@article {4404, title = {Comprehensive survey of developmental genes in the pea aphid, Acyrthosiphon pisum: frequent lineage-specific duplications and losses of developmental genes.}, journal = {Insect Molecular Biology}, volume = {19 Suppl 2}, year = {2010}, month = {2010 Mar}, pages = {47-62}, abstract = {

Aphids exhibit unique attributes, such as polyphenisms and specialized cells to house endosymbionts, that make them an interesting system for studies at the interface of ecology, evolution and development. Here we present a comprehensive characterization of the developmental genes in the pea aphid, Acyrthosiphon pisum, and compare our results to other sequenced insects. We investigated genes involved in fundamental developmental processes such as establishment of the body plan and organogenesis, focusing on transcription factors and components of signalling pathways. We found that most developmental genes were well conserved in the pea aphid, although many lineage-specific gene duplications and gene losses have occurred in several gene families. In particular, genetic components of transforming growth factor beta (TGFbeta) Wnt, JAK/STAT (Janus kinase/signal transducer and activator of transcription) and EGF (Epidermal Growth Factor) pathways appear to have been significantly modified in the pea aphid.

}, keywords = {Amino Acid, Amino Acid Sequence, Animals, Aphids, Body Patterning, Cytoplasmic and Nuclear, Female, Gene Deletion, Gene Duplication, Genes, Genome, Homeobox, Insect, Insect Proteins, Male, Molecular Sequence Data, Peas, Phylogeny, Receptors, Sequence Homology, Signal Transduction, Transcription Factors}, issn = {1365-2583}, doi = {10.1111/j.1365-2583.2009.00944.x}, author = {Shigenobu, S and Bickel, R D and Brisson, J A and Butts, T and Chang, C-C and Christiaens, O and Davis, G K and Duncan, E J and Ferrier, D E K and Iga, M and Janssen, R and Lin, G-W and Lu, H-L and McGregor, A P and Miura, T and Smagghe, G and Smith, J M and van der Zee, M and Velarde, R A and Wilson, M J and Dearden, P K and Stern, D L} } @article {4403, title = {A full-length cDNA resource for the pea aphid, acyrthosiphon pisum.}, journal = {Insect Molecular Biology}, volume = {19 Suppl 2}, year = {2010}, month = {2010 Mar}, pages = {23-31}, abstract = {

Large collections of full-length cDNAs are important resources for genome annotation and functional genomics. We report the creation of a collection of 50 599 full-length cDNA clones from the pea aphid, Acyrthosiphon pisum. Sequencing from 5{\textquoteright} and 3{\textquoteright} ends of the clones generated 97 828 high-quality expressed sequence tags, representing approximately 9000 genes. These sequences were imported to AphidBase and are shown to play crucial roles in both automatic gene prediction and manual annotation. Our detailed analyses demonstrated that the full-length cDNAs can further improve gene models and can even identify novel genes that are not included in the current version of the official gene set. This full-length cDNA collection can be utilized for a wide variety of functional studies, serving as a community resource for the study of the functional genomics of the pea aphid.

}, keywords = {3{\textquoteright} Untranslated Regions, 5{\textquoteright} Untranslated Regions, Animals, Aphids, Base Sequence, Complementary, DNA, DNA Primers, Expressed Sequence Tags, Gene Library, Genetic, Genome, Host-Pathogen Interactions, Insect, Models, Peas}, issn = {1365-2583}, doi = {10.1111/j.1365-2583.2009.00946.x}, author = {Shigenobu, S and Richards, S and Cree, A G and Morioka, M and Fukatsu, T and Kudo, T and Miyagishima, S and Gibbs, R A and Stern, D L and Nakabachi, A} } @article {45747, title = {Wing dimorphism in aphids.}, journal = {Heredity (Edinb)}, volume = {97}, year = {2006}, month = {2006 Sep}, pages = {192-9}, abstract = {

Many species of insects display dispersing and nondispersing morphs. Among these, aphids are one of the best examples of taxa that have evolved specialized morphs for dispersal versus reproduction. The dispersing morphs typically possess a full set of wings as well as a sensory and reproductive physiology that is adapted to flight and reproducing in a new location. In contrast, the nondispersing morphs are wingless and show adaptations to maximize fecundity. In this review, we provide an overview of the major features of the aphid wing dimorphism. We first provide a description of the dimorphism and an overview of its phylogenetic distribution. We then review what is known about the mechanisms underlying the dimorphism and end by discussing its evolutionary aspects.

}, keywords = {Animals, Aphids, Biological Evolution, Female, Hormones, Male, Polymorphism, Genetic, Wing}, issn = {0018-067X}, doi = {10.1038/sj.hdy.6800863}, author = {Braendle, C and Davis, G K and Brisson, J A and Stern, D L} } @article {45759, title = {Genetic mapping of aphicarus -- a sex-linked locus controlling a wing polymorphism in the pea aphid (Acyrthosiphon pisum).}, journal = {Heredity (Edinb)}, volume = {94}, year = {2005}, month = {2005 Apr}, pages = {435-42}, abstract = {

We have initiated research to determine the genetic basis of a male wing polymorphism in the pea aphid Acyrthosiphon pisum (Hemiptera: Aphididae). Previous studies showed that this polymorphism is controlled by a single biallelic locus, which we name aphicarus (api), on the X chromosome. Our objectives were to confirm that api segregates as a polymorphism of a single gene on the X chromosome, and to obtain molecular markers flanking api that can be used as a starting point for high-resolution genetic and physical mapping of the target region, which will ultimately allow the cloning of api. We have established an F2 population segregating for api and have generated X-linked AFLP markers. The segregation pattern of api in the F2 population shows that the male wing polymorphism segregates as a polymorphism of a single gene, or set of closely linked genes on the X chromosome. Using a subset of 78 F2 males, we have constructed a linkage map of the chromosomal region encompassing api using seven AFLP markers. The map spans 74.1 cM and we have mapped api to an interval of 10 cM. In addition, we confirmed X linkage of our AFLP markers and api by using one X-linked marker developed in an earlier study. Our study presents the first mapping of a gene with known function in aphids, and the results indicate that target gene mapping in aphids is feasible.

}, keywords = {Animals, Aphids, Chromosome Mapping, Genetic Markers, Linkage Disequilibrium, Male, Polymorphism, Genetic, Quantitative Trait Loci, Random Amplified Polymorphic DNA Technique, Wing, X Chromosome}, issn = {0018-067X}, doi = {10.1038/sj.hdy.6800633}, author = {Braendle, C and Caillaud, M C and Stern, D L} } @article {45771, title = {Divergence of larval morphology between Drosophila sechellia and its sibling species caused by cis-regulatory evolution of ovo/shaven-baby.}, journal = {Proc Natl Acad Sci U S A}, volume = {97}, year = {2000}, month = {2000 Apr 25}, pages = {4530-4}, abstract = {

We report an extreme morphological difference between Drosophila sechellia and related species of the pattern of hairs on first-instar larvae. On the dorsum of most species, the posterior region of the anterior compartment of most segments is covered by a carpet of fine hairs. In D. sechellia, these hairs have been lost and replaced with naked cuticle. Genetic mapping experiments and interspecific complementation tests indicate that this difference is caused, in its entirety, by evolution at the ovo/shaven-baby locus. The pattern of expression of the ovo/shaven-baby transcript is correlated with this morphological change. The altered dorsal cuticle pattern is probably caused by evolution of the cis-regulatory region of ovo/shaven-baby in the D. sechellia lineage.

}, keywords = {Animals, Biological Evolution, Body Patterning, Crosses, Genetic, DNA-Binding Proteins, Drosophila, Drosophila melanogaster, Drosophila Proteins, Evolution, Molecular, Female, Genes, Insect, Genetic Complementation Test, Larva, Male, Phylogeny, Species Specificity, Transcription Factors, X Chromosome}, issn = {0027-8424}, author = {Sucena, E and Stern, D L} } @article {45769, title = {Evolutionary biology. The problem of variation.}, journal = {Nature}, volume = {408}, year = {2000}, month = {2000 Nov 30}, pages = {529, 531}, keywords = {Animals, Biological Evolution, DNA, DNA-Binding Proteins, Drosophila melanogaster, Drosophila Proteins, Evolution, Molecular, Female, Gene Expression Regulation, Developmental, Genetic Variation, Male, Mutation, Pigmentation, Sex Characteristics, Sexual Behavior, Animal, Transcription Factors}, issn = {0028-0836}, doi = {10.1038/35046183}, author = {Stern, D L} } @article {45770, title = {Evolutionary developmental biology and the problem of variation.}, journal = {Evolution}, volume = {54}, year = {2000}, month = {2000 Aug}, pages = {1079-91}, abstract = {

One of the oldest problems in evolutionary biology remains largely unsolved. Which mutations generate evolutionarily relevant phenotypic variation? What kinds of molecular changes do they entail? What are the phenotypic magnitudes, frequencies of origin, and pleiotropic effects of such mutations? How is the genome constructed to allow the observed abundance of phenotypic diversity? Historically, the neo-Darwinian synthesizers stressed the predominance of micromutations in evolution, whereas others noted the similarities between some dramatic mutations and evolutionary transitions to argue for macromutationism. Arguments on both sides have been biased by misconceptions of the developmental effects of mutations. For example, the traditional view that mutations of important developmental genes always have large pleiotropic effects can now be seen to be a conclusion drawn from observations of a small class of mutations with dramatic effects. It is possible that some mutations, for example, those in cis-regulatory DNA, have few or no pleiotropic effects and may be the predominant source of morphological evolution. In contrast, mutations causing dramatic phenotypic effects, although superficially similar to hypothesized evolutionary transitions, are unlikely to fairly represent the true path of evolution. Recent developmental studies of gene function provide a new way of conceptualizing and studying variation that contrasts with the traditional genetic view that was incorporated into neo-Darwinian theory and population genetics. This new approach in developmental biology is as important for microevolutionary studies as the actual results from recent evolutionary developmental studies. In particular, this approach will assist in the task of identifying the specific mutations generating phenotypic variation and elucidating how they alter gene function. These data will provide the current missing link between molecular and phenotypic variation in natural populations.

}, keywords = {Animals, Biological Evolution, Evolution, Molecular, Genetic Variation, Genome, Mutation, Phenotype}, issn = {0014-3820}, author = {Stern, D L} } @article {45772, title = {The developmental basis for allometry in insects.}, journal = {Development}, volume = {126}, year = {1999}, month = {1999 Mar}, pages = {1091-101}, abstract = {

Within all species of animals, the size of each organ bears a specific relationship to overall body size. These patterns of organ size relative to total body size are called static allometry and have enchanted biologists for centuries, yet the mechanisms generating these patterns have attracted little experimental study. We review recent and older work on holometabolous insect development that sheds light on these mechanisms. In insects, static allometry can be divided into at least two processes: (1) the autonomous specification of organ identity, perhaps including the approximate size of the organ, and (2) the determination of the final size of organs based on total body size. We present three models to explain the second process: (1) all organs autonomously absorb nutrients and grow at organ-specific rates, (2) a centralized system measures a close correlate of total body size and distributes this information to all organs, and (3) autonomous organ growth is combined with feedback between growing organs to modulate final sizes. We provide evidence supporting models 2 and 3 and also suggest that hormones are the messengers of size information. Advances in our understanding of the mechanisms of allometry will come through the integrated study of whole tissues using techniques from development, genetics, endocrinology and population biology.

}, keywords = {Animals, Biological Evolution, Body Constitution, Insect Hormones, Insects, Metamorphosis, Biological, Organ Size, Vertebrates}, issn = {0950-1991}, author = {Stern, D L and Emlen, D J} } @article {45773, title = {A role of Ultrabithorax in morphological differences between Drosophila species.}, journal = {Nature}, volume = {396}, year = {1998}, month = {1998 Dec 3}, pages = {463-6}, abstract = {

The mechanisms underlying the evolution of morphology are poorly understood. Distantly related taxa sometimes exhibit correlations between morphological differences and patterns of gene expression, but such comparisons cannot establish how mechanisms evolve to generate diverse morphologies. Answers to these questions require resolution of the nature of developmental evolution within and between closely related species. Here I show how the detailed regulation of the Hox gene Ultrabithorax patterns trichomes on the posterior femur of the second leg in Drosophila melanogaster, and that evolution of Ultrabithorax has contributed to divergence of this feature among closely related species. The cis-regulatory regions of Ultrabithorax, and not the protein itself, appear to have evolved. This study provides experimental evidence that cis-regulatory evolution is one way in which conserved proteins have promoted morphological diversity.

}, keywords = {Alleles, Animals, Crosses, Genetic, DNA-Binding Proteins, Drosophila, Drosophila melanogaster, Drosophila Proteins, Evolution, Molecular, Extremities, Female, Gene Expression, Genes, Insect, Homeodomain Proteins, Insect Proteins, Male, Molecular Sequence Data, Species Specificity, Transcription Factors}, issn = {0028-0836}, doi = {10.1038/24863}, author = {Stern, D L} } @article {45774, title = {The evolution of soldiers in aphids.}, journal = {Biol Rev Camb Philos Soc}, volume = {71}, year = {1996}, month = {1996 Feb}, pages = {27-79}, abstract = {

1. Defensive individuals, termed soldiers, have recently been discovered in aphids, Soldiers are typically early instar larvae, and in many species the soldiers are reproductively sterile and morphologically and behaviourally specialized. 2. Since aphids reproduce parthenogenetically, we might expect soldier production to be more widespread in aphids than it is. We suggest that a more useful way to think about these problems is to attempt to understand how a clone (rather than an individual) should invest in defence and reproduction. 3. Known soldiers are currently restricted to two families of aphids, the Pemphigidae and Hormaphididae, although they are distributed widely among genera within these families. We discuss the use of a phylogenetic perspective to aid comparative studies of soldier production and we demonstrate this approach using current estimates of phylogenetic affinities among aphids. We show that the distribution of soldier production requires a minimum of six to nine evolutionary origins plus at least one loss. 4. At least four main types of soldiers exist and we present and discuss this diversity of soldiers. 5. Most soldier-producing species produce soldiers within plant galls and we discuss the importance of galls for the evolution of soldiers. 6. We summarize the evidence on the interactions between soldiers and predators and between soldier-producing aphids and ants. 7. We present an optimality model for soldier investment strategies to help guide investigations of the ecological factors selecting for soldiers. 8. The proximate mechanisms of soldier production are currently very poorly understood and we suggest several avenues for further research.

}, keywords = {Animals, Aphids, Biological Evolution, Infertility, Models, Biological, Reproduction}, issn = {1464-7931}, author = {Stern, D L and Foster, W A} } @article {45775, title = {A phylogenetic analysis of soldier evolution in the aphid family Hormaphididae.}, journal = {Proc Biol Sci}, volume = {256}, year = {1994}, month = {1994 May 23}, pages = {203-9}, abstract = {

Aphid soldiers, altruistic larvae that protect the colony from predators, are an example of highly social behaviour in an insect group with a natural history different from the eusocial Hymenoptera and Isoptera. Aphids therefore allow independent tests of theory developed to explain the evolution of eusociality. Although soldiers have been discovered in five tribes from two families, the number and pattern of origins and losses of soldiers is unknown due to a lack of phylogenetic data. Here I present a mtDNA based phylogeny for the Hormaphididae, and test the hypothesis that soldiers in the tribe Cerataphidini produced during two points in the life cycle represent independent origins. The results support this hypothesis. In addition, a minimum of five evolutionary events, either four origins and one loss or five origins, are required to explain the distribution of soldiers in the family. The positions of the origins and losses are well resolved, and this phylogeny provides an historical framework for studies on the causes of soldier aphid evolution.

}, keywords = {Animals, Aphids, Base Sequence, DNA Primers, DNA, Mitochondrial, Electron Transport Complex IV, Genes, Insect, Molecular Sequence Data, Phylogeny, Sequence Homology, Nucleic Acid}, issn = {0962-8452}, doi = {10.1098/rspb.1994.0071}, author = {Stern, D L} } @article {45776, title = {Nonfloral sources of chemicals that attract male euglossine bees (Apidae: Euglossini).}, journal = {J Chem Ecol}, volume = {19}, year = {1993}, month = {1993 Dec}, pages = {3017-27}, abstract = {

We present chemical analysis of four rotten or fungus-infected logs that attracted fragrance-collecting male euglossine bees. Eight of the 10 volatile compounds detected have never been found in the fragrances of orchids pollinated by male euglossine bees. Nonfloral sources of chemicals such as rotting wood may constitute an important fragrance resource for male bees. Since rotten logs produce large quantities of chemicals over long periods of time, such nonfloral sources might be more important than flowers as a source of certain fragrances for some euglossine bee species. Fragrance collecting in euglossine bees might have evolved originally in relation with rotting wood rather than flowers.

}, issn = {0098-0331}, doi = {10.1007/BF00980599}, author = {Whitten, W M and Young, A M and Stern, D L} }