Degradation of the Endoplasmic Reticulum by Autophagy during Endoplasmic Reticulum Stress in Arabidopsis

被引:217
|
作者
Liu, Yimo [1 ,2 ]
Burgos, Junmarie Soto [1 ]
Deng, Yan [3 ]
Srivastava, Renu [3 ]
Howell, Stephen H. [1 ,3 ]
Bassham, Diane C. [1 ,2 ,3 ]
机构
[1] Iowa State Univ, Dept Genet Dev & Cell Biol, Ames, IA 50011 USA
[2] Iowa State Univ, Interdept Genet Program, Ames, IA 50011 USA
[3] Iowa State Univ, Inst Plant Sci, Ames, IA 50011 USA
来源
PLANT CELL | 2012年 / 24卷 / 11期
基金
美国国家科学基金会;
关键词
UNFOLDED PROTEIN-RESPONSE; ACTIVE TRANSCRIPTION FACTOR; KAR2 BIP GENE; TRANSMEMBRANE PROTEIN; SELECTIVE AUTOPHAGY; MESSENGER-RNA; ER STRESS; GOLGI-APPARATUS; PLANT AUTOPHAGY; CELL-SURVIVAL;
D O I
10.1105/tpc.112.101535
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
In this article, we show that the endoplasmic reticulum (ER) in Arabidopsis thaliana undergoes morphological changes in structure during ER stress that can be attributed to autophagy. ER stress agents trigger autophagy as demonstrated by increased production of autophagosomes. In response to ER stress, a soluble ER marker localizes to autophagosomes and accumulates in the vacuole upon inhibition of vacuolar proteases. Membrane lamellae decorated with ribosomes were observed inside autophagic bodies, demonstrating that portions of the ER are delivered to the vacuole by autophagy during ER stress. In addition, an ER stress sensor, INOSITOL-REQUIRING ENZYME-1b (IRE1b), was found to be required for ER stress-induced autophagy. However, the IRE1b splicing target, bZIP60, did not seem to be involved, suggesting the existence of an undiscovered signaling pathway to regulate ER stress-induced autophagy in plants. Together, these results suggest that autophagy serves as a pathway for the turnover of ER membrane and its contents in response to ER stress in plants.
引用
收藏
页码:4635 / 4651
页数:17
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