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The Transcription Factors Sox10 and Myrf Define an Essential Regulatory Network Module in Differentiating Oligodendrocytes
Open accessAbstract
Myelin is essential for rapid saltatory conduction and is produced by Schwann cells in the peripheral nervous system and oligodendrocytes in the central nervous system. In both cell types the transcription factor Sox10 is an essential component of the myelin-specific regulatory network. Here we identify Myrf as an oligodendrocyte-specific target of Sox10 and map a Sox10 responsive enhancer to an evolutionarily conserved element in intron 1 of the Myrf gene. Once induced, Myrf cooperates with Sox10 to implement the myelination program as evident from the physical interaction between both proteins and the synergistic activation of several myelin-specific genes. This is strongly reminiscent of the situation in Schwann cells where Sox10 first induces and then cooperates with Krox20 during myelination. Our analyses indicate that the regulatory network for myelination in oligodendrocytes is organized along similar general principles as the one in Schwann cells, but is differentially implemented.
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“This transition was accompanied by reduced activity of myelin-associated gene networks and diminished regulon activity of key transcriptional regulators, including MYRF and NKX6-2, which serve as central regulators of myelin gene expression programs (53-55) (Fig. 5J).”
From Molecular and cellular processes disrupted in the early postnatal Down syndrome prefrontal cortex (2026) · cites this paper as [54]
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Cites
Preparation of separate astroglial and oligodendroglial cell cultures from rat cerebral tissue.
McCarthy, K. D., & de Vellis, J. (1980) · The Journal of Cell Biology · doi:10.1083/jcb.85.3.890 · Cited by 3,825
Growth of a rat neuroblastoma cell line in serum-free supplemented medium.
Bottenstein, J. E., & SATO, G. H. (1979) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.76.1.514 · Cited by 2,268
Lu, Q. R., Sun, T., Zhu, Z., Ma, N., Garcia, M., Stiles, C. D., & Rowitch, D. H. (2002) · Cell · doi:10.1016/s0092-8674(02)00678-5 · Cited by 1,087
The bHLH Transcription Factors OLIG2 and OLIG1 Couple Neuronal and Glial Subtype Specification
Zhou, Q., & Anderson, D. J. (2002) · Cell · doi:10.1016/s0092-8674(02)00677-3 · Cited by 1,059
The transcription factor Sox10 is a key regulator of peripheral glial developmentPreprint
Britsch, S., Goerich, D. E., Riethmacher, D., Peirano, R. I., Rossner, M., Nave, K.-A., Birchmeier, C., & Wegner, M. (2001) · Genes & Development · doi:10.1101/gad.186601 · Cited by 941
Self-citationSox10, a Novel Transcriptional Modulator in Glial Cells
Kuhlbrodt, K., Herbarth, B., Sock, E., Hermans-Borgmeyer, I., & Wegner, M. (1998) · The Journal of Neuroscience · doi:10.1523/jneurosci.18-01-00237.1998 · Cited by 781
Self-citationStolt, C. C., Rehberg, S., Ader, M., Lommes, P., Riethmacher, D., Schachner, M., Bartsch, U., & Wegner, M. (2002) · Genes & Development · doi:10.1101/gad.215802 · Cited by 673
Self-citationThe Sox9 transcription factor determines glial fate choice in the developing spinal cord
Stolt, C. C., Lommes, P., Sock, E., Chaboissier, M.-C., Schedl, A., & Wegner, M. (2003) · Genes & Development · doi:10.1101/gad.259003 · Cited by 636
Self-citationMyelin gene regulatory factor is a critical transcriptional regulator required for CNS myelination
Emery, B., Agalliu, D., Cahoy, J. D., Watkins, T. A., Dugas, J. C., Mulinyawe, S. B., Ibrahim, A., Ligon, K. L., Rowitch, D. H., & Barres, B. A. (2009) · Cell · doi:10.1016/j.cell.2009.04.031 · Cited by 559
Control of oligodendrocyte differentiation by theNkx2.2homeodomain transcription factor
Qi, Y. B., Cai, J., Wu, Y., Wu, R., Lee, J. D., Fu, H. Q., Rao, M. S., Sussel, L., Rubenstein, J. L. R., & Qiu, M. S. (2001) · Development · doi:10.1242/dev.128.14.2723 · Cited by 351
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Regulation of prefrontal cortex myelination by the microbiota
Hoban, A. E., Stilling, R. M., Ryan, F. J., Shanahan, F., Dinan, T. G., Claesson, M. J., Clarke, G., & Cryan, J. F. (2016) · Translational Psychiatry · doi:10.1038/tp.2016.42 · Cited by 635
Rapid production of new oligodendrocytes is required in the earliest stages of motor-skill learning
Xiao, L., Ohayon, D., McKenzie, I. A., Sinclair-Wilson, A., Wright, J. L., Fudge, A. D., Emery, B., Li, H., & Richardson, W. D. (2016) · Nature Neuroscience · doi:10.1038/nn.4351 · Cited by 507
Emery, B., & Lu, Q. R. (2015) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a020461 · Cited by 307
Molecular Control of Oligodendrocyte Development
Elbaz, B., & Popko, B. (2019) · Trends in Neurosciences · doi:10.1016/j.tins.2019.01.002 · Cited by 304
Mechanisms regulating the development of oligodendrocytes and central nervous system myelin
Mitew, S., Hay, C. M., Peckham, H., Xiao, J., Koenning, M., & Emery, B. (2013) · Neuroscience · doi:10.1016/j.neuroscience.2013.11.029 · Cited by 268
Microglia: Housekeeper of the Central Nervous System
Kabba, J. A., Xu, Y., Christian, H., Ruan, W., Kitchen, C., Xiang, Y., Zhang, L., Saavedra, J. M., & Pang, T. (2017) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-017-0504-2 · Cited by 265
Oligodendrocyte lineage cells and depression
Zhou, B., Zhu, Z., Ransom, B. R., & Tong, X. (2020) · Molecular Psychiatry · doi:10.1038/s41380-020-00930-0 · Cited by 245
Spaas, J., van Veggel, L., Schepers, M., Tiane, A., van Horssen, J., Wilson, D. M., Moya, P. R., Piccart, E., Hellings, N., Eijnde, B. O., et al. (2021) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-021-03802-0 · Cited by 224
Huang, B., Wei, W., Wang, G., Gaertig, M. A., Feng, Y., Wang, W., Li, X., & Li, S. (2015) · Neuron · doi:10.1016/j.neuron.2015.02.026 · Cited by 179
CNS myelination and remyelination depend on fatty acid synthesis by oligodendrocytes
Dimas, P., Montani, L., Pereira, J. A., Moreno, D., Trötzmüller, M., Gerber, J., Semenkovich, C. F., Köfeler, H. C., & Suter, U. (2019) · eLife · doi:10.7554/elife.44702 · Cited by 178
Gain of Olig2 function in oligodendrocyte progenitors promotes remyelination
Wegener, A., Deboux, C., Bachelin, C., Frah, M., Kerninon, C., Seilhean, D., Weider, M., Wegner, M., & Nait‐Oumesmar, B. (2014) · Brain · doi:10.1093/brain/awu375 · Cited by 180
Self-citationYang, H., Vainshtein, A., Maik-Rachline, G., & Peles, E. (2016) · Nature Communications · doi:10.1038/ncomms10884 · Cited by 150
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Lyons, D. A., & Talbot, W. S. (2014) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a020586 · Cited by 163
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Keogh, C. E., Kim, D. H. J., Pusceddu, M. M., Knotts, T. A., Rabasa, G., Sladek, J. A., Hsieh, M. T., Honeycutt, M., Brust-Mascher, I., Barboza, M., et al. (2021) · Brain, Behavior, and Immunity · doi:10.1016/j.bbi.2020.11.001 · Cited by 137
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Dravis, C., Spike, B. T., Harrell, J. C., Johns, C., Trejo, C. L., Southard‐Smith, E. M., Perou, C. M., & Wahl, G. M. (2015) · Cell Reports · doi:10.1016/j.celrep.2015.08.040 · Cited by 131
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Tiane, A., Schepers, M., Rombaut, B., Hupperts, R., Prickaerts, J., Hellings, N., van den Hove, D., & Vanmierlo, T. (2019) · Cells · doi:10.3390/cells8101236 · Cited by 128
Qi, H., Yu, L., Zhou, X., Wynn, J., Zhao, H., Guo, Y., Zhu, N., Kitaygorodsky, A., Hernan, R., Aspelund, G., et al. (2018) · PLoS Genetics · doi:10.1371/journal.pgen.1007822 · Cited by 122
Myelin regulatory factor drives remyelination in multiple sclerosis
Duncan, G. J., Plemel, J. R., Assinck, P., Manesh, S. B., Muir, F. G. W., Hirata, R., Berson, M., Liu, J., Wegner, M., Emery, B., et al. (2017) · Acta Neuropathologica · doi:10.1007/s00401-017-1741-7 · Cited by 120
Self-citationStem cell factor Sox2 and its close relative Sox3 have differentiation functions in oligodendrocytes
Hoffmann, S., Hos, D., Küspert, M., Lang, R. A., Lovell-Badge, R. H., Wegner, M., & Reiprich, S. (2013) · Development · doi:10.1242/dev.098418 · Cited by 115
Self-citationForbes, T. A., Goldstein, E. Z., Dupree, J. L., Jablonska, B., Scafidi, J., Adams, K. L., Kawasawa, Y. I., Hashimoto‐Torii, K., & Gallo, V. (2020) · Nature Communications · doi:10.1038/s41467-020-14762-7 · Cited by 108
SoxE factors: Transcriptional regulators of neural differentiation and nervous system development
Weider, M., & Wegner, M. (2016) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2016.08.013 · Cited by 115
Self-citationOligodendroglia Are Particularly Vulnerable to Oxidative Damage after Neurotrauma In Vivo
Giacci, M. K., Bartlett, C. A., Smith, N. M., Iyer, K. S., Toomey, L. M., Jiang, H., Guagliardo, P. R., Kilburn, M. R., & Fitzgerald, M. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.1898-17.2018 · Cited by 113
All Wrapped Up: Environmental Effects on Myelination
Forbes, T. A., & Gallo, V. (2017) · Trends in Neurosciences · doi:10.1016/j.tins.2017.06.009 · Cited by 114
Transcriptional control of myelination and remyelination
Sock, E., & Wegner, M. (2019) · Glia · doi:10.1002/glia.23636 · Cited by 109
Self-citationThe white matter is a pro-differentiative niche for glioblastoma
Brooks, L. J., Clements, M., Burden, J. J., Kocher, D., Richards, L., Devesa, S. C., Zakka, L., Woodberry, M., Ellis, M. J., Jaunmuktane, Z., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-22225-w · Cited by 106
Differential Sox10 genomic occupancy in myelinating glia
Lopez‐Anido, C., Sun, G., Koenning, M., Srinivasan, R., Hung, H. A., Emery, B., Keleş, S., & Svaren, J. P. (2015) · Glia · doi:10.1002/glia.22855 · Cited by 103
Sock, E., & Wegner, M. (2021) · Developmental Neurobiology · doi:10.1002/dneu.22849 · Cited by 105
Self-citationYAP/TAZ initiate and maintain Schwann cell myelination
Grove, M., Kim, H., Santerre, M., Krupka, A. J., Han, S. B., Zhai, J., Cho, J. Y., Park, R., Harris, M. Y., Kim, S., et al. (2017) · eLife · doi:10.7554/elife.20982 · Cited by 101
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Developmentally regulated signaling pathways in glioma invasion
Mehta, S. V., & Cascio, C. L. (2017) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-017-2608-8 · Cited by 93
Weider, M., Starost, L. J., Groll, K., Küspert, M., Sock, E., Wedel, M., Fröb, F., Schmitt, C., Baroti, T., Hartwig, A. C., et al. (2018) · Nature Communications · doi:10.1038/s41467-018-03336-3 · Cited by 92
Self-citationSox8 and Sox10 jointly maintain myelin gene expression in oligodendrocytes
Turnescu, T., Arter, J., Reiprich, S., Tamm, E. R., Waisman, A., & Wegner, M. (2017) · Glia · doi:10.1002/glia.23242 · Cited by 79
Self-citationDevelopment of myelinating glia: An overview
Cristobal, C. D., & Lee, H. K. (2022) · Glia · doi:10.1002/glia.24238 · Cited by 85
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Reiprich, S., & Wegner, M. (2014) · Cell and Tissue Research · doi:10.1007/s00441-014-1909-6 · Cited by 76
Self-citationGarnai, S. J., Brinkmeier, M. L., Emery, B., Alemán, T. S., Pyle, L. C., Veleva-Rotse, B. O., Sisk, R. A., Rozsa, F. W., Ozel, A. B., Li, J. Z., et al. (2019) · PLoS Genetics · doi:10.1371/journal.pgen.1008130 · Cited by 76
Malaiya, S., Cortes-Gutierrez, M., Herb, B. R., Coffey, S. R., Legg, S. R. W., Cantle, J. P., Colantuoni, C., Carroll, J. B., & Ament, S. A. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.2074-20.2021 · Cited by 71
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Li, N., & Leung, G. (2015) · BioMed Research International · doi:10.1155/2015/235195 · Cited by 76
Epigenetic activation of a RAS/MYC axis in H3.3K27M-driven cancer
Pajovic, S., Siddaway, R., Bridge, T., Sheth, J., Rakopoulos, P., Kim, B., Ryall, S. T., Agnihotri, S., Phillips, L., Yu, M., et al. (2020) · Nature Communications · doi:10.1038/s41467-020-19972-7 · Cited by 70
Quan, L., Uyeda, A., & Muramatsu, R. (2022) · Inflammation and Regeneration · doi:10.1186/s41232-022-00193-y · Cited by 75
Wedel, M., Fröb, F., Elsesser, O., Wittmann, M., Lie, D. C., Reis, A., & Wegner, M. (2020) · Nucleic Acids Research · doi:10.1093/nar/gkaa218 · Cited by 68
Self-citationChen, C. Z.-Y., Neumann, B., Förster, S., & Franklin, R. J. M. (2021) · Open Biology · doi:10.1098/rsob.200352 · Cited by 66
Review of the phenotypic spectrum associated with haploinsufficiency of MYRF
Rossetti, L. Z., Glinton, K. E., Yuan, B., Liu, P., Pillai, N. R., Mizerik, E. A., Magoulas, P. L., Rosenfeld, J. A., Karaviti, L. P., Sutton, V. R., et al. (2019) · American Journal of Medical Genetics Part A · doi:10.1002/ajmg.a.61182 · Cited by 66
Khanghahi, A. M., Satarian, L., Deng, W., Baharvand, H., & Javan, M. (2018) · PLoS ONE · doi:10.1371/journal.pone.0203785 · Cited by 68
Transcription factor Sox10 regulates oligodendroglial Sox9 levels via microRNAs
Reiprich, S., Cantone, M., Weider, M., Baroti, T., Wittstatt, J., Schmitt, C., Küspert, M., Vera, J., & Wegner, M. (2017) · Glia · doi:10.1002/glia.23146 · Cited by 65
Self-citationBischof, M., Weider, M., Küspert, M., Nave, K., & Wegner, M. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.1468-14.2015 · Cited by 63
Self-citationPost-translational Modifications of OLIG2 Regulate Glioma Invasion through the TGF-β Pathway
Singh, S. K., Fiorelli, R., Kupp, R., Rajan, S., Szeto, E., Cascio, C. L., Maire, C. L., Sun, Y., Alberta, J. A., Eschbacher, J. M., et al. (2016) · Cell Reports · doi:10.1016/j.celrep.2016.06.045 · Cited by 60
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Curry, R. N., & Glasgow, S. M. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.659055 · Cited by 61
Myrf guides target gene selection of transcription factor Sox10 during oligodendroglial development
Aprato, J., Sock, E., Weider, M., Elsesser, O., Fröb, F., & Wegner, M. (2019) · Nucleic Acids Research · doi:10.1093/nar/gkz1158 · Cited by 59
Self-citationZhang, M., Wang, J., Zhang, K., Lu, G., Liu, Y., Ren, K., Wang, W., Xin, D. E., Xu, L., Mao, H., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-25353-5 · Cited by 61
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Duman, M., Vaquie, A. M., Nocera, G., Heller, M., Stumpe, M., Sankar, D. S., Dengjel, J., Meijer, D., Yamaguchi, T., Matthias, P., et al. (2020) · Nature Communications · doi:10.1038/s41467-020-17243-z · Cited by 56
The Initial Myelination in the Central Nervous System
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Cantone, M., Küspert, M., Reiprich, S., Lai, X., Eberhardt, M., Göttle, P., Beyer, F., Azim, K., Küry, P., Wegner, M., et al. (2019) · Glia · doi:10.1002/glia.23569 · Cited by 59
Self-citationWeider, M., Wegener, A., Schmitt, C., Küspert, M., Hillgärtner, S., Bösl, M., Hermans-Borgmeyer, I., Nait-Oumesmar, B., & Wegner, M. (2015) · PLoS Genetics · doi:10.1371/journal.pgen.1005008 · Cited by 51
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Zhao, X., & Jacob, C. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24076373 · Cited by 46
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Corradini, B. R., Iamashita, P., Tampellini, E., Farfel, J. M., Grinberg, L. T., & Moreira‐Filho, C. A. (2014) · BioMed Research International · doi:10.1155/2014/543673 · Cited by 41
Matsumoto, S., Banine, F., Feistel, K., Foster, S. C., Xing, R., Struve, J., & Sherman, L. (2016) · Developmental Biology · doi:10.1016/j.ydbio.2016.04.003 · Cited by 40
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Elsesser, O., Fröb, F., Küspert, M., Tamm, E. R., Fujii, T., Fukunaga, R., & Wegner, M. (2019) · Nucleic Acids Research · doi:10.1093/nar/gkz376 · Cited by 42
Self-citationWarnock, A., Toomey, L. M., Wright, A. J., Fisher, K., Won, Y., Anyaegbu, C. C., & Fitzgerald, M. (2020) · Journal of Neurotrauma · doi:10.1089/neu.2019.6890 · Cited by 36
Cheng, G. W.-Y., Mok, K. K.-S., Yeung, S. H.-S., Kofler, J., Herrup, K., & Tse, K.-H. (2022) · Journal of Neuropathology & Experimental Neurology · doi:10.1093/jnen/nlac054 · Cited by 36
Tomàs-Roig, J., Wirths, O., Salinas, G., & Havemann‐Reinecke, U. (2016) · CNS Neuroscience & Therapeutics · doi:10.1111/cns.12506 · Cited by 35
Oligodendrocytes and myelin: Active players in neurodegenerative brains?
Chen, J., Wang, F., Huang, N., Xiao, L., & Mei, F. (2022) · Developmental Neurobiology · doi:10.1002/dneu.22867 · Cited by 37
Bernhardt, C., Sock, E., Fröb, F., Hillgärtner, S., Nemer, M. J., & Wegner, M. (2022) · Nucleic Acids Research · doi:10.1093/nar/gkac953 · Cited by 34
Self-citationRegulators of Oligodendrocyte DifferentiationPreprint
Emery, B., & Wood, T. L. (2024) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a041358 · Cited by 36
Ulanska-Poutanen, J., Mieczkowski, J., Zhao, C., Konarzewska, K., Kaza, B., Pohl, H., Bugajski, Ł., Kaminska, B., Franklin, R. J. M., & Zawadzka, M. (2018) · eLife · doi:10.7554/elife.30325 · Cited by 32
Samudyata, S., Castelo‐Branco, G., & Liu, J. (2020) · Glia · doi:10.1002/glia.23820 · Cited by 34
Cross, S. H., McKie, L., Hurd, T. W., Riley, S., Wills, J. C., Barnard, A. R., Young, F., MacLaren, R. E., & Jackson, I. J. (2020) · PLoS Genetics · doi:10.1371/journal.pgen.1008583 · Cited by 31
Muth, K. N., Piefke, S., Weider, M., Sock, E., Hermans‐Borgmeyer, I., Wegner, M., & Küspert, M. (2016) · Glia · doi:10.1002/glia.23044 · Cited by 32
Self-citationGhosh, T., Almeida, R., Zhao, C., Mannioui, A., Martin, E., Fleet, A., Chen, C. Z.-Y., Assinck, P., Ellams, S., González, G. A., et al. (2024) · Cell · doi:10.1016/j.cell.2024.01.011 · Cited by 39
Yang, F., Guan, Y., Feng, X. M., Rolfs, A., Schlüter, H., & Luo, J. (2019) · Molecular Brain · doi:10.1186/s13041-019-0440-9 · Cited by 32
Novel truncation mutations in MYRF cause autosomal dominant high hyperopia mapped to 11p12–q13.3
Xiao, X., Sun, W., Ouyang, J., Li, S., Jia, X., Tan, Z., Hejtmancik, J. F., & Zhang, Q. (2019) · Human Genetics · doi:10.1007/s00439-019-02039-z · Cited by 30
The RNA binding protein fragile X mental retardation protein promotes myelin sheath growth
Doll, C. A., Yergert, K. M., & Appel, B. (2019) · Glia · doi:10.1002/glia.23731 · Cited by 27
Mertelmeyer, S., Weider, M., Baroti, T., Reiprich, S., Fröb, F., Stolt, C. C., Wagner, K., & Wegner, M. (2020) · Scientific Reports · doi:10.1038/s41598-020-74664-y · Cited by 26
Self-citationFröb, F., Sock, E., Tamm, E. R., Saur, A., Hillgärtner, S., Williams, T., Fujii, T., Fukunaga, R., & Wegner, M. (2019) · Nature Communications · doi:10.1038/s41467-019-10287-w · Cited by 29
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Metadata
- Authors
- Hornig, J., Fröb, F., Vogl, M. R., Hermans-Borgmeyer, I., Tamm, E. R., & Wegner, M.
- Affiliations
- Friedrich-Alexander-Universität Erlangen-Nürnberg (DE)
- University of Regensburg (DE)
- Corresponding author
- Wegner, Michael
- Venue
- PLoS Genetics
- Publisher
- Public Library of Science (PLoS)
- Published
- 2013-10-31
- Volume
- 9
- Issue
- 10
- Pages
- e1003907
- ISSN
- 1553-7390 (ISSN-L)
- 1553-7404
- PMC
- PMC3814293
- OpenAlex
- W2083561210
- Cited by
- 228
- References
- 47
- Citations by year
- 2026: 15 · 2025: 22 · 2024: 19 · 2023: 11 · 2022: 24 · 2021: 19 · 2020: 23 · 2019: 24 · 2018: 16 · 2017: 16 · 2016: 17 · 2015: 14 · 2014: 5 · 2013: 3
- FWCI
- 4.83
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Locations
- PLoS Genetics (publishedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Figshare (submittedVersion, cc-by)
- OPUS FAU (Kooperativer Bibliotheksverbund Berlin-Brandenburg (KOBV), on behalf of the Universitätsbibliothek Erlangen-Nürnberg) (submittedVersion)
- Funders
- Deutsche Forschungsgemeinschaft (We1326/11)
- Topics
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Chromatin Dynamics
- Keywords
- SOX10, MYRF, oligodendrocyte differentiation, myelination, transcriptional regulatory networks, enhancers, Krox20, Schwann cells, protein-protein interaction, central nervous system myelin
- MeSH terms
- Animals, Cell Differentiation, Cell Line, Central Nervous System, High Mobility Group Proteins, Humans, Mice, Transgenic, Myelin Sheath, Oligodendroglia, Schwann Cells, Transcription Factors, Gene Expression Regulation, Developmental, Mice, Early Growth Response Protein 2, Gene Regulatory Networks, SOXE Transcription Factors
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