Cited by 104Developmental Biology and Gene RegulationCongenital limb and hand anomaliesGenomics and Chromatin Dynamics

Comparative analysis of genes downstream of the Hoxd cluster in developing digits and external genitalia

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Cobb, John, Duboule, Denis·2005·Development

Abstract

Mammalian Hox genes encode transcription factors that are crucial for proper morphogenesis along the various body axes. Despite their extensive structural and functional characterization, the nature of their target genes remains elusive. We have addressed this question by using DNA microarrays to screen for genes whose expression in developing distal forelimbs and genital eminences was significantly modified in the absence of the full Hoxd gene complement. This comparative approach not only identified specific candidate genes, but also allowed the examination of whether a similar Hox expression pattern in distinct tissues leads to the modulation of the same or different downstream genes. We report here a set of potential target genes, most of which were not previously known to play a role in the early stages of either limb or genital bud development. Interestingly, we find that the majority of these candidate genes are differentially expressed in both structures, although often at different times. This supports the idea that both appendices involve similar genetic controls, both upstream and downstream of the Hox gene family. These results highlight the surprising mechanistic relationship between these rather different body parts and suggest a common developmental strategy to build up the most distal appendicular structures of the body, i.e. the digits and the penis/clitoris.

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Crossref · 10.1242/dev.01885

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  • Studies of direct hox gene targets reveal other regulatory genes and far downstream genes encoding proteins active in apoptosis, cell cycle control, cell adhesion, cell polarity, non-canonical signalling, and cytoskeletal functions.

    “Studies of direct hox gene targets reveal both other regulatory genes and far downstream genes encoding proteins active, e.g., in apoptosis, cell cycle control, cell adhesion, cell polarity, non-canonical signalling, and cytoskeletal functions (Cobb and Duboule, 2005; Hueber and Lohmann, 2008; Pearson et al., 2005).”

    From Evolution of Gene Regulatory Networks Controlling Body Plan Development (2011) · cites this paper as Cobb and Duboule, 2005

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Authors
Cobb, J., & Duboule, D.
Affiliations
University of Geneva (CH)
Venue
Development
Published
2005-07-01
Volume
132
Issue
13
Pages
3055-3067
ISSN
  • 0950-1991 (ISSN-L)
  • 1477-9129
OpenAlex
W1979989586
Cited by
104
References
1
Citations by year
2026: 4 · 2025: 1 · 2024: 2 · 2023: 1 · 2022: 1 · 2021: 3 · 2020: 3 · 2019: 3 · 2017: 2 · 2016: 6 · 2015: 7 · 2014: 6 · 2013: 8 · 2012: 6
FWCI
3.64
Type
journal article
Language
en
Open access
Locations
  • Development (publishedVersion)
  • PubMed (publishedVersion)
  • Infoscience (Ecole Polytechnique Fédérale de Lausanne) (submittedVersion)
  • Infoscience (Ecole Polytechnique Fédérale de Lausanne) (submittedVersion, cc-by-nc-nd)
  • HighWire Press Open Archive (submittedVersion)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Developmental Biology › Congenital limb and hand anomalies
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Chromatin Dynamics
Keywords
Hoxd genes, digit development, external genitalia development, gene expression profiling, transcriptional regulation
MeSH terms
Serum-Glucocorticoid Regulated Kinases, Animals, Extremities, Female, Multigene Family, Genitalia, Female, Genitalia, Male, Male, Membrane Proteins, Nuclear Proteins, Proto-Oncogene Proteins, Transcription Factors, Protein Serine-Threonine Kinases, In Situ Hybridization, Immediate-Early Proteins, Homeodomain Proteins, Gene Expression Regulation, Developmental, Reverse Transcriptase Polymerase Chain Reaction, Oligonucleotide Array Sequence Analysis, Receptor Protein-Tyrosine Kinases, Gene Expression Profiling, Receptor, EphA3, Proto-Oncogene Proteins c-ret, Mice

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