Micro(RNA)managing Endoplasmic Reticulum Stress

被引:48
作者
Byrd, Andrew E. [1 ]
Brewer, Joseph W. [1 ]
机构
[1] Univ S Alabama, Dept Microbiol & Immunol, Coll Med, Mobile, AL 36688 USA
基金
美国国家卫生研究院;
关键词
microRNA; endoplasmic reticulum stress; unfolded protein response; adaptation; apoptosis; UNFOLDED PROTEIN RESPONSE; THIOREDOXIN-INTERACTING PROTEIN; QUALITY-CONTROL PROTEINS; PROGRAMMED CELL-DEATH; ER STRESS; MESSENGER-RNA; MIR-23A-SIMILAR-TO-27A-SIMILAR-TO-24-2; CLUSTER; POSTTRANSCRIPTIONAL REGULATION; INDUCED APOPTOSIS; GENE-EXPRESSION;
D O I
10.1002/iub.1151
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
Cellular disturbances that cause accumulation of misfolded proteins in the endoplasmic reticulum (ER) lead to a condition referred to as ER stress and trigger the unfolded protein response (UPR), a signaling pathway that attempts to restore ER homeostasis. The complexity of UPR signaling can generate adaptive and apoptotic outputs, depending on the nature and duration of the ER stress. MicroRNAs (miRNAs), small non-coding RNAs that typically repress gene expression, have recently emerged as key gene regulators of the proadaptive/proapoptotic molecular switch emanating from the ER. Importantly, select miRNAs have been shown to directly regulate key UPR components. (c) 2013 IUBMB Life, 65(5):373381, 2013.
引用
收藏
页码:373 / 381
页数:9
相关论文
共 80 条
  • [1] ATF6 Is a Transcription Factor Specializing in the Regulation of Quality Control Proteins in the Endoplasmic Reticulum
    Adachi, Yusuke
    Yamamoto, Keisuke
    Okada, Tetsuya
    Yoshida, Hiderou
    Harada, Akihiro
    Mori, Kazutoshi
    [J]. CELL STRUCTURE AND FUNCTION, 2008, 33 (01) : 75 - 89
  • [2] Permissive role of miR-663 in induction of VEGF and activation of the ATF4 branch of unfolded protein response in endothelial cells by oxidized phospholipids
    Afonyushkin, Taras
    Oskolkova, Olga V.
    Bochkov, Valery N.
    [J]. ATHEROSCLEROSIS, 2012, 225 (01) : 50 - 55
  • [3] A uniform system for microRNA annotation
    Ambros, V
    Bartel, B
    Bartel, DP
    Burge, CB
    Carrington, JC
    Chen, XM
    Dreyfuss, G
    Eddy, SR
    Griffiths-Jones, S
    Marshall, M
    Matzke, M
    Ruvkun, G
    Tuschl, T
    [J]. RNA, 2003, 9 (03) : 277 - 279
  • [4] MicroRNAs: Target Recognition and Regulatory Functions
    Bartel, David P.
    [J]. CELL, 2009, 136 (02) : 215 - 233
  • [5] The Unfolded Protein Response (UPR)-activated Transcription Factor X-box-binding Protein 1 (XBP1) Induces MicroRNA-346 Expression That Targets the Human Antigen Peptide Transporter 1 (TAP1) mRNA and Governs Immune Regulatory Genes
    Bartoszewski, Rafal
    Brewer, Joseph W.
    Rab, Andras
    Crossman, David K.
    Bartoszewska, Sylwia
    Kapoor, Niren
    Fuller, Cathy
    Collawn, James F.
    Bebok, Zsuzsa
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2011, 286 (48) : 41862 - 41870
  • [6] A CHOP-regulated microRNA controls rhodopsin expression
    Behrman, Shannon
    Acosta-Alvear, Diego
    Walter, Peter
    [J]. JOURNAL OF CELL BIOLOGY, 2011, 192 (06) : 919 - 927
  • [7] Regulation of microRNA expression in the heart by the ATF6 branch of the ER stress response
    Belmont, Peter J.
    Chen, Wenqiong J.
    Thuerauf, Donna J.
    Glembotski, Christopher C.
    [J]. JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 2012, 52 (05) : 1176 - 1182
  • [8] Principles of MicroRNA-target recognition
    Brennecke, J
    Stark, A
    Russell, RB
    Cohen, SM
    [J]. PLOS BIOLOGY, 2005, 3 (03): : 404 - 418
  • [9] MicroRNA-30c-2*limits expression of proadaptive factor XBP1 in the unfolded protein response
    Byrd, Andrew E.
    Aragon, Ileana V.
    Brewer, Joseph W.
    [J]. JOURNAL OF CELL BIOLOGY, 2012, 196 (06) : 689 - 698
  • [10] IRE1 couples endoplasmic reticulum load to secretory capacity by processing the XBP-1 mRNA
    Calfon, M
    Zeng, HQ
    Urano, F
    Till, JH
    Hubbard, SR
    Harding, HP
    Clark, SG
    Ron, D
    [J]. NATURE, 2002, 415 (6867) : 92 - 96