The Molecular Machinery of Myelin Gene Transcription in Schwann Cells

被引:188
作者
Svaren, John [2 ,3 ]
Meijer, Dies [1 ]
机构
[1] ErasmusMC, Dept Cell Biol & Genet, NL-3000 AC Rotterdam, Netherlands
[2] Univ Wisconsin, Sch Vet Med, Dept Comparat Biosci, Madison, WI 53706 USA
[3] Univ Wisconsin, Waisman Ctr, Madison, WI 53706 USA
基金
美国国家卫生研究院;
关键词
CMT; peripheral neuropathy; gene regulation; Pou3f1; Egr2; Sox10; Srebp;
D O I
10.1002/glia.20767
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
During late fetal life, Schwann cells in the peripheral nerves singled out by the larger axons will transit through a promyelinating stage before exiting the cell cycle and initiating myelin formation. A network of extra- and intracellular signaling pathways, regulating a transcriptional program of cell differentiation, governs this progression of cellular changes, culminating in a highly differentiated cell. In this review. we focus on the roles of a number of transcription factors not only in myelination, during normal development, but also in demyelination, following nerve trauma. These factors include specification factors involved in early development of Schwann cells from neural crest (SOX10) as well as factors specifically required for transitions into the promyelinating and myelinating stages (Oct6/Scip and Krox20/Egr2). From this description, we can glean the first, Still very incomplete, contours of a gene regulatory network that governs myelination and demyelination during development and regeneration. (C)2008 Wiley-Liss, Inc.
引用
收藏
页码:1541 / 1551
页数:11
相关论文
共 115 条
[1]   A double point mutation in the DNA-binding region of Egr2 switches its function from inhibition to induction of proliferation: A potential contribution to the development of congenital hypomyelinating neuropathy [J].
Arthur-Farraj, Peter ;
Mirsky, Rhona ;
Parkinson, David B. ;
Jessen, Kristjan R. .
NEUROBIOLOGY OF DISEASE, 2006, 24 (01) :159-169
[2]   The POU protein Oct-6 is a nucleocytoplasmic shuttling protein [J].
Baranek, C ;
Sock, E ;
Wegner, M .
NUCLEIC ACIDS RESEARCH, 2005, 33 (19) :6277-6286
[3]  
Bellone E, 1999, Hum Mutat, V14, P353, DOI 10.1002/(SICI)1098-1004(199910)14:4<353::AID-HUMU17>3.0.CO
[4]  
2-4
[5]   The claw paw mutation reveals a role for Lgi4 in peripheral nerve development [J].
Bermingham, JR ;
Shearin, H ;
Pennington, J ;
O'Moore, J ;
Jaegle, M ;
Driegen, S ;
van Zon, A ;
Darbas, A ;
Özkaynak, E ;
Ryu, EJ ;
Milbrandt, J ;
Meijer, D .
NATURE NEUROSCIENCE, 2006, 9 (01) :76-84
[6]  
Bermingham JR, 2002, J NEUROSCI, V22, P10217
[7]   Tst-1/Oct-6/SCIP regulates a unique step in peripheral myelination and is required for normal respiration [J].
Bermingham, JR ;
Scherer, SS ;
OConnell, S ;
Arroyo, E ;
Kalla, KA ;
Powell, FL ;
Rosenfeld, MG .
GENES & DEVELOPMENT, 1996, 10 (14) :1751-1762
[8]   Human Connexin 32, a gap junction protein altered in the X-linked form of Charcot-Marie-Tooth disease, is directly regulated by the transcription factor SOX10 [J].
Bondurand, N ;
Girard, M ;
Pingault, V ;
Lemort, N ;
Dubourg, O ;
Goossens, M .
HUMAN MOLECULAR GENETICS, 2001, 10 (24) :2783-2795
[9]   Mi-2/NuRD: multiple complexes for many purposes [J].
Bowen, NJ ;
Fujita, N ;
Kajita, M ;
Wade, PA .
BIOCHIMICA ET BIOPHYSICA ACTA-GENE STRUCTURE AND EXPRESSION, 2004, 1677 (1-3) :52-57
[10]   The transcription factor Sox10 is a key regulator of peripheral glial development [J].
Britsch, S ;
Goerich, DE ;
Riethmacher, D ;
Peirano, RI ;
Rossner, M ;
Nave, KA ;
Birchmeier, C ;
Wegner, M .
GENES & DEVELOPMENT, 2001, 15 (01) :66-78