Distal‐less and dachshund pattern both plesiomorphic and apomorphic structures in chelicerates: RNA interference in the harvestman Phalangium opilio (Opiliones)

The discovery of genetic mechanisms that can transform a morphological structure from a plesiomorphic (=primitive) state to an apomorphic (=derived) one is a cardinal objective of evolutionary developmental biology. However, this objective is often impeded for many lineages of interest by limitations in taxonomic sampling, genomic resources, or functional genetic methods. In order to investigate the evolution of appendage morphology within Chelicerata, the putative sister group of the remaining arthropods, we developed an RNA interference (RNAi) protocol for the harvestman Phalangium opilio. We silenced the leg gap genes Distal‐less (Dll) and dachshund (dac) in the harvestman via zygotic injections of double‐stranded RNA (dsRNA), and used in situ hybridization to confirm RNAi efficacy. Consistent with the conserved roles of these genes in patterning the proximo‐distal axis of arthropod appendages, we observed that embryos injected with Dll dsRNA lacked distal parts of appendages and appendage‐like structures, such as the labrum, the chelicerae, the pedipalps, and the walking legs, whereas embryos injected with dac dsRNA lacked the medial podomeres femur and patella in the pedipalps and walking legs. In addition, we detected a role for these genes in patterning structures that do not occur in well‐established chelicerate models (spiders and mites). Dll RNAi additionally results in loss of the preoral chamber, which is formed from pedipalpal and leg coxapophyses, and the ocularium, a dorsal outgrowth bearing the eyes. In one case, we observed that an embryo injected with dac dsRNA lacked the proximal segment of the chelicera, a plesiomorphic podomere that expresses dac in wild‐type embryos. This may support the hypothesis that loss of the cheliceral dac domain underlies the transition to the two‐segmented chelicera of derived arachnids.

[1]  G. Giribet,et al.  Evolution of the chelicera: a dachshund domain is retained in the deutocerebral appendage of Opiliones (Arthropoda, Chelicerata) , 2012, Evolution & development.

[2]  M. Sutton,et al.  Silurian horseshoe crab illuminates the evolution of arthropod limbs , 2012, Proceedings of the National Academy of Sciences.

[3]  P. Sharma,et al.  Hox gene expression in the harvestman Phalangium opilio reveals divergent patterning of the chelicerate opisthosoma , 2012, Evolution & development.

[4]  J. Krüger,et al.  The sejugal furrow in camel spiders and acariform mites , 2012 .

[5]  D. Waloszek,et al.  Functional morphology, ontogeny and evolution of mantis shrimp‐like predators in the Cambrian , 2012 .

[6]  F. W. Smith,et al.  Patterning of the Adult Mandibulate Mouthparts in the Red Flour Beetle, Tribolium castaneum , 2012, Genetics.

[7]  F. W. Smith,et al.  Extent With Modification: Leg Patterning in the Beetle Tribolium castaneum and the Evolution of Serial Homologs , 2012, G3: Genes | Genomes | Genetics.

[8]  A. McGregor,et al.  Novel Function of Distal-less as a Gap Gene during Spider Segmentation , 2011, PLoS genetics.

[9]  P. Sharma,et al.  The evolutionary and biogeographic history of the armoured harvestmen – Laniatores phylogeny based on ten molecular markers, with the description of two new families of Opiliones (Arachnida) , 2011 .

[10]  Sara Khadjeh,et al.  Patterning mechanisms and morphological diversity of spider appendages and their importance for spider evolution. , 2010, Arthropod structure & development.

[11]  Lars Vogt,et al.  A multilocus approach to harvestman (Arachnida: Opiliones) phylogeny with emphasis on biogeography and the systematics of Laniatores , 2010, Cladistics : the international journal of the Willi Hennig Society.

[12]  M. Akam,et al.  Gene expression patterns in an onychophoran reveal that regionalization predates limb segmentation in pan‐arthropods , 2010, Evolution & development.

[13]  J. Dunlop Geological history and phylogeny of Chelicerata. , 2010, Arthropod structure & development.

[14]  Gregor Bucher,et al.  The insect upper lip (labrum) is a nonsegmental appendage‐like structure , 2009, Evolution & development.

[15]  M. Friedrich,et al.  Probing the Drosophila retinal determination gene network in Tribolium (I): The early retinal genes dachshund, eyes absent and sine oculis. , 2009, Developmental biology.

[16]  D. Rose,et al.  Differential recruitment of limb patterning genes during development and diversification of beetle horns , 2009, Proceedings of the National Academy of Sciences.

[17]  Matthias Pechmann,et al.  Appendage patterning in the South American bird spider Acanthoscurria geniculata (Araneae: Mygalomorphae) , 2009, Development Genes and Evolution.

[18]  Nikola-Michael Prpic,et al.  Notch-mediated segmentation of the appendages is a molecular phylotypic trait of the arthropods. , 2009, Developmental biology.

[19]  L. Riddiford,et al.  Larval leg integrity is maintained by Distal-less and is required for proper timing of metamorphosis in the flour beetle, Tribolium castaneum. , 2009, Developmental biology.

[20]  G. Scholtz,et al.  The chelifores of sea spiders (Arthropoda, Pycnogonida) are the appendages of the deutocerebral segment , 2008, Evolution & development.

[21]  Nikola-Michael Prpic,et al.  Gene Silencing via Embryonic RNAi in Spider Embryos. , 2008, CSH protocols.

[22]  M. Little,et al.  High-throughput paraffin section in situ hybridization and dual immunohistochemistry on mouse tissues. , 2008, CSH protocols.

[23]  A. Popadic,et al.  Ubx Regulates Differential Enlargement and Diversification of Insect Hind Legs , 2007, PloS one.

[24]  J. Shultz A phylogenetic analysis of the arachnid orders based on morphological characters , 2007 .

[25]  M. Grbic,et al.  Gene silencing in the spider mite Tetranychus urticae: dsRNA and siRNA parental silencing of the Distal-less gene , 2007, Development Genes and Evolution.

[26]  G. Edgecombe,et al.  The evolution of arthropod heads: reconciling morphological, developmental and palaeontological evidence , 2006, Development Genes and Evolution.

[27]  D. Rose,et al.  Conservation, innovation, and the evolution of horned beetle diversity , 2006, Development Genes and Evolution.

[28]  Céline Clabaut,et al.  Homology of arthropod anterior appendages revealed by Hox gene expression in a sea spider , 2006, Nature.

[29]  Nikola-Michael Prpic,et al.  Formation of the arthropod labrum by fusion of paired and rotated limb-bud-like primordia , 2006, Zoomorphology.

[30]  M. Martindale,et al.  Neuroanatomy of sea spiders implies an appendicular origin of the protocerebral segment , 2005, Nature.

[31]  T. Kaufman,et al.  Insect appendages and comparative ontogenetics. , 2005, Developmental biology.

[32]  L. Nagy,et al.  Diverse developmental mechanisms contribute to different levels of diversity in horned beetles , 2005, Evolution & development.

[33]  Xiuqiang Wang,et al.  Early Cambrian arthropods—new insights into arthropod head and structural evolution , 2005 .

[34]  N. Patel,et al.  Patterning of the branched head appendages in Schistocerca americana and Tribolium castaneum , 2004, Evolution & development.

[35]  T. Kaufman,et al.  Functional analyses in the hemipteran Oncopeltus fasciatus reveal conserved and derived aspects of appendage patterning in insects. , 2004, Developmental biology.

[36]  T. Williams,et al.  The evolution of patterning of serially homologous appendages in insects , 2004, Development Genes and Evolution.

[37]  G. Boxshall The evolution of arthropod limbs , 2004, Biological reviews of the Cambridge Philosophical Society.

[38]  Najmus S. Mahfooz,et al.  Differential expression patterns of the hox gene are associated with differential growth of insect hind legs. , 2004, Proceedings of the National Academy of Sciences of the United States of America.

[39]  Tetsuya Kojima,et al.  The mechanism of Drosophila leg development along the proximodistal axis , 2004, Development, growth & differentiation.

[40]  Nikola-Michael Prpic,et al.  Expression patterns of leg genes in the mouthparts of the spider Cupiennius salei (Chelicerata: Arachnida) , 2004, Development Genes and Evolution.

[41]  D. Waloszek,et al.  A new 'great-appendage' arthropod from the Lower Cambrian of China and homology of chelicerate chelicerae and raptorial antero-ventral appendages , 2004 .

[42]  M. Klingler,et al.  Gene expression in spider appendages reveals reversal of exd/hth spatial specificity, altered leg gap gene dynamics, and suggests divergent distal morphogen signaling. , 2003, Developmental biology.

[43]  Michael Schoppmeier,et al.  Involvement of Notch and Delta genes in spider segmentation , 2003, Nature.

[44]  T. Kaufman,et al.  Hox genes and the evolution of the arthropod body plan 1 , 2002, Evolution & development.

[45]  G. Budd A palaeontological solution to the arthropod head problem , 2002, Nature.

[46]  P. Dong,et al.  Distal-less and homothorax regulate multiple targets to pattern the Drosophila antenna. , 2002, Development.

[47]  T. Kaufman,et al.  The development and evolution of insect mouthparts as revealed by the expression patterns of gnathocephalic genes , 2002, Evolution & development.

[48]  T. Williams,et al.  A complex role for distal-less in crustacean appendage development. , 2002, Developmental biology.

[49]  C. Rauskolb The establishment of segmentation in the Drosophila leg. , 2001, Development.

[50]  M. Klingler,et al.  Expression of dachshund in wild-type and Distal-less mutant Tribolium corroborates serial homologies in insect appendages , 2001, Development Genes and Evolution.

[51]  Gonzalo Giribet,et al.  Arthropod phylogeny based on eight molecular loci and morphology , 2001, Nature.

[52]  P. Dong,et al.  Proximodistal domain specification and interactions in developing Drosophila appendages. , 2001, Development.

[53]  G. Scholtz,et al.  Distal-less expression in embryos of Limulus polyphemus (Chelicerata, Xiphosura) and Lepisma saccharina (Insecta, Zygentoma) suggests a role in the development of mechanoreceptors, chemoreceptors, and the CNS , 2001, Development Genes and Evolution.

[54]  M. Schoppmeier,et al.  Double-stranded RNA interference in the spider Cupiennius salei: the role of Distal-less is evolutionarily conserved in arthropod appendage formation , 2001, Development Genes and Evolution.

[55]  D. Tautz,et al.  The Short antennae gene of Tribolium is required for limb development and encodes the orthologue of the Drosophila Distal-less protein. , 2001, Development.

[56]  A. Abzhanov,et al.  Homologs of Drosophila appendage genes in the patterning of arthropod limbs. , 2000, Developmental biology.

[57]  M. Telford,et al.  Appendage development in embryos of the oribatid mite Archegozetes longisetosus (Acari, Oribatei, Trhypochthoniidae) , 1999 .

[58]  R. Mann,et al.  Control of the nuclear localization of Extradenticle by competing nuclear import and export signals. , 1999, Genes & development.

[59]  D. Tautz,et al.  A Hox class 3 orthologue from the spider Cupiennius salei is expressed in a Hox-gene-like fashion , 1998, Development Genes and Evolution.

[60]  R. Mann,et al.  Generation of multiple antagonistic domains along the proximodistal axis during Drosophila leg development. , 1998, Development.

[61]  G. Scholtz,et al.  The pattern of Distal-less expression in the mouthparts of crustaceans, myriapods and insects: new evidence for a gnathobasic mandible and the common origin of Mandibulata. , 1998, The International journal of developmental biology.

[62]  R. H. Thomas,et al.  Expression of homeobox genes shows chelicerate arthropods retain their deutocerebral segment. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[63]  W. Wheeler,et al.  The Phylogeny of the Extant Chelicerate Orders , 1998, Cladistics : the international journal of the Willi Hennig Society.

[64]  T. Kaufman,et al.  Molecular evidence for the gnathobasic derivation of arthropod mandibles and for the appendicular origin of the labrum and other structures , 1998, Development Genes and Evolution.

[65]  Richard S. Mann,et al.  Control of antennal versus leg development in Drosophila , 1998, Nature.

[66]  P. Weygoldt REVIEW Evolution and systematics of the Chelicerata , 1998, Experimental & Applied Acarology.

[67]  Hyung Don Ryoo,et al.  Nuclear Translocation of Extradenticle Requires homothorax , which Encodes an Extradenticle-Related Homeodomain Protein , 1997, Cell.

[68]  Thomas Lecuit,et al.  Proximal–distal axis formation in the Drosophila leg , 1997, Nature.

[69]  G. Morata,et al.  Genetic evidence for the subdivision of the arthropod limb into coxopodite and telopodite. , 1996, Development.

[70]  A. Mccarthy Development , 1996, Current Opinion in Neurobiology.

[71]  S. Carroll,et al.  The Development of Crustacean Limbs and the Evolution of Arthropods , 1995, Science.

[72]  R. Parkash,et al.  Parallel selection of ethanol and acetic-acid tolerance in Drosophila melanogaster populations from India , 1994, Genetics Selection Evolution.

[73]  G. Rubin,et al.  dachshund encodes a nuclear protein required for normal eye and leg development in Drosophila. , 1994, Development.

[74]  S. Carroll,et al.  The role of the Distal-less gene in the development and evolution of insect limbs , 1994, Current Biology.

[75]  G. Evans Principles of Acarology , 1992 .

[76]  S. Cohen,et al.  Proximal-distal pattern formation inDrosophila: graded requirement forDistal-less gene activity during limb development , 1989, Roux's archives of developmental biology.

[77]  C. Sunkel,et al.  Brista: a gene involved in the specification and differentiation of distal cephalic and thoracic structures in Drosophila melanogaster , 1987, Roux's archives of developmental biology.

[78]  R. Brinkhurst Evolution in the Annelida , 1982 .

[79]  J. Hedgpeth,et al.  Arthropod Phylogeny with Special Reference to Insects , 1979 .

[80]  N. Platnick,et al.  The Arthropoda: Habits, Functional Morphology, and Evolution , 1978 .

[81]  Ralph I. Smith,et al.  Embryology and Phylogeny in Annelids and Arthropods , 1974 .

[82]  N. Dwyer,et al.  THE NEUROMUSCULAR BASIS OF COXAL FEEDING AND LOCOMOTORY MOVEMENTS IN LIMULUS , 1973 .

[83]  B. Babbitt,et al.  Phylogeny and Systematic Position of Opiliones: A Combined Analysis of Chelicerate Relationships Using Morphological and Molecular Data [X983] (matrix) , 2014 .

[84]  G. Edgecombe,et al.  Reevaluating the arthropod tree of life. , 2012, Annual review of entomology.

[85]  A. Minelli,et al.  Antenna and all gnathal appendages are similarly transformed by homothorax knock-down in the cricket Gryllus bimaculatus. , 2008, Developmental biology.

[86]  R. Pinto‐da‐Rocha,et al.  Harvestmen: the biology of Opiliones , 2007 .

[87]  C. Arango Morphological phylogenetics of the sea spiders (Arthropoda: Pycnogonida) , 2002 .

[88]  G. Scholtz Evolution of developmental patterns in arthropods: the analysis of gene expression and its bearing on morphology and phylogenetics , 2001 .

[89]  P. Weygoldt Evolution and systematics of the Chelicerata , 1999 .

[90]  S. Cohen,et al.  Proximodistal axis formation in the Drosophila leg: subdivision into proximal and distal domains by Homothorax and Distal-less. , 1999, Development.

[91]  T. Williams Distalless expression in crustaceans and the patterning of branched limbs , 1998, Development Genes and Evolution.

[92]  G. Scholtz Cleavage, germ band formation and head segmentation: the ground pattern of the Euarthropoda , 1998 .

[93]  Joel W. Hedgpeth,et al.  The Arthropoda: Habits, Functional Morphology and Evolution , 1979 .

[94]  J. Rempel The Evolution of the Insect Head: the Endless Dispute , 1975 .

[95]  R. Snodgrass Evolution of the annelida onychophora and arthropoda , 1938 .