The transcriptional control of trunk neural crest induction, survival, and delamination

被引:319
作者
Cheung, M
Chaboissier, MC
Mynett, A
Hirst, E
Schedl, A
Briscoe, J
机构
[1] Natl Inst Med Res, London NW7 1AA, England
[2] Univ Nice, Inst Biochem, INSERM, U470, F-06108 Nice 2, France
基金
英国医学研究理事会;
关键词
D O I
10.1016/j.devcel.2004.12.010
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Trunk neural crest cells are generated at the border between the neural plate and nonneural ectoderm, where they initiate a distinct program of gene expression, undergo an epithelial-mesenchymal transition (EMT), and delaminate from the neuroepithelium. Here, we provide evidence that members of three families of transcription induce these properties in premigratory neural crest cells. Sox9 acts to provide the competence for neural crest cells to undergo an EMT and is required for trunk neural crest survival. In the absence of Sox9, cells apoptose prior to or shortly after delamination. Slug/Snail, in the presence of Sox9, is sufficient to induce an EMT in neural epithelial cells, while FoxD3 regulates the expression of cell-cell adhesion molecules required for neural crest migration. Together, the data suggest a model in which a combination of transcription factors regulates the acquisition of the diverse properties of neural crest cells.
引用
收藏
页码:179 / 192
页数:14
相关论文
共 50 条
[1]   EXPRESSION OF CELL-ADHESION MOLECULES DURING INITIATION AND CESSATION OF NEURAL CREST CELL-MIGRATION [J].
AKITAYA, T ;
BRONNERFRASER, M .
DEVELOPMENTAL DYNAMICS, 1992, 194 (01) :12-20
[2]   Essential role of Sox9 in the pathway that controls formation of cardiac valves and septa [J].
Akiyama, H ;
Chaboissier, MC ;
Behringer, RR ;
Rowitch, DH ;
Schedl, A ;
Epstein, JA ;
de Crombrugghe, B .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (17) :6502-6507
[3]  
AKLYAMA H, 2002, GENE DEV, V16, P2813
[4]   Pax3-expressing trigeminal placode cells can localize to trunk neural crest sites but are committed to a cutaneous sensory neuron fate [J].
Baker, CVH ;
Stark, MR ;
Bronner-Fraser, M .
DEVELOPMENTAL BIOLOGY, 2002, 249 (02) :219-236
[5]   The transcription factor Snail is a repressor of E-cadherin gene expression in epithelial tumour cells [J].
Batlle, E ;
Sancho, E ;
Franci, C ;
Domínguez, D ;
Monfar, M ;
Baulida, J ;
de Herreros, AG .
NATURE CELL BIOLOGY, 2000, 2 (02) :84-89
[6]   Haploinsufficiency of Sox9 results in defective cartilage primordia and premature skeletal mineralization [J].
Bi, WM ;
Huang, WD ;
Whitworth, DJ ;
Deng, JM ;
Zhang, ZP ;
Behringer, RR ;
de Crombrugghe, B .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (12) :6698-6703
[7]   Sox9 is required for cartilage formation [J].
Bi, WM ;
Deng, JM ;
Zhang, ZP ;
Behringer, RR ;
de Crombrugghe, B .
NATURE GENETICS, 1999, 22 (01) :85-89
[8]   The transcription factor Slug represses E-cadherin expression and induces epithelial to mesenchymal transitions:: a comparison with Snail and E47 repressors [J].
Bolós, V ;
Peinado, H ;
Pérez-Moreno, MA ;
Fraga, MF ;
Esteller, M ;
Cano, A .
JOURNAL OF CELL SCIENCE, 2003, 116 (03) :499-511
[9]   A homeodomain protein code specifies progenitor cell identity and neuronal fate in the ventral neural tube [J].
Briscoe, J ;
Pierani, A ;
Jessell, TM ;
Ericson, J .
CELL, 2000, 101 (04) :435-445
[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