Mechanisms Regulating Protein Localization

被引:112
作者
Bauer, Nicholas C. [1 ,2 ]
Doetsch, Paul W. [1 ,3 ,4 ,5 ]
Corbett, Anita H. [1 ,3 ]
机构
[1] Emory Univ, Sch Med, Dept Biochem, Atlanta, GA 30322 USA
[2] Emory Univ, Sch Med, Grad Program Biochem Cell & Dev Biol, Atlanta, GA 30322 USA
[3] Emory Univ, Sch Med, Winship Canc Inst, Atlanta, GA 30322 USA
[4] Emory Univ, Sch Med, Dept Radiat Oncol, Atlanta, GA 30322 USA
[5] Emory Univ, Sch Med, Dept Hematol & Med Oncol, Atlanta, GA 30322 USA
基金
美国国家卫生研究院;
关键词
localization; nuclear import; nuclear pore; regulation; NUCLEAR-PORE COMPLEX; SIGNAL RECOGNITION PROTEIN; ELEMENT-BINDING PROTEIN; SYNTHESIZING SECRETORY PROTEIN; DAMAGE-INDUCED PHOSPHORYLATION; KINESIN-RELATED PROTEIN; HORMONE-RELATED PROTEIN; URACIL-DNA GLYCOSYLASE; ENDOPLASMIC-RETICULUM; SACCHAROMYCES-CEREVISIAE;
D O I
10.1111/tra.12310
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Cellular functions are dictated by protein content and activity. There are numerous strategies to regulate proteins varying from modulating gene expression to post-translational modifications. One commonly used mode of regulation in eukaryotes is targeted localization. By specifically redirecting the localization of a pool of existing protein, cells can achieve rapid changes in local protein function. Eukaryotic cells have evolved elegant targeting pathways to direct proteins to the appropriate cellular location or locations. Here, we provide a general overview of these localization pathways, with a focus on nuclear and mitochondrial transport, and present a survey of the evolutionarily conserved regulatory strategies identified thus far. We end with a description of several specific examples of proteins that exploit localization as an important mode of regulation.
引用
收藏
页码:1039 / 1061
页数:23
相关论文
共 225 条
[1]   Structural basis of presequence recognition by the mitochondrial protein import receptor Tom20 [J].
Abe, Y ;
Shodai, T ;
Muto, T ;
Mihara, K ;
Torii, H ;
Nishikawa, S ;
Endo, T ;
Kohda, D .
CELL, 2000, 100 (05) :551-560
[2]   Different organization of base excision repair of uracil in DNA in nuclei and mitochondria and selective upregulation of mitochondrial uracil-DNA glycosylase after oxidative stress [J].
Akbari, M. ;
Otterlei, M. ;
Pena-Diaz, J. ;
Krokan, H. E. .
NEUROSCIENCE, 2007, 145 (04) :1201-1212
[3]   NUCLEAR TRANSLOCATION OF BASIC FIBROBLAST GROWTH-FACTOR [J].
AMALRIC, F ;
BALDIN, V ;
BOSCBIERNE, I ;
BUGLER, B ;
COUDERC, B ;
GUYADER, M ;
PATRY, V ;
PRATS, H ;
ROMAN, AM ;
BOUCHE, G .
ANNALS OF THE NEW YORK ACADEMY OF SCIENCES, 1991, 638 :127-138
[4]   The Tangled Circuitry of Metabolism and Apoptosis [J].
Andersen, Joshua L. ;
Kornbluth, Sally .
MOLECULAR CELL, 2013, 49 (03) :399-410
[5]   Structural Basis for Ligand Regulation of the Fatty Acid-binding Protein 5, Peroxisome Proliferator-activated Receptor β/δ (FABP5-PPAR β/δ) Signaling Pathway [J].
Armstrong, Eric H. ;
Goswami, Devrishi ;
Griffin, Patrick R. ;
Noy, Noa ;
Ortlund, Eric A. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2014, 289 (21) :14941-14954
[6]   Myristoylation of p39 and p35 is a determinant of cytoplasmic or nuclear localization of active cycline-dependent kinase 5 complexes [J].
Asada, Akiko ;
Yamamoto, Naoyuki ;
Gohda, Masaki ;
Saito, Taro ;
Hayashi, Nobuhiro ;
Hisanaga, Shin-ichi .
JOURNAL OF NEUROCHEMISTRY, 2008, 106 (03) :1325-1336
[7]   Phosphorylation of p35 and p39 by Cdk5 determines the subcellular location of the holokinase in a phosphorylation-site-specific manner [J].
Asada, Akiko ;
Saito, Taro ;
Hisanaga, Shin-ichi .
JOURNAL OF CELL SCIENCE, 2012, 125 (14) :3421-3429
[8]   Embracing the void-how much do we really know about targeting and translocation to the endoplasmic reticulum? [J].
Aviram, Naama ;
Schuldiner, Maya .
CURRENT OPINION IN CELL BIOLOGY, 2014, 29 :8-17
[9]   Proteolysis that is inhibited by Hedgehog targets Cubitus interruptus protein to the nucleus and converts it to a repressor [J].
AzaBlanc, P ;
RamirezWeber, FA ;
Laget, MP ;
Schwartz, C ;
Kornberg, TB .
CELL, 1997, 89 (07) :1043-1053
[10]   TRANSLOCATION OF BFGF TO THE NUCLEUS IS G1 PHASE CELL-CYCLE SPECIFIC IN BOVINE AORTIC ENDOTHELIAL-CELLS [J].
BALDIN, V ;
ROMAN, AM ;
BOSCBIERNE, I ;
AMALRIC, F ;
BOUCHE, G .
EMBO JOURNAL, 1990, 9 (05) :1511-1517