The unfolded protein response: No longer just a special teams player

被引:44
作者
Spear, E [1 ]
Ng, DTW [1 ]
机构
[1] Penn State Univ, Dept Biochem & Mol Biol, University Pk, PA 16802 USA
关键词
endoplasmic reticulum; ER-associated protein degradation; gene regulation; secretory pathway; signal transduction; unfolded protein response;
D O I
10.1034/j.1600-0854.2001.20801.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The endoplasmic reticulum stress pathway known as the unfolded protein response is currently the best understood model of interorganellar signal transduction. Bridging a physical separation, the pathway provides a direct line of communication between the endoplasmic reticulum lumen and the nucleus. With the unfolded protein response, the cell has the means to monitor and respond to the changing needs of the endoplasmic reticulum. Beginning with the discovery of its remarkable signaling mechanism in yeast, the unfolded protein response has not ceased to reveal more of its many secrets. By applying powerful biochemical, genetic, genomic, and cytological approaches, the recent efforts of many groups have buried the long-held notion that the unfolded protein response is simply a regulatory platform for endoplasmic reticulum chaperones. We now know that the unfolded protein response regulates many genes that affect diverse aspects of cellular physiology. In addition, studies in mammals have revealed novel unfolded protein response signaling factors that may contribute to the specialized needs of multicellular organisms. This article focuses on these and other recent developments in the field.
引用
收藏
页码:515 / 523
页数:9
相关论文
共 65 条
[1]   Dynamic interaction of BiP and ER stress transducers in the unfolded-protein response [J].
Bertolotti, A ;
Zhang, YH ;
Hendershot, LM ;
Harding, HP ;
Ron, D .
NATURE CELL BIOLOGY, 2000, 2 (06) :326-332
[2]   Increased sensitivity to dextran sodium sulfate colitis in IRE1β-deficient mice [J].
Bertolotti, A ;
Wang, XZ ;
Novoa, I ;
Jungreis, R ;
Schlessinger, K ;
Cho, JH ;
West, AB ;
Ron, D .
JOURNAL OF CLINICAL INVESTIGATION, 2001, 107 (05) :585-593
[3]   A pathway distinct from the mammalian unfolded protein response regulates expression of endoplasmic reticulum chaperones in non-stressed cells [J].
Brewer, JW ;
Cleveland, JL ;
Hendershot, LM .
EMBO JOURNAL, 1997, 16 (23) :7207-7216
[4]   The requirement for molecular chaperones during endoplasmic reticulum-associated protein degradation demonstrates that protein export and import are mechanistically distinct [J].
Brodsky, JL ;
Werner, ED ;
Dubas, ME ;
Goeckeler, JL ;
Kruse, KB ;
McCracken, AA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (06) :3453-3460
[5]  
BRODSKY JL, 1999, IN PRESS CELL DEV BI
[6]  
BROSTROM CO, 1989, J BIOL CHEM, V264, P1644
[7]   Regulated intramembrane proteolysis: A control mechanism conserved from bacteria to humans [J].
Brown, MS ;
Ye, J ;
Rawson, RB ;
Goldstein, JL .
CELL, 2000, 100 (04) :391-398
[8]   Conformational changes and disease - serpins, prions and Alzheimer's [J].
Carrell, RW ;
Gooptu, B .
CURRENT OPINION IN STRUCTURAL BIOLOGY, 1998, 8 (06) :799-809
[9]   Degradation of proteins from the ER of S-cerevisiae requires an intact unfolded protein response pathway [J].
Casagrande, R ;
Stern, P ;
Diehn, M ;
Shamu, C ;
Osario, M ;
Zúñiga, M ;
Brown, PO ;
Ploegh, H .
MOLECULAR CELL, 2000, 5 (04) :729-735
[10]   Translational attenuation mediated by an mRNA intron [J].
Chapman, RE ;
Walter, P .
CURRENT BIOLOGY, 1997, 7 (11) :850-859