Shaping segments: Hox gene function in the genomic age

被引:110
作者
Hueber, Stefanie D. [2 ]
Lohmann, Ingrid [1 ,2 ]
机构
[1] Heidelberg Univ, NWG Dev Biol, BIOQUANT Zentrum, D-69120 Heidelberg, Germany
[2] AG I Lohmann, Dept Mol Biol, MPI Dev Biol, Tubingen, Germany
关键词
D O I
10.1002/bies.20823
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Despite decades of research, morphogenesis along the various body axes remains one of the major mysteries in developmental biology. A milestone in the field was the realisation that a set of closely related regulators, called Hox genes, specifies the identity of body segments along the anterior-posterior (AP) axis in most animals. Hox genes have been highly conserved throughout metazoan evolution and code for homeodomain-containing transcription factors. Thus, they exert their function mainly through activation or repression of downstream genes. However, while much is known about Hox gene structure and molecular function, only a few target genes have been identified and studied in detail. Our knowledge of Hox downstream genes is therefore far from complete and consequently Hox-controlled morphogenesis is still poorly understood. Genome-wide approaches have facilitated the identification of large numbers of Hox downstream genes both in Drosophila and vertebrates, and represent a crucial step towards a comprehensive understanding of how Hox proteins drive morphological diversification. In this review, we focus on the role of Hox genes in shaping segmental morphologies along the AP axis in Drosophila, discuss some of the conclusions drawn from analyses of large target gene sets and highlight methods that could be used to gain a more thorough understanding of Hox molecular function. In addition, the mechanisms of Hox target gene regulation are considered with special emphasis on recent findings and their implications for Hox protein specificity in the context of the whole organism. BioEssays 30:965-979, 2008. (C) 2008 Wiley Periodicals, Inc.
引用
收藏
页码:965 / 979
页数:15
相关论文
共 123 条
[1]   CELL-TYPE-SPECIFIC MECHANISMS OF TRANSCRIPTIONAL REPRESSION BY THE HOMEOTIC GENE-PRODUCTS UBX AND ABD-A IN DROSOPHILA EMBRYOS [J].
APPEL, B ;
SAKONJU, S .
EMBO JOURNAL, 1993, 12 (03) :1099-1109
[2]  
Bateson W., 1894, Materials for the study of variation
[3]   GENETIC-ANALYSIS OF THE HOMEOTIC GENE-COMPLEX (HOM-C) IN THE BEETLE TRIBOLIUM-CASTANEUM [J].
BEEMAN, RW ;
STUART, JJ ;
HAAS, MS ;
DENELL, RE .
DEVELOPMENTAL BIOLOGY, 1989, 133 (01) :196-209
[4]   A pulse of the Drosophila Hox protein abdominal-A schedules the end of neural proliferation via neuroblast apoptosis [J].
Bello, BC ;
Hirth, F ;
Gould, AP .
NEURON, 2003, 37 (02) :209-219
[5]   Computational identification of developmental enhancers:: conservation and function of transcription factor binding-site clusters in Drosophila melanogaster and Drosophila pseudoobscura -: art. no. R61 [J].
Berman, BP ;
Pfeiffer, BD ;
Laverty, TR ;
Salzberg, SL ;
Rubin, GM ;
Eisen, MB ;
Celniker, SE .
GENOME BIOLOGY, 2004, 5 (09)
[6]   Exploiting transcription factor binding site clustering to identify cis-regulatory modules involved in pattern formation in the Drosophila genome [J].
Berman, BP ;
Nibu, Y ;
Pfeiffer, BD ;
Tomancak, P ;
Celniker, SE ;
Levine, M ;
Rubin, GM ;
Eisen, MB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (02) :757-762
[7]  
Biggin MD, 1997, DEVELOPMENT, V124, P4425
[8]   Physical and genetic interactions link Hox function with diverse transcription factors and cell signaling proteins [J].
Bondos, SE ;
Tan, XX ;
Matthews, KS .
MOLECULAR & CELLULAR PROTEOMICS, 2006, 5 (05) :824-834
[9]  
Bondos SE, 2001, CRIT REV EUKAR GENE, V11, P145
[10]  
Capovilla M, 2001, DEVELOPMENT, V128, P1221