Control of segment number in vertebrate embryos

被引:328
作者
Gomez, Celine [1 ]
Ozbudak, Ertugrul M. [1 ]
Wunderlich, Joshua [1 ]
Baumann, Diana [1 ]
Lewis, Julian [2 ]
Pourquie, Olivier [1 ,3 ]
机构
[1] Stowers Inst Med Res, Kansas City, MO 64110 USA
[2] London Res Inst, Canc Res UK, Vertebrate Dev Lab, London WC2A 3PX, England
[3] Howard Hughes Med Inst, Kansas City, MO 64110 USA
关键词
D O I
10.1038/nature07020
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The vertebrate body axis is subdivided into repeated segments, best exemplified by the vertebrae that derive from embryonic somites. The number of somites is precisely defined for any given species but varies widely from one species to another. To determine the mechanism controlling somite number, we have compared somitogenesis in zebrafish, chicken, mouse and corn snake embryos. Here we present evidence that in all of these species a similar 'clock-and-wavefront'(1-3) mechanism operates to control somitogenesis; in all of them, somitogenesis is brought to an end through a process in which the presomitic mesoderm, having first increased in size, gradually shrinks until it is exhausted, terminating somite formation. In snake embryos, however, the segmentation clock rate is much faster relative to developmental rate than in other amniotes, leading to a greatly increased number of smaller-sized somites.
引用
收藏
页码:335 / 339
页数:5
相关论文
共 31 条
[1]   Wnt3A plays a major role in the segmentation clock controlling somitogenesis [J].
Aulehla, A ;
Wehrle, C ;
Brand-Saberi, B ;
Kemler, R ;
Gossler, A ;
Kanzler, B ;
Herrmann, BG .
DEVELOPMENTAL CELL, 2003, 4 (03) :395-406
[2]   A β-catenin gradient links the clock and wavefront systems in mouse embryo segmentation [J].
Aulehla, Alexander ;
Wiegraebe, Winfried ;
Baubet, Valerie ;
Wahl, Matthias B. ;
Deng, Chuxia ;
Taketo, Makoto ;
Lewandoski, Mark ;
Pourquie, Olivier .
NATURE CELL BIOLOGY, 2008, 10 (02) :186-U56
[3]   PARAXIS - A BASIC HELIX-LOOP-HELIX PROTEIN EXPRESSED IN PARAXIAL MESODERM AND DEVELOPING SOMITES [J].
BURGESS, R ;
CSERJESI, P ;
LIGON, KL ;
OLSON, EN .
DEVELOPMENTAL BIOLOGY, 1995, 168 (02) :296-306
[4]   Two distinct sources for a population of maturing axial progenitors [J].
Cambray, Noemi ;
Wilson, Valerie .
DEVELOPMENT, 2007, 134 (15) :2829-2840
[5]   CLOCK AND WAVEFRONT MODEL FOR CONTROL OF NUMBER OF REPEATED STRUCTURES DURING ANIMAL MORPHOGENESIS [J].
COOKE, J ;
ZEEMAN, EC .
JOURNAL OF THEORETICAL BIOLOGY, 1976, 58 (02) :455-476
[6]   Control of the segmentation process by graded MAPK/ERK activation in the chick embryo [J].
Delfini, MC ;
Dubrulle, J ;
Malapert, P ;
Chal, J ;
Pourquié, O .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (32) :11343-11348
[7]   Segmental patterning of the vertebrate embryonic axis [J].
Dequeant, Mary-Lee ;
Pourquie, Olivier .
NATURE REVIEWS GENETICS, 2008, 9 (05) :370-382
[8]   A complex oscillating network of signaling genes underlies the mouse segmentation clock [J].
Dequeant, Mary-Lee ;
Glynn, Earl ;
Gaudenz, Karin ;
Wahl, Matthias ;
Chen, Jie ;
Mushegian, Arcady ;
Pourquie, Olivier .
SCIENCE, 2006, 314 (5805) :1595-1598
[9]  
Diez del Corral R, 2003, NEURON, V40, P65
[10]   FGF signaling controls somite boundary position and regulates segmentation clock control of spatiotemporal Hox gene activation [J].
Dubrulle, J ;
McGrew, MJ ;
Pourquié, O .
CELL, 2001, 106 (02) :219-232