TOP mRNPs: Molecular Mechanisms and Principles of Regulation

被引:45
作者
Cockman, Eric [1 ]
Anderson, Paul [2 ]
Ivanov, Pavel [2 ]
机构
[1] Harvard Med Sch, Brigham & Womens Hosp, Boston, MA 02115 USA
[2] Harvard Med Sch, Brigham & Womens Hosp, Harvard Initiat RNA Med, Boston, MA 02115 USA
基金
美国国家卫生研究院;
关键词
5 ' Terminal Oligopyrimidine; RNA binding proteins; LARP1; translation regulation; RNA; MESSENGER-RNA TRANSLATION; BINDING PROTEIN LARP1; AU-RICH ELEMENT; LA PROTEIN; STRESS GRANULES; STRUCTURAL-ANALYSIS; RECOGNITION; MOTIF; PHOSPHORYLATION; TIA-1;
D O I
10.3390/biom10070969
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
The cellular response to changes in the surrounding environment and to stress requires the coregulation of gene networks aiming to conserve energy and resources. This is often achieved by downregulating protein synthesis. The 5' Terminal OligoPyrimidine (5' TOP) motif-containing mRNAs, which encode proteins that are essential for protein synthesis, are the primary targets of translational control under stress. The TOP motif is a cis-regulatory RNA element that begins directly after the m7G cap structure and contains the hallmark invariant 5'-cytidine followed by an uninterrupted tract of 4-15 pyrimidines. Regulation of translation via the TOP motif coordinates global protein synthesis with simultaneous co-expression of the protein components required for ribosome biogenesis. In this review, we discuss architecture of TOP mRNA-containing ribonucleoprotein complexes, the principles of their assembly, and the modes of regulation of TOP mRNA translation.
引用
收藏
页码:1 / 18
页数:18
相关论文
共 96 条
  • [11] The RNA binding protein Larp1 regulates cell division, apoptosis and cell migration
    Burrows, Carla
    Latip, Normala Abd
    Lam, Sarah-Jane
    Carpenter, Lee
    Sawicka, Kirsty
    Tzolovsky, George
    Gabra, Hani
    Bushell, Martin
    Glover, David M.
    Willis, Anne E.
    Blagden, Sarah P.
    [J]. NUCLEIC ACIDS RESEARCH, 2010, 38 (16) : 5542 - 5553
  • [12] Synthesis and function of ribosomal proteins - fading models and new perspectives
    Caldarola, Sara
    De Stefano, Maria Chiara
    Amaldi, Francesco
    Loreni, Fabrizio
    [J]. FEBS JOURNAL, 2009, 276 (12) : 3199 - 3210
  • [13] La protein is associated with terminal oligopyrimidine mRNAs in actively translating polysomes
    Cardinali, B
    Carissimi, C
    Gravina, P
    Pierandrei-Amaldi, P
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (37) : 35145 - 35151
  • [14] The La protein functions redundantly with tRNA modification enzymes to ensure tRNA structural stability
    Copela, LA
    Chakshusmathi, G
    Sherrer, RL
    Wolin, SL
    [J]. RNA, 2006, 12 (04) : 644 - 654
  • [15] La protein has a positive effect on the translation of TOP mRNAs in vivo
    Crosio, C
    Boyl, PP
    Loreni, F
    Pierandrei-Amaldi, P
    Amaldi, F
    [J]. NUCLEIC ACIDS RESEARCH, 2000, 28 (15) : 2927 - 2934
  • [16] Translational coregulation of 5′TOP mRNAs by TIA-1 and TIAR
    Damgaard, Christian Kroun
    Lykke-Andersen, Jens
    [J]. GENES & DEVELOPMENT, 2011, 25 (19) : 2057 - 2068
  • [17] Identification and functional outcome of mRNAs associated with RNA-binding protein TIA-1
    de Silanes, IL
    Galbán, S
    Martindale, JL
    Yang, XL
    Mazan-Mamczarz, K
    Indig, FE
    Falco, G
    Zhan, M
    Gorospe, M
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 2005, 25 (21) : 9520 - 9531
  • [18] Structural determinants in AUF1 required for high affinity binding to A+U-rich elements
    DeMaria, CT
    Sun, Y
    Long, L
    Wagner, BJ
    Brewer, G
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (44) : 27635 - 27643
  • [19] Individual RNA recognition motifs of TIA-1 and TIAR have different RNA binding specificities
    Dember, LM
    Kim, ND
    Liu, KQ
    Anderson, P
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (05) : 2783 - 2788
  • [20] RNA G-Quadruplexes in Biology: Principles and Molecular Mechanisms
    Fay, Marta M.
    Lyons, Shawn M.
    Ivanov, Pavel
    [J]. JOURNAL OF MOLECULAR BIOLOGY, 2017, 429 (14) : 2127 - 2147