Bax induces activation of the unfolded protein response by inducing HAC1 mRNA splicing in Saccharomyces cerevisiae

被引:9
作者
Cakir, Birsen [1 ,2 ,3 ]
机构
[1] Ege Univ, Fac Agr, Dept Hort, Izmir, Turkey
[2] Rutgers State Univ, Biotechnol Ctr Agr & Environm, New Brunswick, NJ 08903 USA
[3] Rutgers State Univ, Cook Coll, Dept Plant Biol & Pathol, New Brunswick, NJ 08903 USA
关键词
cell death; Bax; unfolded protein response; yeast; apoptosis; CYTOCHROME-C RELEASE; INDUCED CASPASE ACTIVATION; STRESS-INDUCED APOPTOSIS; ENDOPLASMIC-RETICULUM; CELL-DEATH; PROAPOPTOTIC BAX; GENE-EXPRESSION; BCL-2; ER; MITOCHONDRIA;
D O I
10.1002/yea.2918
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
Bax, a multidomain pro-apoptotic Bcl-2 protein, localizes to the endoplasmic reticulum (ER), where it regulates ER stress-induced apoptosis. Adaptation to ER stress depends on the activation of an integrated signal transduction pathway known as the unfolded protein response (UPR). This study examined the death-inducing activity of Bax and its ability to induce UPR signalling pathways in yeast. We observed that inhibition of global translation in yeast cells expressing Bax correlated with Bax-induced cell death. Using a lacZ reporter containing several UPR cis-activating regulatory elements, we also found that Bax directly activated the UPR. Furthermore, this correlated with the splicing of HAC1 mRNA, a gene involved in UPR activation. Bax induced expression of representative UPR target genes such as KAR2, DER1 and GCN4. Finally, we found that Ire1p function is critical for Bax-induced cell death. Copyright (C) 2012 John Wiley & Sons, Ltd.
引用
收藏
页码:395 / 406
页数:12
相关论文
共 67 条
[11]   Bcl-2 functionally interacts with inositol 1,4,5-trisphosphate receptors to regulate calcium release from the ER in response to inositol 1,4,5-trisphosphate [J].
Chen, R ;
Valencia, I ;
Zhong, F ;
McColl, KS ;
Roderick, HL ;
Bootman, MD ;
Berridge, MJ ;
Conway, SJ ;
Holmes, AB ;
Mignery, GA ;
Velez, P ;
Distelhorst, CW .
JOURNAL OF CELL BIOLOGY, 2004, 166 (02) :193-203
[12]   TRANSCRIPTIONAL INDUCTION OF GENES ENCODING ENDOPLASMIC-RETICULUM RESIDENT PROTEINS REQUIRES A TRANSMEMBRANE PROTEIN-KINASE [J].
COX, JS ;
SHAMU, CE ;
WALTER, P .
CELL, 1993, 73 (06) :1197-1206
[13]   A novel mechanism for regulating activity of a transcription factor that controls the unfolded protein response [J].
Cox, JS ;
Walter, P .
CELL, 1996, 87 (03) :391-404
[14]   Organelle-specific initiation of cell death pathways [J].
Ferri, KF ;
Kroemer, G .
NATURE CELL BIOLOGY, 2001, 3 (11) :E255-E263
[15]   Bax-induced caspase activation and apoptosis via cytochrome c release from mitochondria is inhibitable by Bcl-xL [J].
Finucane, DM ;
Bossy-Wetzel, E ;
Waterhouse, NJ ;
Cotter, TG ;
Green, DR .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (04) :2225-2233
[16]   BH-3-only BIK functions at the endoplasmic reticulum to stimulate cytochrome c release from mitochondria [J].
Germain, M ;
Mathai, JP ;
Shore, GC .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (20) :18053-18060
[17]   Mitochondria and apoptosis [J].
Green, DR ;
Reed, JC .
SCIENCE, 1998, 281 (5381) :1309-1312
[18]   BCL-2 family members and the mitochondria in apoptosis [J].
Gross, A ;
McDonnell, JM ;
Korsmeyer, SJ .
GENES & DEVELOPMENT, 1999, 13 (15) :1899-1911
[19]   Protein-tyrosine phosphatase 1B potentiates IRE1 signaling during endoplasmic reticulum stress [J].
Gu, F ;
Nguyên, DT ;
Stuible, M ;
Dubé, N ;
Tremblay, ML ;
Chevet, E .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (48) :49689-49693
[20]   HSP72 Protects Cells from ER Stress-induced Apoptosis via Enhancement of IRE1α-XBP1 Signaling through a Physical Interaction [J].
Gupta, Sanjeev ;
Deepti, Ayswaria ;
Deegan, Shane ;
Lisbona, Fernanda ;
Hetz, Claudio ;
Samali, Afshin .
PLOS BIOLOGY, 2010, 8 (07)