Pax group III genes and the evolution of insect pair-rule patterning.

Pair-rule genes were identified and named for their role in segmentation in embryos of the long germ insect Drosophila. Among short germ insects these genes exhibit variable expression patterns during segmentation and thus are likely to play divergent roles in this process. Understanding the details of this variation should shed light on the evolution of the genetic hierarchy responsible for segmentation in Drosophila and other insects. We have investigated the expression of homologs of the Drosophila Pax group III genes paired, gooseberry and gooseberry-neuro in short germ flour beetles and grasshoppers. During Drosophila embryogenesis, paired acts as one of several pair-rule genes that define the boundaries of future parasegments and segments, via the regulation of segment polarity genes such as gooseberry, which in turn regulates gooseberry-neuro, a gene expressed later in the developing nervous system. Using a crossreactive antibody, we show that the embryonic expression of Pax group III genes in both the flour beetle Tribolium and the grasshopper Schistocerca is remarkably similar to the pattern in Drosophila. We also show that two Pax group III genes, pairberry1 and pairberry2, are responsible for the observed protein pattern in grasshopper embryos. Both pairberry1 and pairberry2 are expressed in coincident stripes of a one-segment periodicity, in a manner reminiscent of Drosophila gooseberry and gooseberry-neuro. pairberry1, however, is also expressed in stripes of a two-segment periodicity before maturing into its segmental pattern. This early expression of pairberry1 is reminiscent of Drosophila paired and represents the first evidence for pair-rule patterning in short germ grasshoppers or any hemimetabolous insect.

[1]  F. Falciani,et al.  Dax, a locust Hox gene related to fushi-tarazu but showing no pair-rule expression. , 1994, Development.

[2]  P. O’Farrell,et al.  Establishment and refinement of segmental pattern in the Drosophila embryo: spatial control of engrailed expression by pair-rule genes. , 1987, Genes & development.

[3]  D. Tautz,et al.  Expression patterns of hairy, even-skipped, and runt in the spider Cupiennius salei imply that these genes were segmentation genes in a basal arthropod. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[4]  D. Melton,et al.  Bimodal and graded expression of the Xenopus homeobox gene Xhox3 during embryonic development. , 1989, Development.

[5]  M. Noll,et al.  Complex regulation of early paired expression: initial activation by gap genes and pattern modulation by pair-rule genes. , 1993, Development.

[6]  N. Patel The evolution of arthropod segmentation: insights from comparisons of gene expression patterns. , 1994, Development (Cambridge, England). Supplement.

[7]  N. Patel,et al.  repo encodes a glial-specific homeo domain protein required in the Drosophila nervous system. , 1994, Genes & development.

[8]  M. Noll,et al.  Evolution of distinct developmental functions of three Drosophila genes by acquisition of different cis-regulatory regions , 1994, Nature.

[9]  M. Noll Evolution and role of Pax genes. , 1993, Current opinion in genetics & development.

[10]  K. G. Coleman,et al.  Expression of engrailed proteins in arthropods, annelids, and chordates. , 1989, Cell.

[11]  P. Ingham,et al.  Regulation of wingless transcription in the Drosophila embryo. , 1993, Development.

[12]  M. Noll,et al.  Role of the gooseberry gene in Drosophila embryos: maintenance of wingless expression by a wingless‐‐gooseberry autoregulatory loop. , 1993, The EMBO journal.

[13]  N. Patel,et al.  Imaging neuronal subsets and other cell types in whole-mount Drosophila embryos and larvae using antibody probes. , 1994, Methods in cell biology.

[14]  M. Akam,et al.  Early embryo patterning in the grasshopper, Schistocerca gregaria: wingless, decapentaplegic and caudal expression. , 2001, Development.

[15]  M. Noll,et al.  Structure of the segmentation gene paired and the Drosophila PRD gene set as part of a gene network , 1986, Cell.

[16]  Nipam H. Patel,et al.  Pair-rule expression patterns of even-skipped are found in both short- and long-germ beetles , 1994, Nature.

[17]  M. D'Esposito,et al.  EVX2, a human homeobox gene homologous to the even-skipped segmentation gene, is localized at the 5' end of HOX4 locus on chromosome 2. , 1991, Genomics.

[18]  N. Patel,et al.  Expression of engrailed during segmentation in grasshopper and crayfish. , 1989, Development.

[19]  M. Weir,et al.  Functional dissection of the paired segmentation gene in Drosophila embryos. , 1991, Genes & development.

[20]  S. Benzer,et al.  Divergent decapentaplegic expression patterns in compound eye development and the evolution of insect metamorphosis. , 2000, The Journal of experimental zoology.

[21]  Susan J. Brown,et al.  A deficiency of the homeotic complex of the beetle Tribolium , 1991, Nature.

[22]  M. Noll,et al.  Network of interactions among pair-rule genes regulating paired expression during primordial segmentation of Drosophila , 1990, Mechanisms of Development.

[23]  S. Kumar,et al.  Evolution of functional diversification of the paired box (Pax) DNA-binding domains. , 1997, Molecular biology and evolution.

[24]  J. Ahringer,et al.  Posterior patterning by the Caenorhabditis elegans even-skipped homolog vab-7. , 1996, Genes & development.

[25]  N. Patel,et al.  Developmental evolution: insights from studies of insect segmentation. , 1994, Science.

[26]  N. Patel,et al.  Genetic separation of the neural and cuticular patterning functions of gooseberry. , 1997, Development.

[27]  M. Noll,et al.  Structure of two genes at the gooseberry locus related to the paired gene and their spatial expression during Drosophila embryogenesis. , 1987, Genes & development.

[28]  M. Frasch,et al.  Characterization and localization of the even‐skipped protein of Drosophila. , 1987, The EMBO journal.

[29]  C. Rickert,et al.  The homeobox gene repo is required for the differentiation and maintenance of glia function in the embryonic nervous system of Drosophila melanogaster. , 1995, Development.

[30]  M. Telford,et al.  Evidence for the derivation of the Drosophila fushi tarazu gene from a Hox gene orthologous to lophotrochozoan Lox5 , 2000, Current Biology.

[31]  D. Tautz,et al.  A conserved mode of head segmentation in arthropods revealed by the expression pattern of Hox genes in a spider. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[32]  D. Duboule,et al.  Developmental expression of the mouse Evx-2 gene: relationship with the evolution of the HOM/Hox complex. , 1994, Development (Cambridge, England). Supplement.

[33]  N. Patel,et al.  Analysis of the gooseberry locus in Drosophila embryos: gooseberry determines the cuticular pattern and activates gooseberry neuro. , 1993, Development.

[34]  P. Gruss,et al.  A murine even‐skipped homologue, Evx 1, is expressed during early embryogenesis and neurogenesis in a biphasic manner. , 1990, The EMBO journal.

[35]  Gregor Bucher,et al.  Pair-rule and gap gene mutants in the flour beetle Tribolium castaneum , 1998, Development Genes and Evolution.

[36]  Susan J. Brown,et al.  Embryonic expression of the single Tribolium engrailed homolog. , 1994, Developmental genetics.

[37]  M. Noll,et al.  The functional conservation of proteins in evolutionary alleles and the dominant role of enhancers in evolution. , 1996, The EMBO journal.

[38]  K. Anderson,et al.  Embryonic patterning mutants of Tribolium castaneum. , 1996, Development.

[39]  K. Sander Specification of the Basic Body Pattern in Insect Embryogenesis1 , 1976 .

[40]  K. Anderson,et al.  Altered patterns of gene expression in Tribolium segmentation mutants. , 1998, Developmental genetics.

[41]  Nipam H. Patel,et al.  Changing role of even-skipped during the evolution of insect pattern formation , 1992, Nature.

[42]  L. Nagy,et al.  The role of wingless in the development of multibranched crustacean limbs , 1999, Development Genes and Evolution.

[43]  S. Lall,et al.  Grasshopper hunchback expression reveals conserved and novel aspects of axis formation and segmentation. , 2001, Development.

[44]  M. Fujioka,et al.  Early even-skipped stripes act as morphogenetic gradients at the single cell level to establish engrailed expression. , 1995, Development.

[45]  D. Hayward,et al.  Pax gene diversity in the basal cnidarian Acropora millepora (Cnidaria, Anthozoa): implications for the evolution of the Pax gene family. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[46]  A. Myers,et al.  High-expression vectors with multiple cloning sites for construction of trpE fusion genes: pATH vectors. , 1991, Methods in enzymology.

[47]  Susan J. Brown,et al.  The beetle Tribolium castaneum has a fushi tarazu homolog expressed in stripes during segmentation. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[48]  C. Nüsslein-Volhard,et al.  Mutations affecting segment number and polarity in Drosophila , 1980, Nature.

[49]  H. Keshishian,et al.  Quantitative staging of embryonic development of the grasshopper, Schistocerca nitens. , 1979, Journal of embryology and experimental morphology.

[50]  G. Ruvkun,et al.  Pax genes in Caenorhabditis elegans: a new twist. , 1999, Trends in genetics : TIG.