Abstract
Hox genes are central to the specification of structures along the anterior–posterior body axis1,2, and modifications in their expression have paralleled the emergence of diversity in vertebrate body plans3,4. Here we describe the genomic organization of Hox clusters in different reptiles and show that squamates have accumulated unusually large numbers of transposable elements at these loci5, reflecting extensive genomic rearrangements of coding and non-coding regulatory regions. Comparative expression analyses between two species showing different axial skeletons, the corn snake and the whiptail lizard, revealed major alterations in Hox13 and Hox10 expression features during snake somitogenesis, in line with the expansion of both caudal and thoracic regions. Variations in both protein sequences and regulatory modalities of posterior Hox genes suggest how this genetic system has dealt with its intrinsic collinear constraint to accompany the substantial morphological radiation observed in this group.
This is a preview of subscription content, access via your institution
Access options
Subscribe to this journal
Receive 51 print issues and online access
$199.00 per year
only $3.90 per issue
Buy this article
- Purchase on SpringerLink
- Instant access to full article PDF
Prices may be subject to local taxes which are calculated during checkout
Similar content being viewed by others
Accession codes
Data deposits
Sequences of genes described in this paper are deposited in GenBank under accession numbers GU320304 to GU320335.
References
Kmita, M. & Duboule, D. Organizing axes in time and space; 25 years of colinear tinkering. Science 301, 331–333 (2003)
Deschamps, J. & van Nes, J. Developmental regulation of the Hox genes during axial morphogenesis in the mouse. Development 132, 2931–2942 (2005)
Gaunt, S. J. Conservation in the Hox code during morphological evolution. Int. J. Dev. Biol. 38, 549–552 (1994)
Burke, A. C., Nelson, C. E., Morgan, B. A. & Tabin, C. Hox genes and the evolution of vertebrate axial morphology. Development 121, 333–346 (1995)
Di Poi, N., Montoya-Burgos, J. I. & Duboule, D. Atypical relaxation of structural constraints in Hox gene clusters of the green anole lizard. Genome Res. 19, 602–610 (2009)
Duboule, D. The rise and fall of Hox gene clusters. Development 134, 2549–2560 (2007)
Garcia-Fernandez, J. The genesis and evolution of homeobox gene clusters. Nature Rev. Genet. 6, 881–892 (2005)
Lemons, D. & McGinnis, W. Genomic evolution of Hox gene clusters. Science 313, 1918–1922 (2006)
Cohn, M. J. & Tickle, C. Developmental basis of limblessness and axial patterning in snakes. Nature 399, 474–479 (1999)
Hoffstetter, R. & Gasc, J. P. in Biology of the Reptilia (eds Gans, C., d’A. Bellair, A. & Parsons, T. S.) Vol. 1, 201–310 (Academic, 1969)
Romer, A. S. Osteology of the Reptiles (Krieger Publishing Co., 1997)
Duellman, W. E. & Trueb, L. Biology of Amphibians (Johns Hopkins University Press, 1994)
Gomez, C. et al. Control of segment number in vertebrate embryos. Nature 454, 335–339 (2008)
Woltering, J. M. et al. Axial patterning in snakes and caecilians: evidence for an alternative interpretation of the Hox code. Dev. Biol. 332, 82–89 (2009)
Kmita, M., Tarchini, B., Duboule, D. & Herault, Y. Evolutionary conserved sequences are required for the insulation of the vertebrate Hoxd complex in neural cells. Development 129, 5521–5528 (2002)
Herault, Y., Beckers, J., Kondo, T., Fraudeau, N. & Duboule, D. Genetic analysis of a Hoxd-12 regulatory element reveals global versus local modes of controls in the HoxD complex. Development 125, 1669–1677 (1998)
Feschotte, C. & Pritham, E. J. DNA transposons and the evolution of eukaryotic genomes. Annu. Rev. Genet. 41, 331–368 (2007)
Godwin, A. R. & Capecchi, M. R. Hoxc13 mutant mice lack external hair. Genes Dev. 12, 11–20 (1998)
Carapuço, M., Novoa, A., Bobola, N. & Mallo, M. Hox genes specify vertebral types in the presomitic mesoderm. Genes Dev. 19, 2116–2121 (2005)
Kohlsdorf, T. et al. A molecular footprint of limb loss: sequence variation of the autopodial identity gene Hoxa-13 . J. Mol. Evol. 67, 581–593 (2008)
Muragaki, Y., Mundlos, S., Upton, J. & Olsen, B. Altered growth and branching patterns in synpolydactyly caused by mutations in Hoxd13 . Science 272, 548–551 (1996)
Wellik, D. M. & Capecchi, M. R. Hox10 and Hox11 genes are required to globally pattern the mammalian skeleton. Science 301, 363–367 (2003)
Suemori, H. & Noguchi, S. HoxC cluster genes are dispensable for overall body plan of mouse embryonic development. Dev. Biol. 220, 333–342 (2000)
Young, T. et al. Cdx and Hox genes differentially regulate posterior axial growth in mammalian embryos. Dev. Cell 17, 516–526 (2009)
Lynch, V. J. et al. Adaptive changes in the transcription factor HoxA-11 are essential for the evolution of pregnancy in mammals. Proc. Natl Acad. Sci. USA 105, 14928–14933 (2008)
Scott, V., Morgan, E. A. & Stadler, H. S. Genitourinary functions of Hoxa13 and Hoxd13. J. Biochem. 137, 671–676 (2005)
Wiens, J. J. & Slingluff, J. L. How lizards turn into snakes: a phylogenetic analysis of body-form evolution in anguid lizards. Evolution 55, 2303–2318 (2001)
Raynaud, A. Preliminary data on the body lenghthening and somitogenesis in young embryos of Anguis fragilis L. and of Lacerta viridis Laur. Bull. Soc. Hist. Nat. Toulouse 130, 47–52 (1994)
Zakany, J. & Duboule, D. The role of Hox genes during vertebrate limb development. Curr. Opin. Genet. Dev. 17, 359–366 (2007)
Yang, Z. PAML 4: phylogenetic analysis by maximum likelihood. Mol. Biol. Evol. 24, 1586–1591 (2007)
Acknowledgements
We thank A. Schmitz for sharing squamate tissues; A. Debry and F. Chabaud for technical assistance; and members of the Duboule and Milinkovitch laboratories for discussions and reagents. This work was supported by funds from the University of Geneva and the Federal Institute of Technology in Lausanne, the Swiss National Research Fund, the National Research Center (NCCR) ‘Frontiers in Genetics’, the EU programme ‘Crescendo’ and the ERC grant SystemsHox.ch (to D.D.).
Author Contributions N.D.P. and D.D. designed the experiments and analysed the data. N.D.P. performed the experiments except those involving the tuatara, which were conducted by H.M. J.I.M.B. performed the phylogenetic analyses. M.C.M. produced and prepared snake embryos and O.P. provided snake and lizard embryos. N.D.P. and D.D. wrote the paper, and all co-authors contributed in the form of discussion and critical comments.
Author information
Authors and Affiliations
Corresponding author
Supplementary information
Supplementary Information
This file contains Supplementary Methods, Supplementary Figures 1-8 with Legends and Supplementary Table 1. (PDF 2073 kb)
Rights and permissions
About this article
Cite this article
Di-Poï, N., Montoya-Burgos, J., Miller, H. et al. Changes in Hox genes’ structure and function during the evolution of the squamate body plan. Nature 464, 99–103 (2010). https://doi.org/10.1038/nature08789
Received:
Accepted:
Issue Date:
DOI: https://doi.org/10.1038/nature08789
Comments
By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.