Arabidopsis IRE1 catalyses unconventional splicing of bZIP60 mRNA to produce the active transcription factor

被引:269
|
作者
Nagashima, Yukihiro [1 ]
Mishiba, Kei-ichiro [1 ]
Suzuki, Eiji [1 ]
Shimada, Yukihisa [2 ]
Iwata, Yuji [3 ,4 ,5 ]
Koizumi, Nozomu [1 ]
机构
[1] Osaka Prefecture Univ, Grad Sch Life & Environm Sci, Naka Ku, Osaka 5998531, Japan
[2] Yokohama City Univ, Kihara Inst Biol Res, Totsuka Ku, Kanagawa 2440813, Japan
[3] Penn State Univ, Dept Biol, University Pk, PA 16802 USA
[4] Penn State Univ, Huck Inst Life Sci, University Pk, PA 16802 USA
[5] King Abdullah Univ Sci & Technol, Div Chem & Life Sci & Engn, Thuwal 239556900, Saudi Arabia
来源
SCIENTIFIC REPORTS | 2011年 / 1卷
关键词
UNFOLDED PROTEIN-RESPONSE; RETICULUM STRESS-RESPONSE; ENDOPLASMIC-RETICULUM; ER-STRESS; TRANSMEMBRANE PROTEIN; FACTOR ATBZIP60; ATF6; PROTEOLYSIS; TUNICAMYCIN; THALIANA;
D O I
10.1038/srep00029
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
IRE1 plays an essential role in the endoplasmic reticulum (ER) stress response in yeast and mammals. We found that a double mutant of Arabidopsis IRE1A and IRE1B (ire1a/ire1b) is more sensitive to the ER stress inducer tunicamycin than the wild-type. Transcriptome analysis revealed that genes whose induction was reduced in ire1a/ire1b largely overlapped those in the bzip60 mutant. We observed that the active form of bZIP60 protein detected in the wild-type was missing in ire1a/ire1b. We further demonstrated that bZIP60 mRNA is spliced by ER stress, removing 23 ribonucleotides and therefore causing a frameshift that replaces the C-terminal region of bZIP60 including the transmembrane domain (TMD) with a shorter region without a TMD. This splicing was detected in ire1a and ire1b single mutants, but not in the ire1a/ire1b double mutant. We conclude that IRE1A and IRE1B catalyse unconventional splicing of bZIP60 mRNA to produce the active transcription factor.
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页数:10
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