Functions of histone modifications and histone modifiers in Schwann cells.


Journal

Glia
ISSN: 1098-1136
Titre abrégé: Glia
Pays: United States
ID NLM: 8806785

Informations de publication

Date de publication:
08 2020
Historique:
received: 14 10 2019
revised: 24 01 2020
accepted: 28 01 2020
pubmed: 9 2 2020
medline: 19 8 2021
entrez: 9 2 2020
Statut: ppublish

Résumé

Schwann cells (SCs) are the main glial cells present in the peripheral nervous system (PNS). Their primary functions are to insulate peripheral axons to protect them from the environment and to enable fast conduction of electric signals along big caliber axons by enwrapping them in a thick myelin sheath rich in lipids. In addition, SCs have the peculiar ability to foster axonal regrowth after a lesion by demyelinating and converting into repair cells that secrete neurotrophic factors and guide axons back to their former target to finally remyelinate regenerated axons. The different steps of SC development and their role in the maintenance of PNS integrity and regeneration after lesion are controlled by various factors among which transcription factors and chromatin-remodeling enzymes hold major functions. In this review, we discussed how histone modifications and histone-modifying enzymes control SC development, maintenance of PNS integrity and response to injury. The functions of histone modifiers as part of chromatin-remodeling complexes are discussed in another review published in the same issue of Glia.

Identifiants

pubmed: 32034929
doi: 10.1002/glia.23795
doi:

Substances chimiques

Histones 0

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

1584-1595

Subventions

Organisme : National Institutes of Health (NIH)
ID : 1R21CA235415-01A1
Pays : International

Informations de copyright

© 2020 The Authors. Glia published by Wiley Periodicals, Inc.

Références

Adilakshmi, T., Sudol, I., & Tapinos, N. (2012). Combinatorial action of miRNAs regulates transcriptional and post-transcriptional gene silencing following in vivo PNS injury. PLoS One, 7(7), e39674. https://doi.org/10.1371/journal.pone.0039674
Andrews, F. H., Strahl, B. D., & Kutateladze, T. G. (2016). Insights into newly discovered marks and readers of epigenetic information. Nature Chemical Biology, 12(9), 662-668. https://doi.org/10.1038/nchembio.2149
Arthur-Farraj, P. J., Latouche, M., Wilton, D. K., Quintes, S., Chabrol, E., Banerjee, A., … Jessen, K. R. (2012). c-Jun reprograms Schwann cells of injured nerves to generate a repair cell essential for regeneration. Neuron, 75(4), 633-647. https://doi.org/10.1016/j.neuron.2012.06.021
Arthur-Farraj, P. J., Morgan, C. C., Adamowicz, M., Gomez-Sanchez, J. A., Fazal, S. V., Beucher, A., … Aitman, T. J. (2017). Changes in the coding and non-coding transcriptome and DNA methylome that define the Schwann cell repair phenotype after nerve injury. Cell Reports, 20(11), 2719-2734. https://doi.org/10.1016/j.celrep.2017.08.064
Auerbach, R. (1954). Analysis of the developmental effects of a lethal mutation in the house mouse. Journal of Experimental Zoology, 127(2), 305-329. https://doi.org/10.1002/jez.1401270206
Bermingham, J. R., Jr., Scherer, S. S., O'Connell, S., Arroyo, E., Kalla, K. A., Powell, F. L., & Rosenfeld, M. G. (1996). Tst-1/Oct-6/SCIP regulates a unique step in peripheral myelination and is required for normal respiration. Genes & Development, 10(14), 1751-1762. https://doi.org/10.1101/gad.10.14.1751
Bremer, M., Frob, F., Kichko, T., Reeh, P., Tamm, E. R., Suter, U., & Wegner, M. (2011). Sox10 is required for Schwann-cell homeostasis and myelin maintenance in the adult peripheral nerve. Glia, 59(7), 1022-1032. https://doi.org/10.1002/glia.21173
Britsch, S., Goerich, D. E., Riethmacher, D., Peirano, R. I., Rossner, M., Nave, K. A., … Wegner, M. (2001). The transcription factor Sox10 is a key regulator of peripheral glial development. Genes & Development, 15(1), 66-78. https://doi.org/10.1101/gad.186601
Brügger, V., Duman, M., Bochud, M., Munger, E., Heller, M., Ruff, S., & Jacob, C. (2017). Delaying histone deacetylase response to injury accelerates conversion into repair Schwann cells and nerve regeneration. Nature Communications, 8, 14272. https://doi.org/10.1038/ncomms14272
Brügger, V., Engler, S., Pereira, J. A., Ruff, S., Horn, M., Welzl, H., … Jacob, C. (2015). HDAC1/2-dependent P0 expression maintains paranodal and nodal integrity independently of myelin stability through interactions with neurofascins. PLoS Biology, 13(9), e1002258. https://doi.org/10.1371/journal.pbio.1002258
Carrozza, M. J., Utley, R. T., Workman, J. L., & Côté, J. (2003). The diverse functions of histone acetyltransferase complexes. Trends in Genetics, 19(6), 321-329. https://doi.org/10.1016/s0168-9525(03)00115-x
Casadio, F., Lu, X., Pollock, S. B., LeRoy, G., Garcia, B. A., Muir, T. W., … Allis, C. D. (2013). H3R42me2a is a histone modification with positive transcriptional effects. Proceedings of the National Academy of Sciences of the United States of America, 110(37), 14894-14899. https://doi.org/10.1073/pnas.1312925110
Chen, Y., Wang, H., Yoon, S. O., Xu, X., Hottiger, M. O., Svaren, J., … Lu, Q. R. (2011). HDAC-mediated deacetylation of NF-kappaB is critical for Schwann cell myelination. Nature Neuroscience, 14(4), 437-441. https://doi.org/10.1038/nn.2780
Chen, Z. L., Yu, W. M., & Strickland, S. (2007). Peripheral regeneration. Annual Review of Neuroscience, 30, 209-233. https://doi.org/10.1146/annurev.neuro.30.051606.094337
Chittka, A., Arevalo, J. C., Rodriguez-Guzman, M., Perez, P., Chao, M. V., & Sendtner, M. (2004). The p75NTR-interacting protein SC1 inhibits cell cycle progression by transcriptional repression of cyclin E. The Journal of Cell Biology, 164(7), 985-996. https://doi.org/10.1083/jcb.200301106
de Ruijter, A. J., van Gennip, A. H., Caron, H. N., Kemp, S., & van Kuilenburg, A. B. (2003). Histone deacetylases (HDACs): Characterization of the classical HDAC family. The Biochemical Journal, 370(Pt 3), 737-749. https://doi.org/10.1042/BJ20021321
Decker, L., Desmarquet-Trin-Dinh, C., Taillebourg, E., Ghislain, J., Vallat, J. M., & Charnay, P. (2006). Peripheral myelin maintenance is a dynamic process requiring constant Krox20 expression. The Journal of Neuroscience, 26(38), 9771-9779. https://doi.org/10.1523/JNEUROSCI.0716-06.2006
Deckert, J., & Struhl, K. (2001). Histone acetylation at promoters is differentially affected by specific activators and repressors. Molecular and Cellular Biology, 21(8), 2726-2735. https://doi.org/10.1128/MCB.21.8.2726-2735.2001
Deng, Y., Wu, L. M. N., Bai, S., Zhao, C., Wang, H., Wang, J., … Lu, Q. R. (2017). A reciprocal regulatory loop between TAZ/YAP and G-protein Gαs regulates Schwann cell proliferation and myelination. Nature Communications, 8, 15161. https://doi.org/10.1038/ncomms15161
Dieker, J., & Muller, S. (2010). Epigenetic histone code and autoimmunity. Clinical Reviews in Allergy and Immunology, 39(1), 78-84. https://doi.org/10.1007/s12016-009-8173-7
Ernst, J., Kheradpour, P., Mikkelsen, T. S., Shoresh, N., Ward, L. D., Epstein, C. B., … Bernstein, B. E. (2011). Mapping and analysis of chromatin state dynamics in nine human cell types. Nature, 473(7345), 43-49. https://doi.org/10.1038/nature09906
Fernando, R. N., Cotter, L., Perrin-Tricaud, C., Berthelot, J., Bartolami, S., Pereira, J. A., … Tricaud, N. (2016). Optimal myelin elongation relies on YAP activation by axonal growth and inhibition by Crb3/Hippo pathway. Nature Communications, 7, 12186. https://doi.org/10.1038/ncomms12186
Finzsch, M., Schreiner, S., Kichko, T., Reeh, P., Tamm, E. R., Bosl, M. R., … Wegner, M. (2010). Sox10 is required for Schwann cell identity and progression beyond the immature Schwann cell stage. The Journal of Cell Biology, 189(4), 701-712. https://doi.org/10.1083/jcb.200912142
Franz, T. (1990). Defective ensheathment of motoric nerves in the splotch mutant mouse. Acta Anatomica (Basel), 138(3), 246-253. https://doi.org/10.1159/000146947
Frob, F., Bremer, M., Finzsch, M., Kichko, T., Reeh, P., Tamm, E. R., … Wegner, M. (2012). Establishment of myelinating Schwann cells and barrier integrity between central and peripheral nervous systems depend on Sox10. Glia, 60(5), 806-819. https://doi.org/10.1002/glia.22310
Fuhrmann, D., Mernberger, M., Nist, A., Stiewe, T., & Elsasser, H. P. (2018). Miz1 controls Schwann cell proliferation via H3K36(me2) demethylase Kdm8 to prevent peripheral nerve demyelination. The Journal of Neuroscience, 38(4), 858-877. https://doi.org/10.1523/JNEUROSCI.0843-17.2017
Ghislain, J., Desmarquet-Trin-Dinh, C., Jaegle, M., Meijer, D., Charnay, P., & Frain, M. (2002). Characterisation of cis-acting sequences reveals a biphasic, axon-dependent regulation of Krox20 during Schwann cell development. Development, 129(1), 155-166. Retrieved from. https://www.ncbi.nlm.nih.gov/pubmed/11782409
Gökbuget, D., Pereira, J. A., Bachofner, S., Marchais, A., Ciaudo, C., Stoffel, M., … Suter, U. (2015). The Lin28/let-7 axis is critical for myelination in the peripheral nervous system. Nature Communications, 6, 8584. https://doi.org/10.1038/ncomms9584
Gomez-Sanchez, J. A., Carty, L., Iruarrizaga-Lejarreta, M., Palomo-Irigoyen, M., Varela-Rey, M., Griffith, M., … Jessen, K. R. (2015). Schwann cell autophagy, myelinophagy, initiates myelin clearance from injured nerves. The Journal of Cell Biology, 210(1), 153-168. https://doi.org/10.1083/jcb.201503019
Gomez-Sanchez, J. A., Gomis-Coloma, C., Morenilla-Palao, C., Peiro, G., Serra, E., Serrano, M., & Cabedo, H. (2013). Epigenetic induction of the Ink4a/Arf locus prevents Schwann cell overproliferation during nerve regeneration and after tumorigenic challenge. Brain, 136(Pt 7), 2262-2278. https://doi.org/10.1093/brain/awt130
Gomis-Coloma, C., Velasco-Aviles, S., Gomez-Sanchez, J. A., Casillas-Bajo, A., Backs, J., & Cabedo, H. (2018). Class IIa histone deacetylases link cAMP signaling to the myelin transcriptional program of Schwann cells. The Journal of Cell Biology, 217(4), 1249-1268. https://doi.org/10.1083/jcb.201611150
Gordon, T., Chan, K. M., Sulaiman, O. A., Udina, E., Amirjani, N., & Brushart, T. M. (2009). Accelerating axon growth to overcome limitations in functional recovery after peripheral nerve injury. Neurosurgery, 65(4 Suppl), A132-A144. https://doi.org/10.1227/01.NEU.0000335650.09473.D3
Greer, C. B., Tanaka, Y., Kim, Y. J., Xie, P., Zhang, M. Q., Park, I. H., & Kim, T. H. (2015). Histone deacetylases positively regulate transcription through the elongation machinery. Cell Reports, 13(7), 1444-1455. https://doi.org/10.1016/j.celrep.2015.10.013
Grove, M., Kim, H., Santerre, M., Krupka, A. J., Han, S. B., Zhai, J., … Son, Y. J. (2017). YAP/TAZ initiate and maintain Schwann cell myelination. Elife, 6, e20982. https://doi.org/10.7554/eLife.20982
Hawkins, P. G., & Morris, K. V. (2008). RNA and transcriptional modulation of gene expression. Cell Cycle, 7(5), 602-607. Retrieved from. http://www.ncbi.nlm.nih.gov/pubmed/18256543
He, X., Zhang, L., Queme, L. F., Liu, X., Lu, A., Waclaw, R. R., … Lu, Q. R. (2018). A histone deacetylase 3-dependent pathway delimits peripheral myelin growth and functional regeneration. Nature Medicine, 24(3), 338-351. https://doi.org/10.1038/nm.4483
Heinen, A., Tzekova, N., Graffmann, N., Torres, K. J., Uhrberg, M., Hartung, H. P., & Kury, P. (2012). Histone methyltransferase enhancer of zeste homolog 2 regulates Schwann cell differentiation. Glia, 60(11), 1696-1708. https://doi.org/10.1002/glia.22388
Hodawadekar, S. C., & Marmorstein, R. (2007). Chemistry of acetyl transfer by histone modifying enzymes: Structure, mechanism and implications for effector design. Oncogene, 26(37), 5528-5540. https://doi.org/10.1038/sj.onc.1210619
Hung, H. A., Sun, G., Keles, S., & Svaren, J. (2015). Dynamic regulation of Schwann cell enhancers after peripheral nerve injury. The Journal of Biological Chemistry, 290(11), 6937-6950. https://doi.org/10.1074/jbc.M114.622878
Isaacman-Beck, J., Schneider, V., Franzini-Armstrong, C., & Granato, M. (2015). The lh3 glycosyltransferase directs target-selective peripheral nerve regeneration. Neuron, 88(4), 691-703. https://doi.org/10.1016/j.neuron.2015.10.004
Jacob, C. (2015). Transcriptional control of neural crest specification into peripheral glia. Glia, 63(11), 1883-1896. https://doi.org/10.1002/glia.22816
Jacob, C. (2017). Chromatin-remodeling enzymes in control of Schwann cell development, maintenance and plasticity. Current Opinion in Neurobiology, 47, 24-30. https://doi.org/10.1016/j.conb.2017.08.007
Jacob, C., Christen, C. N., Pereira, J. A., Somandin, C., Baggiolini, A., Lotscher, P., … Suter, U. (2011). HDAC1 and HDAC2 control the transcriptional program of myelination and the survival of Schwann cells. Nature Neuroscience, 14(4), 429-436. https://doi.org/10.1038/nn.2762
Jacob, C., Lebrun-Julien, F., & Suter, U. (2011). How histone deacetylases control myelination. Molecular Neurobiology, 44(3), 303-312. https://doi.org/10.1007/s12035-011-8198-9
Jacob, C., Lotscher, P., Engler, S., Baggiolini, A., Varum Tavares, S., Brugger, V., … Suter, U. (2014). HDAC1 and HDAC2 control the specification of neural crest cells into peripheral glia. The Journal of Neuroscience, 34(17), 6112-6122. https://doi.org/10.1523/JNEUROSCI.5212-13.2014
Jacques-Fricke, B. T., & Gammill, L. S. (2014). Neural crest specification and migration independently require NSD3-related lysine methyltransferase activity. Molecular Biology of the Cell, 25(25), 4174-4186. https://doi.org/10.1091/mbc.E13-12-0744
Jaegle, M., Mandemakers, W., Broos, L., Zwart, R., Karis, A., Visser, P., … Meijer, D. (1996). The POU factor Oct-6 and Schwann cell differentiation. Science, 273(5274), 507-510. https://doi.org/10.1126/science.273.5274.507
Jenuwein, T., & Allis, C. D. (2001). Translating the histone code. Science, 293(5532), 1074-1080. https://doi.org/10.1126/science.1063127
Jessen, K. R., & Arthur-Farraj, P. (2019). Repair Schwann cell update: Adaptive reprogramming, EMT, and stemness in regenerating nerves. Glia, 67(3), 421-437. https://doi.org/10.1002/glia.23532
Jessen, K. R., & Mirsky, R. (2005). The origin and development of glial cells in peripheral nerves. Nature Reviews. Neuroscience, 6(9), 671-682. https://doi.org/10.1038/nrn1746
Jessen, K. R., & Mirsky, R. (2008). Negative regulation of myelination: Relevance for development, injury, and demyelinating disease. Glia, 56(14), 1552-1565. https://doi.org/10.1002/glia.20761
Jessen, K. R., & Mirsky, R. (2016). The repair Schwann cell and its function in regenerating nerves. The Journal of Physiology, 594(13), 3521-3531. https://doi.org/10.1113/JP270874
Jessen, K. R., & Mirsky, R. (2019a). Schwann cell precursors; multipotent glial cells in embryonic nerves. Frontiers in Molecular Neuroscience, 12, 69. https://doi.org/10.3389/fnmol.2019.00069
Jessen, K. R., & Mirsky, R. (2019b). The success and failure of the Schwann cell response to nerve injury. Frontiers in Cellular Neuroscience, 13, 33. https://doi.org/10.3389/fncel.2019.00033
Jessen, K. R., Mirsky, R., & Lloyd, A. C. (2015). Schwann cells: Development and role in nerve repair. Cold Spring Harbor Perspectives in Biology, 7(7), a020487. https://doi.org/10.1101/cshperspect.a020487
Jopling, C., Boue, S., & Izpisua Belmonte, J. C. (2011). Dedifferentiation, transdifferentiation and reprogramming: Three routes to regeneration. Nature Reviews. Molecular Cell Biology, 12(2), 79-89. https://doi.org/10.1038/nrm3043
Kastriti, M. E., Kameneva, P., Kamenev, D., Dyachuk, V., Furlan, A., Hampl, M., … Adameyko, I. (2019). Schwann cell precursors generate the majority of chromaffin cells in Zuckerkandl organ and some sympathetic neurons in Paraganglia. Frontiers in Molecular Neuroscience, 12, 6. https://doi.org/10.3389/fnmol.2019.00006
Kim, D. H., Saetrom, P., Snove, O., Jr., & Rossi, J. J. (2008). MicroRNA-directed transcriptional gene silencing in mammalian cells. Proceedings of the National Academy of Sciences of the United States of America, 105(42), 16230-16235. https://doi.org/10.1073/pnas.0808830105
Klase, Z., Kale, P., Winograd, R., Gupta, M. V., Heydarian, M., Berro, R., … Kashanchi, F. (2007). HIV-1 TAR element is processed by Dicer to yield a viral micro-RNA involved in chromatin remodeling of the viral LTR. BMC Molecular Biology, 8, 63. https://doi.org/10.1186/1471-2199-8-63
Kuhlbrodt, K., Herbarth, B., Sock, E., Hermans-Borgmeyer, I., & Wegner, M. (1998). Sox10, a novel transcriptional modulator in glial cells. The Journal of Neuroscience, 18(1), 237-250. Retrieved from. https://www.ncbi.nlm.nih.gov/pubmed/9412504
Lange, U. C., Siebert, S., Wossidlo, M., Weiss, T., Ziegler-Birling, C., Walter, J., … Schneider, R. (2013). Dissecting the role of H3K64me3 in mouse pericentromeric heterochromatin. Nature Communications, 4, 2233. https://doi.org/10.1038/ncomms3233
Lee, W., Teckie, S., Wiesner, T., Ran, L., Prieto Granada, C. N., Lin, M., … Chi, P. (2014). PRC2 is recurrently inactivated through EED or SUZ12 loss in malignant peripheral nerve sheath tumors. Nature Genetics, 46(11), 1227-1232. https://doi.org/10.1038/ng.3095
Lin, H. P., Oksuz, I., Svaren, J., & Awatramani, R. (2018). Egr2-dependent microRNA-138 is dispensable for peripheral nerve myelination. Scientific Reports, 8(1), 3817. https://doi.org/10.1038/s41598-018-22010-8
Lippman, Z., May, B., Yordan, C., Singer, T., & Martienssen, R. (2003). Distinct mechanisms determine transposon inheritance and methylation via small interfering RNA and histone modification. PLoS Biology, 1(3), E67. https://doi.org/10.1371/journal.pbio.0000067
Liu, A., Li, J., Marin-Husstege, M., Kageyama, R., Fan, Y., Gelinas, C., & Casaccia-Bonnefil, P. (2006). A molecular insight of Hes5-dependent inhibition of myelin gene expression: Old partners and new players. The EMBO Journal, 25(20), 4833-4842. https://doi.org/10.1038/sj.emboj.7601352
Lopez-Anido, C., Poitelon, Y., Gopinath, C., Moran, J. J., Ma, K. H., Law, W. D., … Svaren, J. (2016). Tead1 regulates the expression of peripheral myelin protein 22 during Schwann cell development. Human Molecular Genetics, 25(14), 3055-3069. https://doi.org/10.1093/hmg/ddw158
Ma, K. H., Duong, P., Moran, J. J., Junaidi, N., & Svaren, J. (2018). Polycomb repression regulates Schwann cell proliferation and axon regeneration after nerve injury. Glia, 66(11), 2487-2502. https://doi.org/10.1002/glia.23500
Ma, K. H., Hung, H. A., Srinivasan, R., Xie, H., Orkin, S. H., & Svaren, J. (2015). Regulation of peripheral nerve myelin maintenance by gene repression through polycomb repressive complex 2. The Journal of Neuroscience, 35(22), 8640-8652. https://doi.org/10.1523/JNEUROSCI.2257-14.2015
Ma, K. H., Hung, H. A., & Svaren, J. (2016). Epigenomic regulation of Schwann cell reprogramming in peripheral nerve injury. The Journal of Neuroscience, 36(35), 9135-9147. https://doi.org/10.1523/JNEUROSCI.1370-16.2016
Maro, G. S., Vermeren, M., Voiculescu, O., Melton, L., Cohen, J., Charnay, P., & Topilko, P. (2004). Neural crest boundary cap cells constitute a source of neuronal and glial cells of the PNS. Nature Neuroscience, 7(9), 930-938. https://doi.org/10.1038/nn1299
Martinez-Moreno, M., O'Shea, T. M., Zepecki, J. P., Olaru, A., Ness, J. K., Langer, R., & Tapinos, N. (2017). Regulation of peripheral myelination through transcriptional buffering of Egr2 by an antisense long non-coding RNA. Cell Reports, 20(8), 1950-1963. https://doi.org/10.1016/j.celrep.2017.07.068
Matzke, M. A., Primig, M., Trnovsky, J., & Matzke, A. J. (1989). Reversible methylation and inactivation of marker genes in sequentially transformed tobacco plants. The EMBO Journal, 8(3), 643-649. Retrieved from. http://www.ncbi.nlm.nih.gov/pubmed/16453872
Mette, M. F., Aufsatz, W., van der Winden, J., Matzke, M. A., & Matzke, A. J. (2000). Transcriptional silencing and promoter methylation triggered by double-stranded RNA. The EMBO Journal, 19(19), 5194-5201. https://doi.org/10.1093/emboj/19.19.5194
Michan, S., & Sinclair, D. (2007). Sirtuins in mammals: Insights into their biological function. The Biochemical Journal, 404(1), 1-13. https://doi.org/10.1042/BJ20070140
Morris, K. V. (2009a). Long antisense non-coding RNAs function to direct epigenetic complexes that regulate transcription in human cells. Epigenetics, 4(5), 296-301. Retrieved from. http://www.ncbi.nlm.nih.gov/pubmed/19633414
Morris, K. V. (2009b). RNA-directed transcriptional gene silencing and activation in human cells. Oligonucleotides, 19(4), 299-306. https://doi.org/10.1089/oli.2009.0212
Morton, P. D., Dellarole, A., Theus, M. H., Walters, W. M., Berge, S. S., & Bethea, J. R. (2013). Activation of NF-kappaB in Schwann cells is dispensable for myelination in vivo. The Journal of Neuroscience, 33(24), 9932-9936. https://doi.org/10.1523/JNEUROSCI.2483-12.2013
Musselman, C. A., Lalonde, M. E., Côté, J., & Kutateladze, T. G. (2012). Perceiving the epigenetic landscape through histone readers. Nature Structural & Molecular Biology, 19(12), 1218-1227. https://doi.org/10.1038/nsmb.2436
Nave, K. A., & Schwab, M. H. (2005). Glial cells under remote control. Nature Neuroscience, 8(11), 1420-1422. https://doi.org/10.1038/nn1105-1420
Nave, K. A., & Trapp, B. D. (2008). Axon-glial signaling and the glial support of axon function. Annual Review of Neuroscience, 31, 535-561. https://doi.org/10.1146/annurev.neuro.30.051606.094309
Nave, K. A., & Werner, H. B. (2014). Myelination of the nervous system: Mechanisms and functions. Annual Review of Cell and Developmental Biology, 30, 503-533. https://doi.org/10.1146/annurev-cellbio-100913-013101
Ness, J. K., Skiles, A. A., Yap, E. H., Fajardo, E. J., Fiser, A., & Tapinos, N. (2016). Nuc-ErbB3 regulates H3K27me3 levels and HMT activity to establish epigenetic repression during peripheral myelination. Glia, 64(6), 977-992. https://doi.org/10.1002/glia.22977
Nocetti, N., & Whitehouse, I. (2016). Nucleosome repositioning underlies dynamic gene expression. Genes & Development, 30(6), 660-672. https://doi.org/10.1101/gad.274910.115
Olaopa, M., Zhou, H. M., Snider, P., Wang, J., Schwartz, R. J., Moon, A. M., & Conway, S. J. (2011). Pax3 is essential for normal cardiac neural crest morphogenesis but is not required during migration nor outflow tract septation. Developmental Biology, 356(2), 308-322. https://doi.org/10.1016/j.ydbio.2011.05.583
Omoto, S., & Fujii, Y. R. (2005). Regulation of human immunodeficiency virus 1 transcription by nef microRNA. The Journal of General Virology, 86(Pt 3), 751-755. https://doi.org/10.1099/vir.0.80449-0
Paratore, C., Goerich, D. E., Suter, U., Wegner, M., & Sommer, L. (2001). Survival and glial fate acquisition of neural crest cells are regulated by an interplay between the transcription factor Sox10 and extrinsic combinatorial signaling. Development, 128(20), 3949-3961. Retrieved from. https://www.ncbi.nlm.nih.gov/pubmed/11641219
Parkinson, D. B., Bhaskaran, A., Arthur-Farraj, P., Noon, L. A., Woodhoo, A., Lloyd, A. C., … Jessen, K. R. (2008). c-Jun is a negative regulator of myelination. The Journal of Cell Biology, 181(4), 625-637. https://doi.org/10.1083/jcb.200803013
Parrinello, S., Napoli, I., Ribeiro, S., Wingfield Digby, P., Fedorova, M., Parkinson, D. B., … Lloyd, A. C. (2010). EphB signaling directs peripheral nerve regeneration through Sox2-dependent Schwann cell sorting. Cell, 143(1), 145-155. https://doi.org/10.1016/j.cell.2010.08.039
Pattaroni, C., & Jacob, C. (2013). Histone methylation in the nervous system: Functions and dysfunctions. Molecular Neurobiology, 47(2), 740-756. https://doi.org/10.1007/s12035-012-8376-4
Pereira, J. A., Lebrun-Julien, F., & Suter, U. (2012). Molecular mechanisms regulating myelination in the peripheral nervous system. Trends in Neurosciences, 35(2), 123-134. https://doi.org/10.1016/j.tins.2011.11.006
Poitelon, Y., Lopez-Anido, C., Catignas, K., Berti, C., Palmisano, M., Williamson, C., … Feltri, M. L. (2016). YAP and TAZ control peripheral myelination and the expression of laminin receptors in Schwann cells. Nature Neuroscience, 19(7), 879-887. https://doi.org/10.1038/nn.4316
Rahman, S., Sowa, M. E., Ottinger, M., Smith, J. A., Shi, Y., Harper, J. W., & Howley, P. M. (2011). The Brd4 extraterminal domain confers transcription activation independent of pTEFb by recruiting multiple proteins, including NSD3. Molecular and Cellular Biology, 31(13), 2641-2652. https://doi.org/10.1128/MCB.01341-10
Roberts, S. L., Dun, X. P., Doddrell, R. D. S., Mindos, T., Drake, L. K., Onaitis, M. W., … Parkinson, D. B. (2017). Sox2 expression in Schwann cells inhibits myelination in vivo and induces influx of macrophages to the nerve. Development, 144(17), 3114-3125. https://doi.org/10.1242/dev.150656
Rohrich, M., Koelsche, C., Schrimpf, D., Capper, D., Sahm, F., Kratz, A., … Reuss, D. E. (2016). Methylation-based classification of benign and malignant peripheral nerve sheath tumors. Acta Neuropathologica, 131(6), 877-887. https://doi.org/10.1007/s00401-016-1540-6
Rosenberg, L. H., Cattin, A. L., Fontana, X., Harford-Wright, E., Burden, J. J., White, I. J., … Lloyd, A. C. (2018). HDAC3 regulates the transition to the homeostatic myelinating Schwann cell state. Cell Reports, 25(10), 2755-2765 e2755. https://doi.org/10.1016/j.celrep.2018.11.045
Ryu, E. J., Wang, J. Y., Le, N., Baloh, R. H., Gustin, J. A., Schmidt, R. E., & Milbrandt, J. (2007). Misexpression of Pou3f1 results in peripheral nerve hypomyelination and axonal loss. The Journal of Neuroscience, 27(43), 11552-11559. https://doi.org/10.1523/JNEUROSCI.5497-06.2007
Salzer, J. L. (2015). Schwann cell myelination. Cold Spring Harbor Perspectives in Biology, 7(8), a020529. https://doi.org/10.1101/cshperspect.a020529
Schwarz, D., Varum, S., Zemke, M., Schöler, A., Baggiolini, A., Draganova, K., … Sommer, L. (2014). Ezh2 is required for neural crest-derived cartilage and bone formation. Development, 141(4), 867-877. https://doi.org/10.1242/dev.094342
Schwenty-Lara, J., Nehl, D., & Borchers, A. (2019). The histone methyltransferase KMT2D, mutated in Kabuki syndrome patients, is required for neural crest cell formation and migration. Human Molecular Genetics. https://doi.org/10.1093/hmg/ddz284 [Epub ahead of print].
Sock, E., & Wegner, M. (2019). Transcriptional control of myelination and remyelination. Glia, 67(11), 2153-2165. https://doi.org/10.1002/glia.23636
Stassart, R. M., Fledrich, R., Velanac, V., Brinkmann, B. G., Schwab, M. H., Meijer, D., … Nave, K. A. (2013). A role for Schwann cell-derived neuregulin-1 in remyelination. Nature Neuroscience, 16(1), 48-54. https://doi.org/10.1038/nn.3281
Stierli, S., Imperatore, V., & Lloyd, A. C. (2019). Schwann cell plasticity-roles in tissue homeostasis, regeneration, and disease. Glia, 67(11), 2203-2215. https://doi.org/10.1002/glia.23643
Strahl, B. D., & Allis, C. D. (2000). The language of covalent histone modifications. Nature, 403(6765), 41-45. https://doi.org/10.1038/47412
Strobl-Mazzulla, P. H., Sauka-Spengler, T., & Bronner-Fraser, M. (2010). Histone demethylase JmjD2A regulates neural crest specification. Developmental Cell, 19(3), 460-468. https://doi.org/10.1016/j.devcel.2010.08.009
Svaren, J., & Meijer, D. (2008). The molecular machinery of myelin gene transcription in Schwann cells. Glia, 56(14), 1541-1551. https://doi.org/10.1002/glia.20767
Tan, Y., Zhang, B., Wu, T., Skogerbo, G., Zhu, X., Guo, X., … Chen, R. (2009). Transcriptional inhibiton of Hoxd4 expression by miRNA-10a in human breast cancer cells. BMC Molecular Biology, 10, 12. https://doi.org/10.1186/1471-2199-10-12
Topilko, P., Schneider-Maunoury, S., Levi, G., Baron-Van Evercooren, A., Chennoufi, A. B., Seitanidou, T., … Charnay, P. (1994). Krox-20 controls myelination in the peripheral nervous system. Nature, 371(6500), 796-799. https://doi.org/10.1038/371796a0
Torchia, J., Glass, C., & Rosenfeld, M. G. (1998). Co-activators and co-repressors in the integration of transcriptional responses. Current Opinion in Cell Biology, 10(3), 373-383. https://doi.org/10.1016/s0955-0674(98)80014-8
Tsai, E., & Casaccia, P. (2019). Mechano-modulation of nuclear events regulating oligodendrocyte progenitor gene expression. Glia, 67(7), 1229-1239. https://doi.org/10.1002/glia.23595
Vargas, M. E., & Barres, B. A. (2007). Why is Wallerian degeneration in the CNS so slow? Annual Review of Neuroscience, 30, 153-179. https://doi.org/10.1146/annurev.neuro.30.051606.094354
Veneti, Z., Gkouskou, K. K., & Eliopoulos, A. G. (2017). Polycomb repressor complex 2 in genomic instability and cancer. International Journal of Molecular Sciences, 18(8), E1657. https://doi.org/10.3390/ijms18081657
Viader, A., Chang, L. W., Fahrner, T., Nagarajan, R., & Milbrandt, J. (2011). MicroRNAs modulate Schwann cell response to nerve injury by reinforcing transcriptional silencing of dedifferentiation-related genes. The Journal of Neuroscience: The Official Journal of the Society for Neuroscience, 31(48), 17358-17369. https://doi.org/10.1523/JNEUROSCI.3931-11.2011
Walport, L. J., Hopkinson, R. J., Chowdhury, R., Schiller, R., Ge, W., Kawamura, A., & Schofield, C. J. (2016). Arginine demethylation is catalysed by a subset of JmjC histone lysine demethylases. Nature Communications, 7, 11974. https://doi.org/10.1038/ncomms11974
Wang, Z., Zang, C., Cui, K., Schones, D. E., Barski, A., Peng, W., & Zhao, K. (2009). Genome-wide mapping of HATs and HDACs reveals distinct functions in active and inactive genes. Cell, 138(5), 1019-1031. https://doi.org/10.1016/j.cell.2009.06.049
Wassenegger, M., Heimes, S., Riedel, L., & Sanger, H. L. (1994). RNA-directed de novo methylation of genomic sequences in plants. Cell, 76(3), 567-576. Retrieved from. http://www.ncbi.nlm.nih.gov/pubmed/8313476
Weider, M., & Wegner, M. (2017). SoxE factors: Transcriptional regulators of neural differentiation and nervous system development. Seminars in Cell & Developmental Biology, 63, 35-42. https://doi.org/10.1016/j.semcdb.2016.08.013
Woodhoo, A., Alonso, M. B., Droggiti, A., Turmaine, M., D'Antonio, M., Parkinson, D. B., … Jessen, K. R. (2009). Notch controls embryonic Schwann cell differentiation, postnatal myelination and adult plasticity. Nature Neuroscience, 12(7), 839-847. https://doi.org/10.1038/nn.2323
Woodhoo, A., & Sommer, L. (2008). Development of the Schwann cell lineage: From the neural crest to the myelinated nerve. Glia, 56(14), 1481-1490. https://doi.org/10.1002/glia.20723
Wu, L. M., Wang, J., Conidi, A., Zhao, C., Wang, H., Ford, Z., … Lu, Q. R. (2016). Zeb2 recruits HDAC-NuRD to inhibit notch and controls Schwann cell differentiation and remyelination. Nature Neuroscience, 19(8), 1060-1072. https://doi.org/10.1038/nn.4322
Zhang, J., Jing, L., Li, M., He, L., & Guo, Z. (2019). Regulation of histone arginine methylation/demethylation by methylase and demethylase (review). Molecular Medicine Reports, 19(5), 3963-3971. https://doi.org/10.3892/mmr.2019.10111
Zhao, S., Yue, Y., Li, Y., & Li, H. (2019). Identification and characterization of ‘readers’ for novel histone modifications. Current Opinion in Chemical Biology, 51, 57-65. https://doi.org/10.1016/j.cbpa.2019.04.001

Auteurs

Mert Duman (M)

Faculty of Biology, Institute of Developmental Biology and Neurobiology, Johannes Gutenberg University Mainz, Mainz, Germany.

Margot Martinez-Moreno (M)

Department of Neurosurgery, Molecular Neuroscience & Neuro-Oncology Laboratory, Brown University, Providence, Rhode Island.

Claire Jacob (C)

Faculty of Biology, Institute of Developmental Biology and Neurobiology, Johannes Gutenberg University Mainz, Mainz, Germany.

Nikos Tapinos (N)

Department of Neurosurgery, Molecular Neuroscience & Neuro-Oncology Laboratory, Brown University, Providence, Rhode Island.

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