAST HEAT-SHOCK PROTEIN OF MR 48,000 IS AN ISOPROTEIN OF ENOLASE [J].
IIDA, H ;
YAHARA, I .
NATURE, 1985, 315 (6021) :688-690
[7]   Exploration, normalization, and summaries of high density oligonucleotide array probe level data [J].
Irizarry, RA ;
Hobbs, B ;
Collin, F ;
Beazer-Barclay, YD ;
Antonellis, KJ ;
Scherf, U ;
Speed, TP .
BIOSTATISTICS, 2003, 4 (02) :249-264
[8]   Two enzymes in one: Two yeast peroxiredoxins display oxidative stress-dependent switching from a peroxidase to a molecular chaperone function [J].
Jang, HH ;
Lee, KO ;
Chi, YH ;
Jung, BG ;
Park, SK ;
Park, JH ;
Lee, JR ;
Lee, SS ;
Moon, JC ;
Yun, JW ;
Choi, YO ;
Kim, WY ;
Kang, JS ;
Cheong, GW ;
Yun, DJ ;
Rhee, SG ;
Cho, MJ ;
Lee, SY .
CELL, 2004, 117 (05) :625-635
[9]   Essential role for the peroxiredoxin Prdx1 in erythrocyte antioxidant defence and tumour suppression [J].
Neumann, CA ;
Krause, DS ;
Carman, CV ;
Das, S ;
Dubey, DP ;
Abraham, JL ;
Bronson, RT ;
Fujiwara, Y ;
Orkin, SH ;
Van Etten, RA .
NATURE, 2003, 424 (6948) :561-565
[10]   α-enolase, a novel strong plasmin(ogen) binding protein on the surface of pathogenic streptococci [J].
Pancholi, V ;
Fischetti, VA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (23) :14503-14515