Post-transcriptional regulation of gene expression by mitogen-activated protein kinase p38

被引:197
作者
Clark, AR [1 ]
Dean, JLE [1 ]
Saklatvala, J [1 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Fac Med, Kennedy Inst, Div Rheumatol, London W6 8LH, England
关键词
adenosine/uridine rich element; MAPK p38; MAPKAPK-2; mRNA stability; translation; inflammation;
D O I
10.1016/S0014-5793(03)00439-3
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
The mitogen-activated protein kinase p38 pathway was originally identified as a signalling cascade activated by pro-inflammatory stimuli and cellular stresses, and playing a critical role in the translational regulation of pro-inflammatory cytokine synthesis. In almost a decade since this discovery, a great deal has been learned about the role of the p38 pathway in the post-transcriptional regulation of pro-inflammatory gene expression. However, important questions remain to be answered concerning the specificity and mechanism or mechanisms of action of p38. This review describes recent progress and remaining puzzles in the field of post-transcriptional regulation by p38. (C) 2003 Published by Elsevier Science B.V. on behalf of the Federation of European Biochemical Societies.
引用
收藏
页码:37 / 44
页数:8
相关论文
共 111 条
[1]
Two different RNA binding activities for the AU-rich element and the poly(A) sequence of the mouse neuronal protein mHuC [J].
Abe, R ;
Sakashita, E ;
Yamamoto, K ;
Sakamoto, H .
NUCLEIC ACIDS RESEARCH, 1996, 24 (24) :4895-4901
[2]
AMANO Y, 1993, MOL PHARMACOL, V43, P176
[3]
Negative feedback regulation of MKK6 mRNA stability by p38α mitogen-activated protein kinase [J].
Ambrosino, C ;
Mace, G ;
Galban, S ;
Fritsch, C ;
Vintersten, K ;
Black, E ;
Gorospe, M ;
Nebreda, AR .
MOLECULAR AND CELLULAR BIOLOGY, 2003, 23 (01) :370-381
[4]
The role of p38 in UVA-induced cyclooxygenase-2 expression in the human keratinocyte cell line, HaCaT [J].
Bachelor, MA ;
Silvers, AL ;
Bowden, GT .
ONCOGENE, 2002, 21 (46) :7092-7099
[5]
BERKMAN N, 1995, J IMMUNOL, V155, P4412
[6]
CORTICOSTEROID INHIBITION OF MACROPHAGE INFLAMMATORY PROTEIN-1-ALPHA IN HUMAN MONOCYTES AND ALVEOLAR MACROPHAGES [J].
BERKMAN, N ;
JOSE, PJ ;
WILLIAMS, TJ ;
SCHALL, TJ ;
BARNES, PJ ;
CHUNG, KF .
AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 1995, 269 (04) :L443-L452
[7]
BOGDAN C, 1992, J BIOL CHEM, V267, P23301
[8]
Affinity purification of ARE-binding proteins identifies poly(A)-binding protein 1 as a potential substrate in MK2-induced mRNA stabilization [J].
Bollig, F ;
Winzen, R ;
Gaestel, M ;
Kostka, S ;
Resch, K ;
Holtmann, H .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2003, 301 (03) :665-670
[9]
HuR and mRNA stability [J].
Brennan, CM ;
Steitz, JA .
CELLULAR AND MOLECULAR LIFE SCIENCES, 2001, 58 (02) :266-277
[10]
POLY(A) SHORTENING AND DEGRADATION OF THE 3' A+U-RICH SEQUENCES OF HUMAN C-MYC MESSENGER-RNA IN A CELL-FREE SYSTEM [J].
BREWER, G ;
ROSS, J .
MOLECULAR AND CELLULAR BIOLOGY, 1988, 8 (04) :1697-1708