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ABSTRACT Homeotic (Hox) genes specify the differential identity of segments along the body axis of insects. Changes in the segmental organization of arthropod bodies may therefore be driven
by changes in the function of Hox genes1,2,3, but so far this has been difficult to demonstrate. We show here that changes in the expression pattern of the Hox genes _Ubx_ and _AbdA_ in
different crustaceans correlate well with the modification of their anterior thoracic limbs into feeding appendages (maxillipeds). Our observations provide direct evidence that major
morphological changes in arthropod body plans are associated with changes in Hox gene regulation. They suggest that homeotic changes1,4 may play a role in the normal process of adaptive
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Contact customer support SIMILAR CONTENT BEING VIEWED BY OTHERS EXITES IN CAMBRIAN ARTHROPODS AND HOMOLOGY OF ARTHROPOD LIMB BRANCHES Article Open access 30 July 2021 EVOLUTION OF
STICKLEBACK SPINES THROUGH INDEPENDENT _CIS_-REGULATORY CHANGES AT _HOXDB_ Article Open access 01 September 2022 NON-COLLINEAR HOX GENE EXPRESSION IN BIVALVES AND THE EVOLUTION OF
MORPHOLOGICAL NOVELTIES IN MOLLUSKS Article Open access 11 February 2021 REFERENCES * Lewis, E. B. Agene complex controlling segmentation in _Drosophila_. _Nature_ 276, 567–570 (1978). ADS
Google Scholar * Raff, R. A. & Kaufman, T. C. _Embryos, Genes, and Evolution_ (Indiana University Press, Bloomington, 1991). Google Scholar * Akam, M., Dawson, I. & Tear, G.
Homeotic genes and the control of segment diversity. _Development_ 104 (SUPPL.), 123–133 (1988). Google Scholar * Bateson, W. _Materials for the Study of Variation, Treated with Especial
Regard to Discontinuity in the Origin of Species_ (Macmillan, London, 1894). Google Scholar * Averof, M. & Akam, M. _HOM/Hox_ genes of _Artemia_: implications for the origin of insect
and crustacean body plans. _Curr. Biol._ 3, 73–78 (1993). Article CAS Google Scholar * Averof, M., Dawes, R. & Ferrier, D. Diversification of arthropod _Hox_ genes as a paradigm for
the evolution of gene functions. _Sem. Dev. Cell. Biol._ 7, 539–551 (1996). Article CAS Google Scholar * Averof, M. & Akam, M. _Hox_ genes and the diversification of insect and
crustacean body plans. _Nature_ 376, 420–423 (1995). Article ADS CAS Google Scholar * Panganiban, G., Sebring, A., Nagy, L. & Carroll, S. The development of crustacean limbs and the
evolution of arthropods. _Science_ 270, 1363–1366 (1995). Article ADS CAS Google Scholar * Calman, W. T. _Crustacea_ (Black, London, 1909). Google Scholar * Giesbrecht, W. in
_Handwörterbuch der Naturwissecschaften_ (ed. Dittler, R.) 800–840 (Fischer, Jena, 1931). Google Scholar * Schram, F. R. _Crustacea_ (Oxford University Press, Oxford, 1986). Google Scholar
* Brusca, R. C. & Brusca, G. J. _Invertebrates_ 1–922 (Sinauer, Sunderland Massachusetts, 1990). Google Scholar * Kelsh, R., Weinzierl, R. O. J., White, R. A. H. & Akam, M.
Homeotic gene expression in the locust _Schistocerca_: an antibody that detects conserved epitopes in _Ultrabithorax_ and _Abdominal-A_ proteins. _Dev. Genet._ 15, 19–31 (1994). Article CAS
Google Scholar * McGinnis, W. & Krumlauf, R. Homeobox genes and axial patterning. _Cell_ 68, 283–302 (1992). Article CAS Google Scholar * Akam, M. _Hox_ genes and the evolution of
diverse body plans. _Phil. Trans. R. Soc. Lond. B_ 349, 313–319 (1995). Article ADS CAS Google Scholar * Burke, A. C., Nelson, C. E., Morgan, B. A. & Tabin, C. Hox genes and the
evolution of vertebral axial morphology. _Development_ 121, 333–346 (1995). CAS PubMed Google Scholar * Gaunt, S. J. Conservation in the Hox code during morphological evolution. _Int. J.
Dev. Biol._ 38, 549–552 (1994). CAS PubMed Google Scholar * Castelli-Gair, J., Greig, S., Micklem, G. & Akam, M. Dissecting the temporal requirements for homeotic gene function.
_Development_ 120, 1983–1995 (1994). CAS PubMed Google Scholar * Castelli-Gair, J. & Akam, M. How the Hox gene _Ultrabithorax_ specifies two different segments: the significance of
spatial and temporal regulation within metemeres. _Development_ 121, 2973–2982 (1995). CAS PubMed Google Scholar * Salser, S. J. & Kenyon, C. A. _C. elegans_ Hox gene switches on,
off, on, and off again to regulate proliferation, differentiation, and morphogenesis. _Development_ 122, 1651–1661 (1996). CAS PubMed Google Scholar * Briggs, D. E. G. The morphology,
mode of life, and affinities of _Canadaspis perfecta_ (Crustacea, Phyllocarida), Middle Cambrian, Burgess Shale, British Columbia. _Phil. Trans. R. Soc. Lond. B_ 281, 439–487 (1978). Article
ADS Google Scholar * Muller, K. J. & Walossek, D. External morphology and larval development of the Upper Cambrian maxillopod _Bredocaris admirabilis_. _Foss. Strat._ 23, 1–70
(1988). Google Scholar * Walossek, D. The Upper Cambrian _Rehbachiella_ and the phylogeny of Branchiopoda and Crustacea. _Foss. Strat._ 32, 1–202 (1993). Google Scholar * Wagner, G. P. The
biological homology concept. _Annu. Rev. Ecol. Syst._ 20, 51–69 (1989). Article Google Scholar * Patel, N. H., Kornberg, T. B. & Goodman, C. S. Expression of _engrailed_ during
segmentation in grasshopper and crayfish. _Development_ 107, 201–212 (1989). CAS PubMed Google Scholar * Patel, N. H. in _Methods in Cell Biology, 44. Drosophila Melanogaster: Practical
Uses in Cell Biology_ (eds Goldstein, L. S. B. & Fyrberg, E.) 445–487 (Academic, New York, 1994). Google Scholar Download references ACKNOWLEDGEMENTS We thank M. Akam and F. Ferrari for
discussion; K. Rützler and the Smithsonian Institution for hosting our collecting expeditions at Carrie Bow Caye in Belize; R. White for the FP6.87 antibody; G. Wyngaard for _Mesocyclops_;
E. Chang for _Homarus_ embryos; M. Sepanski for help with electron microscopy; A. Crittenden and L. Brown for technical assistance; and M. Palopoli, R. Chasan and S. Cohen for comments on
the manuscript. This work was supported by the Wellcome Trust (M.A.), the Carnegie Institution of Washington, and the Howard Hughes Medical Institute (N.H.P.). AUTHOR INFORMATION Author
notes * Michalis Averof Present address: EMBL, Meyerhofstrasse 1, 69117, Heidelberg, Germany AUTHORS AND AFFILIATIONS * Wellcome/CRC Institute, Tennis Court Road, CB2 1QR, Cambridge, UK
Michalis Averof & Nipam H. Patel * HHMI, University of Chicago, MC1028, N-101, 5841 South Maryland Avenue, 60637, Illinois, Chicago, USA Nipam H. Patel Authors * Michalis Averof View
author publications You can also search for this author inPubMed Google Scholar * Nipam H. Patel View author publications You can also search for this author inPubMed Google Scholar
CORRESPONDING AUTHOR Correspondence to Nipam H. Patel. RIGHTS AND PERMISSIONS Reprints and permissions ABOUT THIS ARTICLE CITE THIS ARTICLE Averof, M., Patel, N. Crustacean appendage
evolution associated with changes in Hox gene expression. _Nature_ 388, 682–686 (1997). https://doi.org/10.1038/41786 Download citation * Received: 25 March 1997 * Accepted: 10 June 1997 *
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