Mecp2 and associated Rett syndrome (WP2910)

Mus musculus

Mecp2 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. The pathway is demonstrated for mouse but as the genes are highly conserved in mammals, many of these are valid for human, too.

Authors

Friederike Ehrhart , Egon Willighagen , Alex Pico , Kristina Hanspers , Elisa Cirillo , Lotte Sevenich , Martina Summer-Kutmon , and Eric Weitz

Activity

last edited

Discuss this pathway

Check for ongoing discussions or start your own.

Cited In

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

Mus musculus

Communities

ExRNA

Annotations

Pathway Ontology

regulatory pathway disease pathway regulatory pathway pertinent to the brain

Participants

Label Type Compact URI Comment
GABA Metabolite chebi:16865
Glutamate Metabolite chebi:29987
Ncor1 GeneProduct ensembl:ENSMUSG00000018501 nuclear receptor co-repressor 1
MYT1 GeneProduct ensembl:ENSMUSG00000010505 myelin transcription factor 1
proof of Mecp2 inhibition in Oligodendrocytes
Brn3 GeneProduct ensembl:ENSMUSG00000048349 POU domain, class 4, transcription factor 1
Apoc2 GeneProduct ensembl:ENSMUSG00000002992 apolipoprotein C-II
Fgf4 GeneProduct ensembl:ENSMUSG00000050917
Bdnf GeneProduct ensembl:ENSMUSG00000048482 brain derived neurotrophic factor
Nf1 GeneProduct ensembl:ENSMUSG00000020716 neurofibromatosis 1
Sst GeneProduct ensembl:ENSMUSG00000004366 Somatostatin
Nrep GeneProduct ensembl:ENSMUSG00000042834 neuronal regeneration related protein
Fut8 GeneProduct ensembl:ENSMUSG00000021065 fucosyltransferase 8
Mecp2 GeneProduct ensembl:ENSMUSG00000031393 methyl CpG binding protein 2
Brn2 GeneProduct ensembl:ENSMUSG00000095139 POU domain, class 3, transcription factor 2
YB1 GeneProduct ensembl:ENSMUSG00000028639 data obtained with human cell line and mouse primary tissue
Fgf3 GeneProduct ensembl:ENSMUSG00000031074 fibroblast growth factor 3
Smc3 GeneProduct ensembl:ENSMUSG00000024974 tructural maintenance of chromosomes 3
NR1/GRIN1 GeneProduct ensembl:ENSMUSG00000026959 related to FASD (fetal alcohole spectrum disorder)
NMDA receptor subunit: There are 8 different variants of NR1, produced by alternative splicing of GRIN1
Mef2c GeneProduct ensembl:ENSMUSG00000005583 myocyte enhancer factor 2C
TAP1 GeneProduct ensembl:ENSMUSG00000037321 transporter 1, ATP-binding cassette, sub-family B (MDR/TAP)
A2bp1 GeneProduct ensembl:ENSMUSG00000008658 ataxin 2 binding protein 1
CNPase GeneProduct ensembl:ENSMUSG00000006782 2',3'-cyclic nucleotide 3' phosphodiesterase
Ezh2 GeneProduct ensembl:ENSMUSG00000029687 histone H3 lysine 27 methyltransferase
Gamt GeneProduct ensembl:ENSMUSG00000020150 guanidinoacetate methyltransferase
Oprk1 GeneProduct ensembl:ENSMUSG00000025905 opioid receptor, kappa 1
Arhgef26 GeneProduct ensembl:ENSMUSG00000036885 Rho guanine nucleotide exchange factor (GEF) 26
Sin3a GeneProduct ensembl:ENSMUSG00000042557
SP1 GeneProduct ensembl:ENSMUSG00000001280 trans-acting transcription factor 1
GAD1 GeneProduct ensembl:ENSMUSG00000070880
TAF1 GeneProduct ensembl:ENSMUSG00000031314 TAF1 RNA polymerase II, TATA box binding protein (TBP)-associated factor
hnRNP H GeneProduct ensembl:ENSMUSG00000007850 HNRNPH1
Csrp1 GeneProduct ensembl:ENSMUSG00000026421 cysteine and glycine-rich protein 1
Dlx5 GeneProduct ensembl:ENSMUSG00000029755 distal-less homeobox 5
controls GABA production
Cdon GeneProduct ensembl:ENSMUSG00000038119 cell adhesion molecule-related/down-regulated by oncogenes
MYT1 GeneProduct ensembl:ENSMUSG00000010505 Myelin transcription factor 1
C/EBP GeneProduct ensembl:ENSMUSG00000071637 CCAAT/enhancer binding protein (Cebpd), delta
Mbp GeneProduct ensembl:ENSMUSG00000041607 myelin basic protein
BCL6 GeneProduct ensembl:ENSMUSG00000022508 B cell leukemia/lymphoma 6
Gabrr2 GeneProduct ensembl:ENSMUSG00000023267 gamma-aminobutyric acid (GABA) C receptor, subunit rho 2
CTCF GeneProduct ensembl:ENSMUSG00000005698 CCCTC-binding factor
SP3 GeneProduct ensembl:ENSMUSG00000027109 trans-acting transcription factor 3
PRPF3 GeneProduct ensembl:ENSMUSG00000015748 PRP3 pre-mRNA processing factor 3 homolog (yeast)
E2F1 GeneProduct ensembl:ENSMUSG00000027490 E2F transcription factor 1
REST GeneProduct ensembl:ENSMUSG00000029249 RE1-silencing transcription factor
Silences Mecp2 in non-neuronal tissue
Mag GeneProduct ensembl:ENSMUSG00000036634 myelin-associated glycoprotein
Fgf2 GeneProduct ensembl:ENSMUSG00000037225 fibroblast growth factor 2
Gprin1 GeneProduct ensembl:ENSMUSG00000069227 G protein-regulated inducer of neurite outgrowth 1
Tet1 GeneProduct ensembl:ENSMUSG00000047146 tet methylcytosine dioxygenase 1
hnRNP F GeneProduct ensembl:ENSMUSG00000042079 Hnrnpf
heterogeneous nuclear ribonucleoprotein F
YB1 GeneProduct ensembl:ENSMUSG00000028639 data obtained with human cell line and mouse primary tissue
Y box protein 1
Creb1 GeneProduct ensembl:ENSMUSG00000025958

References

  1. Neurotransmitters and their metabolites in the brains of fetal and newborn lambs. Richards GE, Gluckman PD, Mannelli SC. Life Sci. 1987 Oct 19;41(16):1881–4. PubMed Europe PMC Scholia
  2. 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
  3. 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
  4. 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
  5. 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
  6. 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
  7. 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
  8. 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
  9. 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
  10. 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
  11. 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
  12. 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
  13. 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
  14. 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
  15. 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
  16. 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
  17. 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
  18. 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
  19. 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
  20. 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
  21. 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
  22. 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
  23. 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
  24. 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
  25. Rett syndrome and MeCP2. Liyanage VRB, Rastegar M. Neuromolecular Med. 2014 Jun;16(2):231–64. PubMed Europe PMC Scholia
  26. 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