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A Perspective on the Role of microRNA-128 Regulation in Mental and Behavioral Disorders

Ching, Ai-Sze, Ahmad-Annuar, Azlina·2015·Frontiers in Cellular Neuroscience

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Crossref · 10.3389/fncel.2015.00465

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FIGURE 1 (A) The Venn diagram shows the number of miR-128 target genes as identified by Tan et al. (2013) TargetScan and published targets. Total number of genes that are shared between Tan et al. (2013) and TargetScan is 214 genes; 34 genes are shared by TargetScan and our list of published miR-128 targets. (B) Top 10 functional clusters of miR-128 target genes as classified by DAVID bioinformatics tool. Using the mouse genome as the background, the threshold was set at the following criteria: classification stringency = highest; maximum EASE score = 0.05. EASE score is a modified Fisher Exact p value which range from 0 to 1, with 0 shows perfect enrichment. (C) Biological pathways (KEGG database) shared by miR-128 target genes as annotated by the KEGG pathway database. Using the mouse genome as background, the threshold was set at the following criteria: minimum number of genes for the corresponding pathway = 2; maximum EASE score = 0.05.
FIGURE 1 (A) The Venn diagram shows the number of miR-128 target genes as identified by Tan et al. (2013) TargetScan and published targets. Total number of genes that are shared between Tan et al. (2013) and TargetScan is 214 genes; 34 genes are shared by TargetScan and our list of published miR-128 targets. (B) Top 10 functional clusters of miR-128 target genes as classified by DAVID bioinformatics tool. Using the mouse genome as the background, the threshold was set at the following criteria: classification stringency = highest; maximum EASE score = 0.05. EASE score is a modified Fisher Exact p value which range from 0 to 1, with 0 shows perfect enrichment. (C) Biological pathways (KEGG database) shared by miR-128 target genes as annotated by the KEGG pathway database. Using the mouse genome as background, the threshold was set at the following criteria: minimum number of genes for the corresponding pathway = 2; maximum EASE score = 0.05.CC BY · PubMed Central

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Research works printed but not linked: 73

  1. Adlakha, 2011, MicroRNA-128 downregulates Bax and induces apoptosis in human embryonic kidney cells., Cell. Mol. Life Sci., 68, 1415, 10.1007/s00018-010-0528-y · DOI
  2. Ando, 2013, Calmodulin-dependent regulation of neurotransmitter release differs in subsets of neuronal cells., Brain Res., 1535, 1, 10.1016/j.brainres.2013.08.018 · DOI
  3. Azzam, 2013, CSF1 is a novel p53 target gene whose protein product functions in a feed-forward manner to suppress apoptosis and enhance p53-mediated growth arrest., PLoS ONE, 8, 10.1371/journal.pone.0074297 · DOI
  4. Bartel, 2009, MicroRNAs: target recognition and regulatory functions., Cell, 136, 215, 10.1016/j.cell.2009.01.002 · DOI · Paper page
  5. Beveridge, 2010, Schizophrenia is associated with an increase in cortical microRNA biogenesis., Mol. Psychiatry, 15, 1176, 10.1038/mp.2009.84 · DOI
  6. Bruno, 2011, Identification of a microRNA that activates gene expression by repressing nonsense-mediated RNA decay., Mol. Cell, 42, 500, 10.1016/j.molcel.2011.04.018 · DOI
  7. Cao, 2012, Bmi-1 absence causes premature brain degeneration., PLoS ONE, 7, 10.1371/journal.pone.0032015 · DOI
  8. Caporaso, 2000, Drugs of abuse modulate the phosphorylation of ARPP-21, a cyclic AMP-regulated phosphoprotein enriched in the basal ganglia., Neuropharmacology, 39, 1637, 10.1016/S0028-3908(99)00230-0 · DOI
  9. Chang, 2007, The nonsense-mediated decay RNA surveillance pathway., Annu. Rev. Biochem., 76, 51, 10.1146/annurev.biochem.76.050106.093909 · DOI
  10. Chazal, 2013, EJC core component MLN51 interacts with eIF3 and activates translation., Proc. Natl. Acad. Sci. U.S.A., 110, 5903, 10.1073/pnas.1218732110 · DOI
  11. Cohen, 2008, Doublecortin supports the development of dendritic arbors in primary hippocampal neurons., Dev. Neurosci., 30, 187, 10.1159/000109862 · DOI
  12. Davis, 2012, Regulator of calmodulin signaling knockout mice display anxiety-like behavior and motivational deficits., Eur. J. Neurosci., 35, 300, 10.1111/j.1460-9568.2011.07956.x · DOI
  13. Dynan, 1983, The promoter-specific transcription factor Sp1 binds to upstream sequences in the SV40 early promoter., Cell, 35, 79, 10.1016/0092-8674(83)90210-6 · DOI · Paper page
  14. Evangelisti, 2009, MiR-128 up-regulation inhibits Reelin and DCX expression and reduces neuroblastoma cell motility and invasiveness., FASEB J., 23, 4276, 10.1096/fj.09-134965 · DOI · Paper page
  15. Fatemi, 2005, Reelin signaling is impaired in autism., Biol. Psychiatry, 57, 777, 10.1016/j.biopsych.2004.12.018 · DOI · Paper page
  16. Frotscher, 2009, Role of Reelin in the development and maintenance of cortical lamination., J. Neural Transm., 116, 1451, 10.1007/s00702-009-0228-7 · DOI
  17. Gates, 2006, Re-examining the ontogeny of substantia nigra dopamine neurons., Eur. J. Neurosci., 23, 1384, 10.1111/j.1460-9568.2006.04637.x · DOI
  18. Gentili, 2005, Cholesterol secretion and homeostasis in chondrocytes: a liver X receptor and retinoid X receptor heterodimer mediates apolipoprotein A1 expression., Matrix Biol., 24, 35, 10.1016/j.matbio.2004.12.003 · DOI
  19. Germain, 2013, Doublecortin knockout mice show normal hippocampal-dependent memory despite CA3 lamination defects., PLoS ONE, 8, 10.1371/journal.pone.0074992 · DOI
  20. Guidotti, 2000, Decrease in reelin and glutamic acid decarboxylase67 (GAD67) expression in schizophrenia and bipolar disorder: a postmortem brain study., Arch. Gen. Psychiatry, 57, 1061, 10.1001/archpsyc.57.11.1061 · DOI
  21. Han, 2012, Changes in insulin-signaling transduction pathway underlie learning/memory deficits in an Alzheimer’s disease rat model., J. Neural Transm., 119, 1407, 10.1007/s00702-012-0803-1 · DOI
  22. Herring, 2012, Reelin depletion is an early phenomenon of Alzheimer’s pathology., J. Alzheimers Dis., 30, 963, 10.3233/JAD-2012-112069 · DOI · Paper page
  23. Huang, 2009, Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources., Nat. Protoc., 4, 44, 10.1038/nprot.2008.211 · DOI · Paper page
  24. Jang, 2013, Identification of DCX gene mutation in lissencephaly spectrum with subcortical band heterotopia using whole exome sequencing., Pediatr. Neurol., 48, 411, 10.1016/j.pediatrneurol.2012.12.033 · DOI
  25. Karam, 2012, A conserved microRNA/NMD regulatory circuit controls gene expression., RNA Biol., 9, 22, 10.4161/rna.9.1.18010 · DOI
  26. Kim, 2004, Identification of many microRNAs that copurify with polyribosomes in mammalian neurons., Proc. Natl. Acad. Sci. U.S.A., 101, 360, 10.1073/pnas.2333854100 · DOI
  27. Koie, 2014, Cleavage within Reelin repeat 3 regulates the duration and range of the signaling activity of Reelin protein., J. Biol. Chem., 289, 12922, 10.1074/jbc.M113.536326 · DOI
  28. Koizumi, 2006, Doublecortin-like kinase functions with doublecortin to mediate fiber tract decussation and neuronal migration., Neuron, 49, 55, 10.1016/j.neuron.2005.10.040 · DOI
  29. Kolsch, 2009, RXRA gene variations influence Alzheimer’s disease risk and cholesterol metabolism., J. Cell. Mol. Med., 13, 589, 10.1111/j.1582-4934.2009.00383.x · DOI
  30. Kuang, 2011, A new single-nucleotide mutation (rs362719) of the reelin (RELN) gene associated with schizophrenia in female Chinese Han., Genet. Mol. Res., 10, 1650, 10.4238/vol10-3gmr1343 · DOI
  31. Kunde, 2013, Characterisation of de novo MAPK10/JNK3 truncation mutations associated with cognitive disorders in two unrelated patients., Hum. Genet., 132, 461, 10.1007/s00439-012-1260-5 · DOI
  32. Laske, 2010, Macrophage colony-stimulating factor (M-CSF) in plasma and CSF of patients with mild cognitive impairment and Alzheimer’s disease., Curr. Alzheimer Res., 7, 409, 10.2174/156720510791383813 · DOI
  33. Lee, 2010, Genetic copy number variants in sib pairs both affected with schizophrenia., J. Biomed. Sci., 17, 10.1186/1423-0127-17-2 · DOI
  34. Lee, 2009, New class of microRNA targets containing simultaneous 5′-UTR and 3′-UTR interaction sites., Genome Res., 19, 1175, 10.1101/gr.089367.108 · DOI
  35. Leung, 2004, Bmi1 is essential for cerebellar development and is overexpressed in human medulloblastomas., Nature, 428, 337, 10.1038/nature02385 · DOI
  36. Lewis, 2005, Conserved seed pairing, often flanked by adenosines, indicates that thousands of human genes are microRNA targets., Cell, 120, 15, 10.1016/j.cell.2004.12.035 · DOI · Paper page
  37. Li, 2013, miR-128 and its target genes in tumorigenesis and metastasis., Exp. Cell Res., 319, 3059, 10.1016/j.yexcr.2013.07.031 · DOI
  38. Lin, 2011, The brain-specific microRNA miR-128b regulates the formation of fear-extinction memory., Nat. Neurosci., 14, 1115, 10.1038/nn.2891 · DOI · Paper page
  39. Mao, 2009, Unique aspects of transcriptional regulation in neurons–nuances in NFkappaB and Sp1-related factors., J. Neuroinflammation, 6, 10.1186/1742-2094-6-16 · DOI
  40. Mao, 2014, Serum miR-21 is a diagnostic and prognostic marker of primary central nervous system lymphoma., Neurol. Sci., 35, 233, 10.1007/s10072-013-1491-9 · DOI
  41. Marangi, 2013, Interstitial deletion of 3p22.3p22.2 encompassing ARPP21 and CLASP2 is a potential pathogenic factor for a syndromic form of intellectual disability: a co-morbidity model with additional copy number variations in a large family., Am. J. Med. Genet. A, 161A, 2890, 10.1002/ajmg.a.36257 · DOI
  42. Megraw, 2010, Isoform specific gene auto-regulation via miRNAs: a case study on miR-128b and ARPP-21., Theor. Chem. Acc., 125, 593, 10.1007/s00214-009-0647-4 · DOI
  43. Mohit, 1995, p493F12 kinase: a novel MAP kinase expressed in a subset of neurons in the human nervous system., Neuron, 14, 67, 10.1016/0896-6273(95)90241-4 · DOI
  44. Moores, 2006, Distinct roles of doublecortin modulating the microtubule cytoskeleton., EMBO J., 25, 4448, 10.1038/sj.emboj.7601335 · DOI
  45. Nosten-Bertrand, 2008, Epilepsy in Dcx knockout mice associated with discrete lamination defects and enhanced excitability in the hippocampus., PLoS ONE, 3, 10.1371/journal.pone.0002473 · DOI
  46. Ouimet, 1989, ARPP-21, a cyclic AMP-regulated phosphoprotein enriched in dopamine-innervated brain regions. II. Immunocytochemical localization in rat brain., J. Neurosci., 9, 5
  47. Ovadia, 2011, The genetic variation of RELN expression in schizophrenia and bipolar disorder., PLoS ONE, 6, 10.1371/journal.pone.0019955 · DOI
  48. Oyler, 1989, The identification of a novel synaptosomal-associated protein, SNAP-25, differentially expressed by neuronal subpopulations., J. Cell Biol., 109, 3039, 10.1083/jcb.109.6.3039 · DOI
  49. Papagiannakopoulos, 2012, Pro-neural miR-128 is a glioma tumor suppressor that targets mitogenic kinases., Oncogene, 31, 1884, 10.1038/onc.2011.380 · DOI · Paper page
  50. Paschou, 2012, Neurofibromin 1 is a miRNA target in neurons., PLoS ONE, 7, 10.1371/journal.pone.0046773 · DOI
  51. Patrylo, 2006, Reeler homozygous mice exhibit enhanced susceptibility to epileptiform activity., Epilepsia, 47, 257, 10.1111/j.1528-1167.2006.00417.x · DOI
  52. Perkins, 2007, microRNA expression in the prefrontal cortex of individuals with schizophrenia and schizoaffective disorder., Genome Biol., 8, 10.1186/gb-2007-8-2-r27 · DOI · Paper page
  53. Pore, 2004, Sp1 is involved in Akt-mediated induction of VEGF expression through an HIF-1-independent mechanism., Mol. Biol. Cell, 15, 4841, 10.1091/mbc.E04-05-0374 · DOI
  54. Qian, 2012, Loss of SNAIL regulated miR-128-2 on chromosome 3p22.3 targets multiple stem cell factors to promote transformation of mammary epithelial cells., Cancer Res., 72, 6036, 10.1158/0008-5472.CAN-12-1507 · DOI
  55. Qiu, 2006, Cognitive disruption and altered hippocampus synaptic function in Reelin haploinsufficient mice., Neurobiol. Learn. Mem., 85, 228, 10.1016/j.nlm.2005.11.001 · DOI · Paper page
  56. Rakhilin, 2004, A network of control mediated by regulator of calcium/calmodulin-dependent signaling., Science, 306, 698, 10.1126/science.1099961 · DOI
  57. Reinecke, 2013, Knockout of c-Jun N-terminal kinases 1, 2 or 3 isoforms induces behavioural changes., Behav. Brain Res., 245, 88, 10.1016/j.bbr.2013.02.013 · DOI
  58. Shoichet, 2006, Truncation of the CNS-expressed JNK3 in a patient with a severe developmental epileptic encephalopathy., Hum. Genet., 118, 559, 10.1007/s00439-005-0084-y · DOI
  59. Sollner, 1993, SNAP receptors implicated in vesicle targeting and fusion., Nature, 362, 318, 10.1038/362318a0 · DOI
  60. Stelzer, 2011, In-silico human genomics with GeneCards., Hum. Genomics, 5, 709, 10.1186/1479-7364-5-6-709 · DOI
  61. Tan, 2013, MicroRNA-128 governs neuronal excitability and motor behavior in mice., Science, 342, 1254, 10.1126/science.1244193 · DOI · Paper page
  62. Tararuk, 2006, JNK1 phosphorylation of SCG10 determines microtubule dynamics and axodendritic length., J. Cell Biol., 173, 265, 10.1083/jcb.200511055 · DOI
  63. Teixeira, 2011, Overexpression of Reelin prevents the manifestation of behavioral phenotypes related to schizophrenia and bipolar disorder., Neuropsychopharmacology, 36, 2395, 10.1038/npp.2011.153 · DOI
  64. Thompson, 2003, SNAP-25 reduction in the hippocampus of patients with schizophrenia., Prog. Neuropsychopharmacol. Biol. Psychiatry, 27, 411, 10.1016/S0278-5846(03)00027-7 · DOI
  65. Walaas, 1983, Regional distribution of calcium– and cyclic adenosine 3’:5’-monophosphate-regulated protein phosphorylation systems in mammalian brain. II. Soluble systems., J. Neurosci., 3, 302, 10.1523/JNEUROSCI.03-02-00302.1983 · DOI
  66. Wang, 2012, Sp1 regulates human huntingtin gene expression., J. Mol. Neurosci., 47, 311, 10.1007/s12031-012-9739-z · DOI
  67. Weiss, 2008, EGFR regulation by microRNA in lung cancer: correlation with clinical response and survival to gefitinib and EGFR expression in cell lines., Ann. Oncol., 19, 1053, 10.1093/annonc/mdn006 · DOI
  68. Williams, 1989, ARPP-refvol21, a cyclic AMP-regulated phosphoprotein enriched in dopamine-innervated brain regions. I. Amino acid sequence of ARPP-21B from bovine caudate nucleus., J. Neurosci., 9, 3631, 10.1523/JNEUROSCI.09-10-03631.1989 · DOI
  69. Wu, 2014, MicroRNA-128 regulates the differentiation of rat bone mesenchymal stem cells into neuron-like cells by Wnt signaling., Mol. Cell. Biochem., 387, 151, 10.1007/s11010-013-1880-7 · DOI
  70. Xu, 2013, SNARE proteins synaptobrevin, SNAP-25, and syntaxin are involvedin rapid and slow endocytosis at synapses., Cell Rep., 3, 1414, 10.1016/j.celrep.2013.03.010 · DOI
  71. Yap, 2012, Doublecortin (DCX) mediates endocytosis of neurofascin independently of microtubule binding., J. Neurosci., 32, 7439, 10.1523/JNEUROSCI.5318-11.2012 · DOI · Paper page
  72. Zare, 2015, A novel protocol to differentiate induced pluripotent stem cells by neuronal microRNAs to provide a suitable cellular model., Chem. Biol. Drug Des., 86, 232, 10.1111/cbdd.12485 · DOI
  73. Zencak, 2005, Bmi1 loss produces an increase in astroglial cells and a decrease in neural stem cell population and proliferation., J. Neurosci., 25, 5774, 10.1523/JNEUROSCI.3452-04.2005 · DOI

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Authors
Ching, A.-S., & Ahmad-Annuar, A.
Venue
Frontiers in Cellular Neuroscience
Published
2015-12-14
Volume
9
ISSN
1662-5102
Cited by
24
References
8
Funders
  • Ministry of Higher Education, Malaysia (MOHE-HIR-E29)
  • Universiti Malaya (RG399/12HTM)

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