MECP2 and associated Rett syndrome (WP3584)
Homo sapiens
MECP2 (methyl-CpG binding protein 2) is in many mammals an important regulator of neuronal function and development. It affects all cell types, especially neurons but also astrocytes, oligodendrocytes, and glial cells. MECP2 plays an important role in neuronal differentiation, maturation, morphology and function and influences synaptic plasticity. Mutations impairing the proper function of MECP2 are mainly associated with the Rett syndrome but may also contribute to other neurological disorders like schizophrenia, FASD (fetal alcohol syndrome), PPM-X-syndrome, autism, Prader-Will-syndrome, and Angelman-syndrome. Dependant on the cofactors MECP2 acts as an activator or repressor of transcription and micro RNA production. It affects RNA splicing and regulates chromatin structure together with HP1 and interferes in methylation of DNA (epigenetics). The expression of MECP2 itself is highly regulated by promotor elements, cis-regulatory elements, polyadenylation, promotor DNA methylation and miRNA. Please cite this pathways as: http://www.wikipathways.org/instance/WP3584 Ehrhart et al. 2016 https://doi.org/10.1186/s13023-016-0545-5 - the pathway version in the paper is 90609. Proteins on this pathway have targeted assays available via the [https://assays.cancer.gov/available_assays?wp_id=WP3584 CPTAC Assay Portal]
Authors
Friederike Ehrhart , Egon Willighagen , Kristina Hanspers , Ryan Miller , Martina Summer-Kutmon , Alex Pico , Lauren J. Dupuis , and Eric WeitzActivity
Discuss this pathway
Check for ongoing discussions or start your own.
Cited In
- Understanding signaling and metabolic paths using semantified and harmonized information about biological interactions (2022).
- Genetic Landscape of Rett Syndrome Spectrum: Improvements and Challenges (2019).
- Rett syndrome – biological pathways leading from MECP2 to disorder phenotypes (2016).
Are you planning to include this pathway in your next publication? See How to Cite and add a link here to your paper once it's online.
Organisms
Homo sapiensCommunities
Diseases Rare DiseasesAnnotations
Disease Ontology
Rett syndromePathway Ontology
disease pathwayCell Type Ontology
oligodendrocyte microglial cell astrocyteLabel | Type | Compact URI | Comment |
---|---|---|---|
Dopamine | Metabolite | hmdb:HMDB0000073 | |
GABA | Metabolite | chebi:16865 | |
Glycine | Metabolite | hmdb:HMDB0000123 | |
Norepinephrine | Metabolite | hmdb:HMDB0000216 | |
NMDA | Metabolite | hmdb:HMDB0002393 | N-Methyl-D-aspartic acid |
Glutamate | Metabolite | chebi:29987 | |
Serotonin | Metabolite | hmdb:HMDB0000259 | |
Trofinetide | Metabolite | pubchem.compound:11318905 | |
Melatonin | Metabolite | hmdb:HMDB0001389 | |
Myoinositol | Metabolite | hmdb:HMDB0000211 | |
D-serine | Metabolite | chebi:16523 | |
NCOR1 | GeneProduct | ensembl:ENSG00000141027 | nuclear receptor co-repressor 1 |
MYT1 | GeneProduct | ensembl:ENSG00000196132 | myelin transcription factor 1proof of Mecp2 inhibition in Oligodendrocytes |
BRN3 | GeneProduct | ensembl:ENSG00000152192 | POU domain, class 4, transcription factor 1 |
DLX5 | GeneProduct | ensembl:ENSG00000105880 | |
MTOR | GeneProduct | ensembl:ENSG00000198793 | |
APOC2 | GeneProduct | ensembl:ENSG00000234906 | apolipoprotein C-II |
HDAC1 | GeneProduct | ensembl:ENSG00000116478 | |
BDNF | GeneProduct | ensembl:ENSG00000176697 | brain derived neurotrophic factor |
SST | GeneProduct | ensembl:ENSG00000157005 | Somatostatin |
NREP | GeneProduct | ensembl:ENSG00000134986 | neuronal regeneration related protein |
TET3 | GeneProduct | ensembl:ENSG00000187605 | |
MECP2 | GeneProduct | ensembl:ENSG00000169057 | methyl CpG binding protein 2 |
BRN2 | GeneProduct | ensembl:ENSG00000184486 | POU domain, class 3, transcription factor 2 |
DLX6 | GeneProduct | ensembl:ENSG00000006377 | |
SMC3 | GeneProduct | ensembl:ENSG00000108055 | tructural maintenance of chromosomes 3 |
MEF2C | GeneProduct | ensembl:ENSG00000081189 | myocyte enhancer factor 2C |
TAP1 | GeneProduct | ensembl:ENSG00000168394 | transporter 1, ATP-binding cassette, sub-family B (MDR/TAP) |
UBE3A | GeneProduct | ensembl:ENSG00000114062 | |
RBFOX1 | GeneProduct | ensembl:ENSG00000078328 | ataxin 2 binding protein 1, Rbfox1 |
CNP | GeneProduct | ensembl:ENSG00000173786 | 2',3'-cyclic nucleotide 3' phosphodiesterase |
TET2 | GeneProduct | ensembl:ENSG00000168769 | |
SGK1 | GeneProduct | ensembl:ENSG00000118515 | |
FKBP5 | GeneProduct | ensembl:ENSG00000096060 | |
RPS6 | GeneProduct | ensembl:ENSG00000137154 | |
EZH2 | GeneProduct | ensembl:ENSG00000106462 | histone H3 lysine 27 methyltransferase |
GAMT | GeneProduct | ensembl:ENSG00000130005 | guanidinoacetate methyltransferase |
AKT1 | GeneProduct | ensembl:ENSG00000142208 | |
MPP1 | GeneProduct | ensembl:ENSG00000130830 | |
OPRK1 | GeneProduct | ensembl:ENSG00000082556 | opioid receptor, kappa 1 |
ARHGEF26 | GeneProduct | ensembl:ENSG00000114790 | Rho guanine nucleotide exchange factor (GEF) 26 |
SIN3A | GeneProduct | ensembl:ENSG00000169375 | |
IGF2 | GeneProduct | ensembl:ENSG00000167244 | |
SP1 | GeneProduct | ensembl:ENSG00000185591 | trans-acting transcription factor 1 |
GAD1 | GeneProduct | ensembl:ENSG00000128683 | |
TAF1 | GeneProduct | ensembl:ENSG00000147133 | TAF1 RNA polymerase II, TATA box binding protein (TBP)-associated factor |
HNRNPH1 | GeneProduct | ensembl:ENSG00000169045 | HNRNPH1 |
CSRP1 | GeneProduct | ensembl:ENSG00000159176 | cysteine and glycine-rich protein 1 |
GRID1 | GeneProduct | ensembl:ENSG00000182771 | |
CDON | GeneProduct | ensembl:ENSG00000064309 | cell adhesion molecule-related/down-regulated by oncogenes |
MYT1 | GeneProduct | ensembl:ENSG00000196132 | Myelin transcription factor 1 |
C/EBP | GeneProduct | ensembl:ENSG00000221869 | CCAAT/enhancer binding protein (Cebpd), delta |
CAMK2A | GeneProduct | ensembl:ENSG00000070808 | |
MBP | GeneProduct | ensembl:ENSG00000197971 | myelin basic protein |
BCL6 | GeneProduct | ensembl:ENSG00000113916 | B cell leukemia/lymphoma 6 |
GABRR2 | GeneProduct | ensembl:ENSG00000111886 | gamma-aminobutyric acid (GABA) C receptor, subunit rho 2 |
CTCF | GeneProduct | ensembl:ENSG00000102974 | CCCTC-binding factor |
SP3 | GeneProduct | ensembl:ENSG00000172845 | trans-acting transcription factor 3 |
PRPF3 | GeneProduct | ensembl:ENSG00000134748 | PRP3 pre-mRNA processing factor 3 homolog (yeast) |
E2F1 | GeneProduct | ensembl:ENSG00000101412 | E2F transcription factor 1 |
AMPA | GeneProduct | ensembl:ENSG00000155511 | Glutamate receptor |
REST | GeneProduct | ensembl:ENSG00000084093 | RE1-silencing transcription factorSilences Mecp2 in non-neuronal tissue |
MAG | GeneProduct | ensembl:ENSG00000105695 | myelin-associated glycoprotein |
GPRIN1 | GeneProduct | ensembl:ENSG00000169258 | G protein-regulated inducer of neurite outgrowth 1 |
TET1 | GeneProduct | ensembl:ENSG00000138336 | tet methylcytosine dioxygenase 1 |
IGF1R | GeneProduct | ensembl:ENSG00000140443 | |
HNRNPF | GeneProduct | ensembl:ENSG00000169813 | Hnrnpfheterogeneous nuclear ribonucleoprotein F |
YB1 | GeneProduct | ensembl:ENSG00000065978 | data obtained with human cell line and mouse primary tissueY box protein 1 |
CREB1 | GeneProduct | ensembl:ENSG00000118260 | |
IGF1 | GeneProduct | ensembl:ENSG00000017427 | Glutamate receptor |
FOXG1 | GeneProduct | ensembl:ENSG00000176165 | Glutamate receptor |
PTEN | GeneProduct | ensembl:ENSG00000171862 | |
DHX9 | GeneProduct | ensembl:ENSG00000135829 | binding to MECP2 confirmed in mice |
FUS | GeneProduct | ensembl:ENSG00000089280 | binding to MECP2 confirmed in mice |
HNRNPF | GeneProduct | ensembl:ENSG00000169813 | binding to MECP2 confirmed in micealso known as hnRNPH+F |
TARDBP | GeneProduct | ensembl:ENSG00000120948 | binding to MECP2 confirmed in micealso known as TDP-43 |
PSIP1 | GeneProduct | ensembl:ENSG00000164985 | binding to MECP2 confirmed in micealso known as LEDGF |
FUT8 | GeneProduct | ensembl:ENSG00000033170 | fucosyltransferase 8 |
FGF2 | GeneProduct | ensembl:ENSG00000138685 | fibroblast growth factor 2 |
GRIN1 | GeneProduct | ensembl:ENSG00000176884 | related to FASD (fetal alcohole spectrum disorder)NMDA receptor subunit: There are 8 different variants of NR1, produced by alternative splicing of GRIN1 |
FGF3 | GeneProduct | ensembl:ENSG00000186895 | fibroblast growth factor 3 |
FGF4 | GeneProduct | ensembl:ENSG00000075388 | |
FGF5 | GeneProduct | ensembl:ENSG00000138675 | |
NF1 | GeneProduct | ensembl:ENSG00000196712 | neurofibromatosis 1 |
DLX5 | GeneProduct | ensembl:ENSG00000105880 | distal-less homeobox 5controls GABA production |
GRIA1 | GeneProduct | ensembl:ENSG00000155511 | effect of MECP2 via LEDGF/PSIP1 influenced change of splice variants proven for miceSubpart of AMPAR receptor |
GRIA3 | GeneProduct | ensembl:ENSG00000125675 | effect of MECP2 via LEDGF/PSIP1 influenced change of splice variants proven for miceSubpart of AMPAR receptor |
GRIA4 | GeneProduct | ensembl:ENSG00000152578 | effect of MECP2 via LEDGF/PSIP1 influenced change of splice variants proven for miceSubpart of AMPAR receptor |
References
- Multiple signaling pathways of the insulin-like growth factor 1 receptor in protection from apoptosis. Peruzzi F, Prisco M, Dews M, Salomoni P, Grassilli E, Romano G, et al. Mol Cell Biol. 1999 Oct;19(10):7203–15. PubMed Europe PMC Scholia
- Regulation of RNA splicing by the methylation-dependent transcriptional repressor methyl-CpG binding protein 2. Young JI, Hong EP, Castle JC, Crespo-Barreto J, Bowman AB, Rose MF, et al. Proc Natl Acad Sci U S A. 2005 Dec 6;102(49):17551–8. PubMed Europe PMC Scholia
- Identification of cis-regulatory elements for MECP2 expression. Liu J, Francke U. Hum Mol Genet. 2006 Jun 1;15(11):1769–82. PubMed Europe PMC Scholia
- MicroRNA in schizophrenia: genetic and expression analysis of miR-130b (22q11). Burmistrova OA, Goltsov AY, Abramova LI, Kaleda VG, Orlova VA, Rogaev EI. Biochemistry (Mosc). 2007 May;72(5):578–82. PubMed Europe PMC Scholia
- MeCP2-dependent repression of an imprinted miR-184 released by depolarization. Nomura T, Kimura M, Horii T, Morita S, Soejima H, Kudo S, et al. Hum Mol Genet. 2008 Apr 15;17(8):1192–9. PubMed Europe PMC Scholia
- MeCP2, a key contributor to neurological disease, activates and represses transcription. Chahrour M, Jung SY, Shaw C, Zhou X, Wong STC, Qin J, et al. Science. 2008 May 30;320(5880):1224–9. PubMed Europe PMC Scholia
- MECP2 genomic structure and function: insights from ENCODE. Singh J, Saxena A, Christodoulou J, Ravine D. Nucleic Acids Res. 2008 Nov;36(19):6035–47. PubMed Europe PMC Scholia
- NNZ-2566: a Gly-Pro-Glu analogue with neuroprotective efficacy in a rat model of acute focal stroke. Bickerdike MJ, Thomas GB, Batchelor DC, Sirimanne ES, Leong W, Lin H, et al. J Neurol Sci. 2009 Mar 15;278(1–2):85–90. PubMed Europe PMC Scholia
- Ischemic preconditioning regulates expression of microRNAs and a predicted target, MeCP2, in mouse cortex. Lusardi TA, Farr CD, Faulkner CL, Pignataro G, Yang T, Lan J, et al. J Cereb Blood Flow Metab. 2010 Apr;30(4):744–56. PubMed Europe PMC Scholia
- Cross talk between microRNA and epigenetic regulation in adult neurogenesis. Szulwach KE, Li X, Smrt RD, Li Y, Luo Y, Lin L, et al. J Cell Biol. 2010 Apr 5;189(1):127–41. PubMed Europe PMC Scholia
- Rett syndrome microglia damage dendrites and synapses by the elevated release of glutamate. Maezawa I, Jin LW. J Neurosci. 2010 Apr 14;30(15):5346–56. PubMed Europe PMC Scholia
- Alternative polyadenylation of MeCP2: Influence of cis-acting elements and trans-acting factors. Newnham CM, Hall-Pogar T, Liang S, Wu J, Tian B, Hu J, et al. RNA Biol. 2010;7(3):361–72. PubMed Europe PMC Scholia
- Epigenetic regulation of miR-184 by MBD1 governs neural stem cell proliferation and differentiation. Liu C, Teng ZQ, Santistevan NJ, Szulwach KE, Guo W, Jin P, et al. Cell Stem Cell. 2010 May 7;6(5):433–44. PubMed Europe PMC Scholia
- A novel transcriptional regulator of myelin gene expression: implications for neurodevelopmental disorders. Vora P, Mina R, Namaka M, Frost EE. Neuroreport. 2010 Oct 6;21(14):917–21. PubMed Europe PMC Scholia
- Disrupted microRNA expression caused by Mecp2 loss in a mouse model of Rett syndrome. Urdinguio RG, Fernandez AF, Lopez-Nieva P, Rossi S, Huertas D, Kulis M, et al. Epigenetics. 2010 Oct 1;5(7):656–63. PubMed Europe PMC Scholia
- A brain-derived MeCP2 complex supports a role for MeCP2 in RNA processing. Long SW, Ooi JYY, Yau PM, Jones PL. Biosci Rep. 2011 Oct;31(5):333–43. PubMed Europe PMC Scholia
- Reduced AKT/mTOR signaling and protein synthesis dysregulation in a Rett syndrome animal model. Ricciardi S, Boggio EM, Grosso S, Lonetti G, Forlani G, Stefanelli G, et al. Hum Mol Genet. 2011 Mar 15;20(6):1182–96. PubMed Europe PMC Scholia
- Synaptic signaling and aberrant RNA splicing in autism spectrum disorders. Smith RM, Sadee W. Front Synaptic Neurosci. 2011 Jan 26;3:1. PubMed Europe PMC Scholia
- Chronic intermittent ethanol exposure and its removal induce a different miRNA expression pattern in primary cortical neuronal cultures. Guo Y, Chen Y, Carreon S, Qiang M. Alcohol Clin Exp Res. 2012 Jun;36(6):1058–66. PubMed Europe PMC Scholia
- Downregulation of CNPase in a MeCP2 deficient mouse model of Rett syndrome. Wu W, Gu W, Xu X, Shang S, Zhao Z. Neurol Res. 2012 Mar;34(2):107–13. PubMed Europe PMC Scholia
- Phosphorylation of distinct sites in MeCP2 modifies cofactor associations and the dynamics of transcriptional regulation. Gonzales ML, Adams S, Dunaway KW, LaSalle JM. Mol Cell Biol. 2012 Jul;32(14):2894–903. PubMed Europe PMC Scholia
- MeCP2 modulates gene expression pathways in astrocytes. Yasui DH, Xu H, Dunaway KW, Lasalle JM, Jin LW, Maezawa I. Mol Autism. 2013 Jan 25;4(1):3. PubMed Europe PMC Scholia
- Human-specific regulation of MeCP2 levels in fetal brains by microRNA miR-483-5p. Han K, Gennarino VA, Lee Y, Pang K, Hashimoto-Torii K, Choufani S, et al. Genes Dev. 2013 Mar 1;27(5):485–90. PubMed Europe PMC Scholia
- Dysregulation of the long non-coding RNA transcriptome in a Rett syndrome mouse model. Petazzi P, Sandoval J, Szczesna K, Jorge OC, Roa L, Sayols S, et al. RNA Biol. 2013 Jul;10(7):1197–203. PubMed Europe PMC Scholia
- Rett syndrome mutations abolish the interaction of MeCP2 with the NCoR/SMRT co-repressor. Lyst MJ, Ekiert R, Ebert DH, Merusi C, Nowak J, Selfridge J, et al. Nat Neurosci. 2013 Jul;16(7):898–902. PubMed Europe PMC Scholia
- MicroRNA-mediated epigenetic silencing of sirtuin1 contributes to impaired angiogenic responses. Volkmann I, Kumarswamy R, Pfaff N, Fiedler J, Dangwal S, Holzmann A, et al. Circ Res. 2013 Sep 27;113(8):997–1003. PubMed Europe PMC Scholia
- Identification of TET1 Partners That Control Its DNA-Demethylating Function. Cartron PF, Nadaradjane A, Lepape F, Lalier L, Gardie B, Vallette FM. Genes Cancer. 2013 May;4(5–6):235–41. PubMed Europe PMC Scholia
- Rett syndrome and MeCP2. Liyanage VRB, Rastegar M. Neuromolecular Med. 2014 Jun;16(2):231–64. PubMed Europe PMC Scholia
- Dysregulation of the IGF-I/PI3K/AKT/mTOR signaling pathway in autism spectrum disorders. Chen J, Alberts I, Li X. Int J Dev Neurosci. 2014 Jun;35:35–41. PubMed Europe PMC Scholia
- GluD1 is a common altered player in neuronal differentiation from both MECP2-mutated and CDKL5-mutated iPS cells. Livide G, Patriarchi T, Amenduni M, Amabile S, Yasui D, Calcagno E, et al. Eur J Hum Genet. 2015 Feb;23(2):195–201. PubMed Europe PMC Scholia
- Transcriptional regulation of GAD1 GABA synthesis gene in the prefrontal cortex of subjects with schizophrenia. Mitchell AC, Jiang Y, Peter C, Akbarian S. Schizophr Res. 2015 Sep;167(1–3):28–34. PubMed Europe PMC Scholia
- Misregulation of Alternative Splicing in a Mouse Model of Rett Syndrome. Li R, Dong Q, Yuan X, Zeng X, Gao Y, Chiao C, et al. PLoS Genet. 2016 Jun 28;12(6):e1006129. PubMed Europe PMC Scholia
- Population pharmacokinetics of NNZ-2566 in healthy subjects. Oosterholt SP, Horrigan J, Jones N, Glass L, Della Pasqua O. Eur J Pharm Sci. 2017 Nov 15;109S:S98–107. PubMed Europe PMC Scholia