Post-transcriptional regulation of gene expression by degradation of messenger RNAs

被引:260
作者
Bevilacqua, A
Ceriani, MC
Capaccioli, S
Nicolin, A
机构
[1] Univ Milan, Dept Pharmacol, I-20129 Milan, Italy
[2] Univ Florence, Dept Expt Pathol & Oncol, Florence, Italy
关键词
D O I
10.1002/jcp.10272
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Recent evidence suggests that gene expression may be regulated, at least in part, at post-transcriptional level by factors inducing the extremely rapid degradation of messenger RNAs. These factors include reactions between adenyl-uridyl-rich elements (AREs) of the relevant mRNA and either specific proteins that bind to these elements or exosomes. This review deals with examples of the proteins (AU-rich binding proteins, AUBPs) and exosomes, which have been shown to form complexes with AREs and bring about rapid degradation of the relevant mRNA, and with certain other factors, which protect the RNA from such degradation. The biochemical and physiological factors underlying the stability of messenger RNAs carrying the ARE motifs will be reviewed in the light of their emerging significance for cell physiology, human pathology, and molecular medicine. We also consider the possible application of the results of recent insights into the mechanisms to pharmacological interventions to prevent or cure disorders, especially develop. mental disorders, which the suppression of gene expression may bring about. Molecular targeting of specific steps in protein degradation by synthetic compounds has already been utilized for the development of pharmacological therapies. (C) 2003 Wiley-Liss, Inc.
引用
收藏
页码:356 / 372
页数:17
相关论文
共 200 条
[1]   SELECTIVE DESTABILIZATION OF SHORT-LIVED MESSENGER-RNAS WITH THE GRANULOCYTE-MACROPHAGE COLONY-STIMULATING FACTOR AU-RICH 3' NONCODING REGION IS MEDIATED BY A COTRANSLATIONAL MECHANISM [J].
AHARON, T ;
SCHNEIDER, RJ .
MOLECULAR AND CELLULAR BIOLOGY, 1993, 13 (03) :1971-1980
[2]  
AKASHI M, 1994, BLOOD, V83, P3182
[3]   The yeast exosome and human PM-Scl are related complexes of 3′→5′ exonucleases [J].
Allmang, C ;
Petfalski, E ;
Podtelejnikov, A ;
Mann, M ;
Tollervey, D ;
Mitchell, P .
GENES & DEVELOPMENT, 1999, 13 (16) :2148-2158
[4]   The 3′ to 5′ degradation of yeast mRNAs is a general mechanism for mRNA turnover that requires the SKI2 DEVH box protein and 3′ to 5′ exonucleases of the exosome complex [J].
Anderson, JSJ ;
Parker, R .
EMBO JOURNAL, 1998, 17 (05) :1497-1506
[5]   Embryonic lethal abnormal visual RNA-binding proteins involved in growth, differentiation, and posttranscriptional gene expression [J].
Antic, D ;
Keene, JD .
AMERICAN JOURNAL OF HUMAN GENETICS, 1997, 61 (02) :273-278
[6]  
Antic D, 1998, J CELL SCI, V111, P183
[7]   Ski7p G protein interacts with the exosome and the Ski complex for 3′-to-5′ mRNA decay in yeast [J].
Araki, Y ;
Takahashi, S ;
Kobayashi, T ;
Kajiho, H ;
Hoshino, S ;
Katada, T .
EMBO JOURNAL, 2001, 20 (17) :4684-4693
[8]   A nuclear matrix-associated factor, SAF-B, interacts with specific isoforms of AUF1/hnRNP D [J].
Arao, Y ;
Kuriyama, R ;
Kayama, F ;
Kato, S .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 2000, 380 (02) :228-236
[9]   EVOLUTIONARY CONSERVATION OF THE AU-RICH 3' UNTRANSLATED REGION OF MESSENGER-RNA [J].
ASSONBATRES, MA ;
SPURGEON, SL ;
DIAZ, J ;
DELOUGHERY, TG ;
BAGBY, GC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (04) :1318-1322
[10]   AN AMINO-TERMINAL TETRAPEPTIDE SPECIFIES COTRANSLATIONAL DEGRADATION OF BETA-TUBULIN BUT NOT ALPHA-TUBULIN MESSENGER-RNAS [J].
BACHURSKI, CJ ;
THEODORAKIS, NG ;
COULSON, RMR ;
CLEVELAND, DW .
MOLECULAR AND CELLULAR BIOLOGY, 1994, 14 (06) :4076-4086