Suppression of neural fate and control of inner ear morphogenesis by Tbx1

被引:134
作者
Raft, S
Nowotschin, S
Liao, J
Morrow, BE
机构
[1] Albert Einstein Coll Med, Dept Neurosci, Bronx, NY 10461 USA
[2] Albert Einstein Coll Med, Dept Mol Genet, Bronx, NY 10461 USA
来源
DEVELOPMENT | 2004年 / 131卷 / 08期
关键词
Tbx1; Ngn1; NeuroD; Bmp4; Otx1; otocyst; neurogenesis; patterning; mouse;
D O I
10.1242/dev.01067
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Inner ear sensory organs and VIIIth cranial ganglion neurons of the auditory/vestibular pathway derive from an ectodermal placode that invaginates to form an otocyst. We show that in the mouse otocyst epithelium, Tbx1 suppresses neurogenin I-mediated neural fate determination and is required for induction or proper patterning of gene expression related to sensory organ morphogenesis (Otx1 and Bmp4, respectively). Tbx1 loss-of-function causes dysregulation of neural competence in otocyst regions linked to the formation of either mechanosensory or structural sensory organ epithelia. Subsequently, VIIIth ganglion rudiment form is duplicated posteriorly, while the inner ear is hypoplastic and shows neither a vestibular apparatus nor a coiled cochlear duct. We propose that Tbx1 acts in the manner of a selector gene to control neural and sensory organ fate specification in the otocyst.
引用
收藏
页码:1801 / 1812
页数:12
相关论文
共 89 条
[1]   Epilepsy and brain abnormalities in mice lacking the Otx1 gene [J].
Acampora, D ;
Mazan, S ;
Avantaggiato, V ;
Barone, P ;
Tuorto, F ;
Lallemand, Y ;
Brulet, P ;
Simeone, A .
NATURE GENETICS, 1996, 14 (02) :218-222
[2]  
Adam J, 1998, DEVELOPMENT, V125, P4645
[3]  
ADKINS WY, 1974, ARCH OTOLARYNGOL, V100, P206
[4]   Mutations in human TBX3 alter limb, apocrine and genital development in ulnar-mammary syndrome [J].
Bamshad, M ;
Lin, RC ;
Law, DJ ;
Watkins, WS ;
Krakowiak, PA ;
Moore, ME ;
Franceschini, P ;
Lala, R ;
Holmes, LB ;
Gebuhr, TC ;
Bruneau, BG ;
Schinzel, A ;
Seidman, JG ;
Seidman, CE ;
Jorde, LB .
NATURE GENETICS, 1997, 16 (03) :311-315
[5]   Mutations in human cause limb and cardiac malformation in Holt-Oram syndrome [J].
Basson, CT ;
Bachinsky, DR ;
Lin, RC ;
Levi, T ;
Elkins, JA ;
Soults, J ;
Grayzel, D ;
Kroumpouzou, E ;
Traill, TA ;
LeblancStraceski, J ;
Renault, B ;
Kucherlapati, R ;
Seidman, JG ;
Seidman, CE .
NATURE GENETICS, 1997, 15 (01) :30-35
[6]   Math1:: An essential gene for the generation of inner ear hair cells [J].
Bermingham, NA ;
Hassan, BA ;
Price, SD ;
Vollrath, MA ;
Ben-Arie, N ;
Eatock, RA ;
Bellen, HJ ;
Lysakowski, A ;
Zoghbi, HY .
SCIENCE, 1999, 284 (5421) :1837-1841
[7]  
BLACK FO, 1975, ARCH OTOLARYNGOL, V101, P129
[8]   AN ANCIENT FAMILY OF EMBRYONICALLY EXPRESSED MOUSE GENES SHARING A CONSERVED PROTEIN MOTIF WITH THE T-LOCUS [J].
BOLLAG, RJ ;
SIEGFRIED, Z ;
CEBRATHOMAS, JA ;
GARVEY, N ;
DAVIDSON, EM ;
SILVER, LM .
NATURE GENETICS, 1994, 7 (03) :383-389
[9]   The T-box transcription factor gene TBX22 is mutated in X-linked cleft palate and ankyloglossia [J].
Braybrook, C ;
Doudney, K ;
Marçano, ACB ;
Arnason, A ;
Bjornsson, A ;
Patton, MA ;
Goodfellow, PJ ;
Moore, GE ;
Stanier, P .
NATURE GENETICS, 2001, 29 (02) :179-183
[10]   Molecular genetics of pattern formation in the inner ear: Do compartment boundaries play a role? [J].
Brigande, JV ;
Kiernan, AE ;
Gao, XY ;
Iten, LE ;
Fekete, DM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (22) :11700-11706