The implications of structured 5′ untranslated regions on translation and disease

被引:264
作者
Pickering, BM
Willis, AE
机构
[1] Southampton Gen Hosp, CRC Wessex Med Oncol Unit, Southampton SO16 6YD, Hants, England
[2] Univ Leicester, Dept Biochem, Leicester LE1 7RH, Leics, England
基金
英国生物技术与生命科学研究理事会;
关键词
internal ribosome entry; 5 ' untranslated region; IRES; translation;
D O I
10.1016/j.semcdb.2004.11.006
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Translational control is a key step in eukaryotic gene expression. The majority of translational control occurs at the level of initiation, thus implicating the 5' untranslated region as a major site of translational regulation. Many growth-related mRNAs have atypical 5' UTRs, which are often long and GC-rich. Such features promote formation of stable secondary structure, and many mRNAs encoding proteins involved in cell growth, proliferation and apoptosis have structured 5' UTRs, which in many cases harbour internal ribosome entry sites (IRESs) and upstream open-reading frames (uORFs). In this review we discuss how secondary structural elements in the 5' UTR can regulate translation and how mutations that perturb these secondary structural elements can have implications for disease and tumourigenesis. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:39 / 47
页数:9
相关论文
共 86 条
  • [1] Chemistry and biology of eukaryotic iron metabolism
    Aisen, P
    Enns, C
    Wessling-Resnick, M
    [J]. INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 2001, 33 (10) : 940 - 959
  • [2] Regulation of vascular endothelial growth factor (VEGF) expression is mediated by internal initiation of translation and alternative initiation of transcription
    Akiri, G
    Nahari, D
    Finkelstein, Y
    Le, SY
    Elroy-Stein, O
    Levi, BZ
    [J]. ONCOGENE, 1998, 17 (02) : 227 - 236
  • [3] Clinical severity and thermodynamic effects of iron-responsive element mutations in hereditary hyperferritinemia-cataract syndrome
    Allerson, CR
    Cazzola, M
    Rouault, TA
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (37) : 26439 - 26447
  • [4] Translational control elements in the major human transforming growth factor-β1 mRNA
    Allison, RSH
    Mumy, ML
    Wakefield, LM
    [J]. GROWTH FACTORS, 1998, 16 (02) : 89 - 100
  • [5] INHIBITION OF TRANSLATION OF TRANSFORMING GROWTH FACTOR-BETA-3 MESSENGER-RNA BY ITS 5' UNTRANSLATED REGION
    ARRICK, BA
    LEE, AL
    GRENDELL, RL
    DERYNCK, R
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1991, 11 (09) : 4306 - 4313
  • [6] ENHANCED TRANSLATIONAL EFFICIENCY OF A NOVEL TRANSFORMING GROWTH FACTOR-BETA-3 MESSENGER-RNA IN HUMAN BREAST-CANCER CELLS
    ARRICK, BA
    GRENDELL, RL
    GRIFFIN, LA
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1994, 14 (01) : 619 - 628
  • [7] Belsham GJ, 2000, COLD SPRING HARBOR M, V39, P869
  • [8] IRESdb:: the internal ribosome entry site database
    Bonnal, S
    Boutonnet, C
    Prado-Lourenço, L
    Vagner, S
    [J]. NUCLEIC ACIDS RESEARCH, 2003, 31 (01) : 427 - 428
  • [9] Overexpression of MDM2, due to enhanced translation, results in inactivation of wild-type p53 in Burkitt's lymphoma cells
    Capoulade, C
    Bressac-de Paillerets, B
    Lefrère, I
    Ronsin, M
    Feunteun, J
    Tursz, T
    Wiels, J
    [J]. ONCOGENE, 1998, 16 (12) : 1603 - 1610
  • [10] Apoptosis of tumoral and nontumoral lymphoid cells is induced by both mdm2 and p53 antisense oligodeoxynucleotides
    Capoulade, C
    Mir, LM
    Carlier, K
    Lécluse, Y
    Tétaud, C
    Mishal, Z
    Wiels, J
    [J]. BLOOD, 2001, 97 (04) : 1043 - 1049