RNA Binding Protein Regulation and Cross-Talk in the Control of AU-rich mRNA Fate

mRNA metabolism is tightly orchestrated by highly-regulated RNA Binding Proteins (RBPs) that determine mRNA fate, thereby influencing multiple cellular functions across biological contexts. Here, we review the interplay between six well-known RBPs (TTP, AUF-1, KSRP, HuR, TIA-1, and TIAR) that recognize AU-rich elements (AREs) at the 3′ untranslated regions of mRNAs, namely ARE-RBPs. Examples of the links between their cross-regulations and modulation of their targets are analyzed during mRNA processing, turnover, localization, and translational control. Furthermore, ARE recognition can be self-regulated by several factors that lead to the prevalence of one RBP over another. Consequently, we examine the factors that modulate the dynamics of those protein-RNA transient interactions to better understand the final consequences of the regulation mediated by ARE-RBPs. For instance, factors controlling the RBP isoforms, their conformational state or their post-translational modifications (PTMs) can strongly determine the fate of the protein-RNA complexes. Moreover, mRNA specific sequence and secondary structure or subtle environmental changes are also key determinants to take into account. To sum up, the whole understanding of such a fine tuned regulation is a challenge for future research and requires the integration of all the available structural and functional data by in vivo, in vitro and in silico approaches.

[1]  P. Anderson,et al.  Stress granule assembly is mediated by prion-like aggregation of TIA-1. , 2004, Molecular biology of the cell.

[2]  M. Gorospe,et al.  Reduced nuclear export of HuR mRNA by HuR is linked to the loss of HuR in replicative senescence , 2009, Nucleic acids research.

[3]  C. Zeng,et al.  Translational Repression of Human Matrix Metalloproteinases-13 by an Alternatively Spliced Form of T-cell-restricted Intracellular Antigen-related Protein (TIAR)* , 2003, The Journal of Biological Chemistry.

[4]  J. Valcárcel,et al.  Structure, dynamics and RNA binding of the multi-domain splicing factor TIA-1 , 2014, Nucleic acids research.

[5]  P. Blackshear,et al.  Necrosis Factor Alpha Mrna Deadenylation and Destabilization of Tumor Au-rich Elements and Promotes the Evidence That Tristetraprolin Binds To , 1999 .

[6]  Nooruddin Khan,et al.  Post-transcriptional Regulation of Immunological Responses through Riboclustering , 2016, Front. Immunol..

[7]  D. Dixon,et al.  The roles of TTP and BRF proteins in regulated mRNA decay , 2011, Wiley interdisciplinary reviews. RNA.

[8]  P. Blackshear,et al.  Decreased Sensitivity of Tristetraprolin-deficient Cells to p38 Inhibitors Suggests the Involvement of Tristetraprolin in the p38 Signaling Pathway* , 2001, The Journal of Biological Chemistry.

[9]  M. Mann,et al.  AU Binding Proteins Recruit the Exosome to Degrade ARE-Containing mRNAs , 2001, Cell.

[10]  Andres Ramos,et al.  The sequence selectivity of KSRP explains its flexibility in the recognition of the RNA targets , 2008, Nucleic acids research.

[11]  O. Boutaud,et al.  Tristetraprolin Binds to the 3′-Untranslated Region of Cyclooxygenase-2 mRNA , 2003, The Journal of Biological Chemistry.

[12]  F. Gebauer,et al.  Translational control by 3′-UTR-binding proteins , 2012, Briefings in functional genomics.

[13]  Mihoko Kai Roles of RNA-Binding Proteins in DNA Damage Response , 2016, International journal of molecular sciences.

[14]  G. M. Wilson,et al.  A Hairpin-like Structure within an AU-rich mRNA-destabilizing Element Regulates trans-Factor Binding Selectivity and mRNA Decay Kinetics* , 2005, Journal of Biological Chemistry.

[15]  C. Y. Chen,et al.  Unraveling a cytoplasmic role for hnRNP D in the in vivo mRNA destabilization directed by the AU-rich element. , 1999, Genes & development.

[16]  T. Glisovic,et al.  RNA‐binding proteins and post‐transcriptional gene regulation , 2008, FEBS letters.

[17]  J. A. Steitz,et al.  HuR and mRNA stability , 2001, Cellular and Molecular Life Sciences CMLS.

[18]  A. Correspondent Translational repression , 2020, Nature.

[19]  G. M. Wilson,et al.  Phosphorylation of p40AUF1 Regulates Binding to A + U-rich mRNA-destabilizing Elements and Protein-induced Changes in Ribonucleoprotein Structure* , 2003, Journal of Biological Chemistry.

[20]  S. Srikantan,et al.  Ubiquitin‐mediated proteolysis of HuR by heat shock , 2009, The EMBO journal.

[21]  P. Blackshear,et al.  Identification of a Major Phosphopeptide in Human Tristetraprolin by Phosphopeptide Mapping and Mass Spectrometry , 2014, PloS one.

[22]  F. Allain,et al.  RRM-RNA recognition: NMR or crystallography…and new findings. , 2013, Current opinion in structural biology.

[23]  Ching-Jin Chang,et al.  Regulation of tristetraprolin during differentiation of 3T3‐L1 preadipocytes , 2007, The FEBS journal.

[24]  P. King,et al.  Novel DNA-binding properties of the RNA-binding protein TIAR , 2005, Nucleic Acids Research.

[25]  J. Saklatvala,et al.  The Stability of Tristetraprolin mRNA Is Regulated by Mitogen-activated Protein Kinase p38 and by Tristetraprolin Itself* , 2004, Journal of Biological Chemistry.

[26]  Xiaowen Zhang,et al.  Amyotrophic Lateral Sclerosis-linked Mutant SOD1 Sequesters Hu Antigen R (HuR) and TIA-1-related Protein (TIAR) , 2009, The Journal of Biological Chemistry.

[27]  Shelly C. Lu,et al.  Murine double minute 2 regulates Hu antigen R stability in human liver and colon cancer through NEDDylation , 2012, Hepatology.

[28]  J. Stévenin,et al.  TIA-1 and TIAR Activate Splicing of Alternative Exons with Weak 5′ Splice Sites followed by a U-rich Stretch on Their Own Pre-mRNAs* , 2001, The Journal of Biological Chemistry.

[29]  A. Shyu,et al.  Versatile Role for hnRNP D Isoforms in the Differential Regulation of Cytoplasmic mRNA Turnover , 2001, Molecular and Cellular Biology.

[30]  B. Vojtesek,et al.  The role of the 3' untranslated region in post-transcriptional regulation of protein expression in mammalian cells. , 2012, RNA biology.

[31]  Michael Briese,et al.  iCLIP Predicts the Dual Splicing Effects of TIA-RNA Interactions , 2010, PLoS biology.

[32]  N. Barbosa-Morais,et al.  Alternative splicing: the pledge, the turn, and the prestige , 2017, Human Genetics.

[33]  Olivia S. Rissland The organization and regulation of mRNA–protein complexes , 2016, Wiley interdisciplinary reviews. RNA.

[34]  L. Regan,et al.  Structure and function of KH domains , 2008, The FEBS journal.

[35]  P. Blackshear,et al.  HuR as a negative posttranscriptional modulator in inflammation. , 2005, Molecular cell.

[36]  G. Brewer,et al.  An A + U-rich element RNA-binding factor regulates c-myc mRNA stability in vitro , 1991, Molecular and cellular biology.

[37]  D. Kerr,et al.  Alternative splicing of TIA‐1 in human colon cancer regulates VEGF isoform expression, angiogenesis, tumour growth and bevacizumab resistance , 2014, Molecular oncology.

[38]  K. Mahtani,et al.  The 3′ Untranslated Region of Tumor Necrosis Factor Alpha mRNA Is a Target of the mRNA-Stabilizing Factor HuR , 2001, Molecular and Cellular Biology.

[39]  W. Seeger,et al.  TIAR and TIA-1 mRNA-binding proteins co-aggregate under conditions of rapid oxygen decline and extreme hypoxia and suppress the HIF-1α pathway. , 2010, Journal of molecular cell biology.

[40]  E. Marcotte,et al.  Insights into the regulation of protein abundance from proteomic and transcriptomic analyses , 2012, Nature Reviews Genetics.

[41]  G. M. Wilson,et al.  Folding of A+U-rich RNA Elements Modulates AUF1 Binding , 2001, The Journal of Biological Chemistry.

[42]  M. Gorospe,et al.  Translational Control of Cytochrome c by RNA-Binding Proteins TIA-1 and HuR , 2006, Molecular and Cellular Biology.

[43]  T. Ishii,et al.  Role of Auf1 in elimination of oxidatively damaged messenger RNA in human cells. , 2015, Free radical biology & medicine.

[44]  M. Gorospe,et al.  Translational Repression by RNA-Binding Protein TIAR , 2006, Molecular and Cellular Biology.

[45]  M. Gorospe,et al.  Analysis of Turnover and Translation Regulatory RNA-Binding Protein Expression through Binding to Cognate mRNAs , 2007, Molecular and Cellular Biology.

[46]  Matthew Brook,et al.  Mitogen-Activated Protein Kinase-Activated Protein Kinase 2 Regulates Tumor Necrosis Factor mRNA Stability and Translation Mainly by Altering Tristetraprolin Expression, Stability, and Binding to Adenine/Uridine-Rich Element , 2006, Molecular and Cellular Biology.

[47]  Maria Carmo-Fonseca,et al.  The rules and roles of nucleocytoplasmic shuttling proteins , 2001, FEBS letters.

[48]  David Fernández-Ramos,et al.  NEDDylation in liver cancer: The regulation of the RNA binding protein Hu antigen R. , 2015, Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.].

[49]  Markus Blatter,et al.  RNA recognition motifs: boring? Not quite. , 2008, Current opinion in structural biology.

[50]  Hilla Peretz,et al.  Ju n 20 03 Schrödinger ’ s Cat : The rules of engagement , 2003 .

[51]  A. Levy,et al.  A 40-bp RNA Element That Mediates Stabilization of Vascular Endothelial Growth Factor mRNA by HuR* , 2002, The Journal of Biological Chemistry.

[52]  P. Anderson,et al.  TIA‐1 is a translational silencer that selectively regulates the expression of TNF‐α , 2000 .

[53]  A. Shyu,et al.  RNA stabilization by the AU‐rich element binding protein, HuR, an ELAV protein , 1998, The EMBO journal.

[54]  P. Anderson,et al.  Posttranscriptional mechanisms regulating the inflammatory response. , 2006, Advances in immunology.

[55]  A. Díaz-Quintana,et al.  Dimerization model of the C‐terminal RNA Recognition Motif of HuR , 2015, FEBS letters.

[56]  F. Blanco,et al.  The C-terminal RNA binding motif of HuR is a multi-functional domain leading to HuR oligomerization and binding to U-rich RNA targets , 2014, RNA biology.

[57]  L. Paillard,et al.  AU-rich elements and associated factors: are there unifying principles? , 2006, Nucleic acids research.

[58]  Kevin J Luebke,et al.  Faculty Opinions recommendation of The RNA-binding protein KSRP promotes the biogenesis of a subset of microRNAs. , 2009 .

[59]  J. Malter,et al.  Regulation of AU-Rich Element RNA Binding Proteins by Phosphorylation and the Prolyl Isomerase Pin1 , 2015, Biomolecules.

[60]  A. Shyu,et al.  Highly Selective Actions of HuR in Antagonizing AU-Rich Element-Mediated mRNA Destabilization , 2002, Molecular and Cellular Biology.

[61]  G. Delsol,et al.  HuR-Mediated Control of C/EBPβ mRNA Stability and Translation in ALK-Positive Anaplastic Large Cell Lymphomas , 2011, Molecular Cancer Research.

[62]  D. Aswad,et al.  Lipopolysaccharide-induced Methylation of HuR, an mRNA-stabilizing Protein, by CARM1* , 2002, The Journal of Biological Chemistry.

[63]  Gary Brewer,et al.  Regulation of Cyclooxygenase 2 mRNA Stability by the Mitogen-Activated Protein Kinase p38 Signaling Cascade , 2000, Molecular and Cellular Biology.

[64]  V. Kruys,et al.  AU-rich element-mediated translational control: complexity and multiple activities of trans-activating factors. , 2001, Biochemical Society transactions.

[65]  M. Gorospe,et al.  TIA-1 RRM23 binding and recognition of target oligonucleotides , 2017, Nucleic acids research.

[66]  S. Srikantan,et al.  HuR recruits let-7/RISC to repress c-Myc expression. , 2009, Genes & development.

[67]  G. Brewer,et al.  The role of AUF1 in regulated mRNA decay , 2010, Wiley interdisciplinary reviews. RNA.

[68]  John D. Venable,et al.  Identification of the anti-inflammatory protein tristetraprolin as a hyperphosphorylated protein by mass spectrometry and site-directed mutagenesis. , 2006, The Biochemical journal.

[69]  Geoff Kelly,et al.  Phosphorylation-mediated unfolding of a KH domain regulates KSRP localization via 14-3-3 binding , 2009, Nature Structural &Molecular Biology.

[70]  A. Ramos,et al.  The structure of the C-terminal KH domains of KSRP reveals a noncanonical motif important for mRNA degradation. , 2007, Structure.

[71]  Ranjit Prasad Bahadur,et al.  A structural perspective of RNA recognition by intrinsically disordered proteins , 2016, Cellular and Molecular Life Sciences.

[72]  H. Shibata,et al.  KSRP/FUBP2 Is a Binding Protein of GO-Y086, a Cytotoxic Curcumin Analogue. , 2010, ACS medicinal chemistry letters.

[73]  J. Valcárcel,et al.  Fas-activated Serine/Threonine Kinase (FAST K) Synergizes with TIA-1/TIAR Proteins to Regulate Fas Alternative Splicing* , 2007, Journal of Biological Chemistry.

[74]  I. Díaz-Moreno,et al.  RNA Binding of T-cell Intracellular Antigen-1 (TIA-1) C-terminal RNA Recognition Motif Is Modified by pH Conditions* , 2013, The Journal of Biological Chemistry.

[75]  L. Sandell,et al.  Nuclear Protein TIA-1 Regulates COL2A1 Alternative Splicing and Interacts with Precursor mRNA and Genomic DNA* , 2007, Journal of Biological Chemistry.

[76]  Young Woo Park,et al.  Tristetraprolin regulates expression of VEGF and tumorigenesis in human colon cancer , 2010, International journal of cancer.

[77]  B. K. Thakur,et al.  Functional Analysis of KSRP Interaction with the AU-Rich Element of Interleukin-8 and Identification of Inflammatory mRNA Targets , 2007, Molecular and Cellular Biology.

[78]  E. K. Lee Post-translational modifications of RNA-binding proteins and their roles in RNA granules. , 2012, Current protein and peptide science.

[79]  M. Karin,et al.  A KH domain RNA binding protein, KSRP, promotes ARE-directed mRNA turnover by recruiting the degradation machinery. , 2004, Molecular cell.

[80]  G. M. Wilson,et al.  Different modes of interaction by TIAR and HuR with target RNA and DNA , 2011, Nucleic acids research.

[81]  K. Khabar,et al.  Alternative polyadenylation variants of the RNA binding protein, HuR: abundance, role of AU-rich elements and auto-Regulation , 2009, Nucleic acids research.

[82]  J. M. Izquierdo,et al.  Two Isoforms of the T-cell Intracellular Antigen 1 (TIA-1) Splicing Factor Display Distinct Splicing Regulation Activities , 2007, Journal of Biological Chemistry.

[83]  J. Steitz,et al.  Overexpression of HuR, a nuclear–cytoplasmic shuttling protein, increases the in vivo stability of ARE‐containing mRNAs , 1998, The EMBO journal.

[84]  P. Blackshear,et al.  Interactions of CCCH Zinc Finger Proteins with mRNA , 2001, The Journal of Biological Chemistry.

[85]  K. Khabar,et al.  The AU-rich transcriptome: more than interferons and cytokines, and its role in disease. , 2005, Journal of interferon & cytokine research : the official journal of the International Society for Interferon and Cytokine Research.

[86]  A. Morrison,et al.  The Proximal Region of the 3′-Untranslated Region of Cyclooxygenase-2 is Recognized by a Multimeric Protein Complex Containing HuR, TIA-1, TIAR, and the Heterogeneous Nuclear Ribonucleoprotein U* , 2003, Journal of Biological Chemistry.

[87]  P. Anderson,et al.  Regulation of Cyclooxygenase-2 Expression by the Translational Silencer TIA-1 , 2003, The Journal of experimental medicine.

[88]  M. Gorospe,et al.  Identification of a target RNA motif for RNA-binding protein HuR. , 2004, Proceedings of the National Academy of Sciences of the United States of America.

[89]  K. Duff,et al.  Contrasting Pathology of the Stress Granule Proteins TIA-1 and G3BP in Tauopathies , 2012, The Journal of Neuroscience.

[90]  G. Brewer,et al.  Competitive binding of AUF1 and TIAR to MYC mRNA controls its translation , 2007, Nature Structural &Molecular Biology.

[91]  A. Ramos,et al.  Orientation of the central domains of KSRP and its implications for the interaction with the RNA targets , 2010, Nucleic acids research.

[92]  G. M. Wilson,et al.  Structural Remodeling of an A + U-rich RNA Element by Cation or AUF1 Binding* , 2001, The Journal of Biological Chemistry.

[93]  Susan Jones,et al.  Evaluating conformational changes in protein structures binding RNA , 2007, Proteins.

[94]  M. Gorospe,et al.  The binding of TIA-1 to RNA C-rich sequences is driven by its C-terminal RRM domain , 2014, RNA biology.

[95]  Manfred Auer,et al.  The x-ray crystal structure of the first RNA recognition motif and site-directed mutagenesis suggest a possible HuR redox sensing mechanism. , 2010, Journal of molecular biology.

[96]  R. Robey,et al.  AUF1/hnRNP D represses expression of VEGF in macrophages , 2012, Molecular biology of the cell.

[97]  T. Hla,et al.  The RNA-binding Protein HuR Regulates the Expression of Cyclooxygenase-2* , 2003, Journal of Biological Chemistry.

[98]  Georges Huez,et al.  Identification of TIAR as a Protein Binding to the Translational Regulatory AU-rich Element of Tumor Necrosis Factor α mRNA* , 1999, The Journal of Biological Chemistry.

[99]  A. Levy,et al.  Hypoxic Stabilization of Vascular Endothelial Growth Factor mRNA by the RNA-binding Protein HuR* , 1998, The Journal of Biological Chemistry.

[100]  G. M. Wilson,et al.  Alternatively Expressed Domains of AU-rich Element RNA-binding Protein 1 (AUF1) Regulate RNA-binding Affinity, RNA-induced Protein Oligomerization, and the Local Conformation of Bound RNA Ligands* , 2010, The Journal of Biological Chemistry.

[101]  A. Velázquez‐Campoy,et al.  A Non-Invasive NMR Method Based on Histidine Imidazoles to Analyze the pH-Modulation of Protein-Nucleic Acid Interfaces. , 2015, Chemistry.

[102]  G. M. Wilson,et al.  Structure and genomic organization of the human AUF1 gene: alternative pre-mRNA splicing generates four protein isoforms. , 1998, Genomics.