Hox Genes and Segmentation of the Hindbrain and Axial Skeleton

被引:219
作者
Alexander, Tara [1 ]
Nolte, Christof [1 ]
Krumlauf, Robb [1 ]
机构
[1] Stowers Inst Med Res, Kansas City, MO 64110 USA
关键词
rhombomeres; somites; vertebrae; neural crest; global patterning; homeotic transformation; fibroblast growth factor (Fgf); retinoic acid (RA); caudal homeobox gene (Cdx); variant hepatocyte nuclear factor 1 gene (vhnf1); mesoderm; colinearity; ACID RESPONSE ELEMENT; CRANIAL NEURAL CREST; RETINOIC-ACID; MOUSE EMBRYO; ROSTRAL HINDBRAIN; PRIMITIVE STREAK; IN-VIVO; MORPHOGENETIC MOVEMENT; RHOMBOMERE IDENTITY; EPH RECEPTORS;
D O I
10.1146/annurev.cellbio.042308.113423
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Segmentation is an important process that is frequently used during development to segregate groups of cells with distinct features. Segmental compartments provide a mechanism for generating and organizing regional properties along an embryonic axis and within tissues. In vertebrates the development of two major systems, the hindbrain and the paraxial mesoderm, displays overt signs of compartmentalization and depends on the process of segmentation for their functional organization. The hindbrain plays a key role in regulating head development, and it is a complex coordination center for motor activity, breathing rhythms, and many unconscious functions. The paraxial mesoderm generates somites, which give rise to the axial skeleton. The cellular processes of segmentation in these two systems depend on ordered patterns of Hox gene expression as a mechanism for generating a combinatorial code that specifies unique identities of die segments and their derivatives. In this review, we compare and contrast the signaling inputs and transcriptional mechanisms by which Hox gene regulatory networks are established during segmentation in these two different systems.
引用
收藏
页码:431 / 456
页数:26
相关论文
共 150 条
[1]   The retinoic acid-metabolizing enzyme, CYP26A1, is essential for normal hindbrain patterning, vertebral identity, and development of posterior structures [J].
Abu-Abed, S ;
Dollé, P ;
Metzger, D ;
Beckett, B ;
Chambon, P ;
Petkovich, M .
GENES & DEVELOPMENT, 2001, 15 (02) :226-240
[2]  
Akasaka T, 2001, DEVELOPMENT, V128, P1587
[3]   RARγ and Cdx1 interactions in vertebral patterning [J].
Allan, D ;
Houle, M ;
Bouchard, N ;
Meyer, BI ;
Gruss, P ;
Lohnes, D .
DEVELOPMENTAL BIOLOGY, 2001, 240 (01) :46-60
[4]   vHnf1 regulates specification of caudal rhombomere identity in the chick hindbrain [J].
Aragón, F ;
Vázquez-Echeverría, C ;
Ulloa, E ;
Reber, M ;
Cereghini, S ;
Alsina, B ;
Giraldez, F ;
Pujades, C .
DEVELOPMENTAL DYNAMICS, 2005, 234 (03) :567-576
[5]   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
[6]   EXPRESSION OF CDX-2 IN THE MOUSE EMBRYO AND PLACENTA - POSSIBLE ROLE IN PATTERNING OF THE EXTRAEMBRYONIC MEMBRANES [J].
BECK, F ;
ERLER, T ;
RUSSELL, A ;
JAMES, R .
DEVELOPMENTAL DYNAMICS, 1995, 204 (03) :219-227
[7]  
Bel-Vialar S, 2002, DEVELOPMENT, V129, P5103
[8]   Polycomb complexes repress developmental regulators in murine embryonic stem cells [J].
Boyer, LA ;
Plath, K ;
Zeitlinger, J ;
Brambrink, T ;
Medeiros, LA ;
Lee, TI ;
Levine, SS ;
Wernig, M ;
Tajonar, A ;
Ray, MK ;
Bell, GW ;
Otte, AP ;
Vidal, M ;
Gifford, DK ;
Young, RA ;
Jaenisch, R .
NATURE, 2006, 441 (7091) :349-353
[9]   Analysis of TALE superclass homeobox genes (MEIS, PBC, KNOX, Iroquois, TGIF) reveals a novel domain conserved between plants and animals [J].
Burglin, TR .
NUCLEIC ACIDS RESEARCH, 1997, 25 (21) :4173-4180
[10]   Two distinct sources for a population of maturing axial progenitors [J].
Cambray, Noemi ;
Wilson, Valerie .
DEVELOPMENT, 2007, 134 (15) :2829-2840