38 research outputs found

    Integration of Morphological Data into Molecular Phylogenetic Analysis: Toward the Identikit of the Stylasterid Ancestor

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    Stylasteridae is a hydroid family including 29 worldwide-distributed genera, all provided with a calcareous skeleton. They are abundant in shallow and deep waters and represent an important component of marine communities. In the present paper, we studied the evolution of ten morphological characters, currently used in stylasterid taxonomy, using a phylogenetic approach. Our results indicate that stylasterid morphology is highly plastic and that many events of independent evolution and reversion have occurred. Our analysis also allows sketching a possible identikit of the stylasterid ancestor. It had calcareous skeleton, reticulate-granular coenosteal texture, polyps randomly arranged, gastrostyle, and dactylopore spines, while lacking a gastropore lip and dactylostyles. If the ancestor had single or double/multiple chambered gastropore tube is uncertain. These data suggest that the ancestor was similar to the extant genera Cyclohelia and Stellapora. Our investigation is the first attempt to integrate molecular and morphological information to clarify the stylasterid evolutionary scenario and represents the first step to infer the stylasterid ancestor morphology. \ua9 2016 Puce et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited

    Back to Water: Signature of Adaptive Evolution in Cetacean Mitochondrial tRNAs

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    Abstract The mitochondrion is the power plant of the eukaryotic cell, and tRNAs are the fundamental components of its translational machinery. In the present paper, the evolution of mitochondrial tRNAs was investigated in the Cetacea, a clade of Cetartiodactyla that retuned to water and thus had to adapt its metabolism to a different medium than that of its mainland ancestors. Our analysis focussed on identifying the factors that influenced the evolution of Cetacea tRNA double-helix elements, which play a pivotal role in the formation of the secondary and tertiary structures of each tRNA and consequently manipulate the whole translation machinery of the mitochondrion. Our analyses showed that the substitution pathways in the stems of different tRNAs were influenced by various factors, determining a molecular evolution that was unique to each of the 22 tRNAs. Our data suggested that the composition, AT-skew, and GC-skew of the tRNA stems were the main factors influencing the substitution process. In particular, the range of variation and the fluctuation of these parameters affected the fate of single tRNAs. Strong heterogeneity was observed among the different species of Cetacea. Finally, it appears that the evolution of mitochondrial tRNAs was also shaped by the environments in which the Cetacean taxa differentiated. This latter effect was particularly evident in toothed whales that either live in freshwater or are deep divers

    The mitochondrial genome of the ascalaphid owlfly Libelloides macaronius and comparative evolutionary mitochondriomics of neuropterid insects

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    BACKGROUND: The insect order Neuroptera encompasses more than 5,700 described species. To date, only three neuropteran mitochondrial genomes have been fully and one partly sequenced. Current knowledge on neuropteran mitochondrial genomes is limited, and new data are strongly required. In the present work, the mitochondrial genome of the ascalaphid owlfly Libelloides macaronius is described and compared with the known neuropterid mitochondrial genomes: Megaloptera, Neuroptera and Raphidioptera. These analyses are further extended to other endopterygotan orders. RESULTS: The mitochondrial genome of L. macaronius is a circular molecule 15,890 bp long. It includes the entire set of 37 genes usually present in animal mitochondrial genomes. The gene order of this newly sequenced genome is unique among Neuroptera and differs from the ancestral type of insects in the translocation of trnC. The L. macaronius genome shows the lowest A+T content (74.50%) among known neuropterid genomes. Protein-coding genes possess the typical mitochondrial start codons, except for cox1, which has an unusual ACG. Comparisons among endopterygotan mitochondrial genomes showed that A+T content and AT/GC-skews exhibit a broad range of variation among 84 analyzed taxa. Comparative analyses showed that neuropterid mitochondrial protein-coding genes experienced complex evolutionary histories, involving features ranging from codon usage to rate of substitution, that make them potential markers for population genetics/phylogenetics studies at different taxonomic ranks. The 22 tRNAs show variable substitution patterns in Neuropterida, with higher sequence conservation in genes located on the α strand. Inferred secondary structures for neuropterid rrnS and rrnL genes largely agree with those known for other insects. For the first time, a model is provided for domain I of an insect rrnL. The control region in Neuropterida, as in other insects, is fast-evolving genomic region, characterized by AT-rich motifs. CONCLUSIONS: The new genome shares many features with known neuropteran genomes but differs in its low A+T content. Comparative analysis of neuropterid mitochondrial genes showed that they experienced distinct evolutionary patterns. Both tRNA families and ribosomal RNAs show composite substitution pathways. The neuropterid mitochondrial genome is characterized by a complex evolutionary history

    - Hymenoptera Sphecidae - Fauna d'Italia

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    This book is devoted to the aculeate hymenopterans belonging to the family Sphecidae (sensu Bohart & Menke, 1976). The description, natural history, behaviour and geographical distribution are provided for more than 380 species, currently recorded for the Italian Fauna. The main text is in Italian. The identification keys are provided both in Italian and English. This monograph is the 40th volume of the ongoing series Fauna of Italy published under the supervision of the Italian Academy of Entomology and the Italian Union of Zoology

    Extensive gene order rearrangement in the mitochondrial genome of the centipede Scutigera coleoptrata

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    We describe the complete mitochondrial genome of the house centipede Scutigera coleoptrata. Its gene order is unique among characterized arthropod mitochondrial genomes. Comparison to the gene order in the horseshoe crab mtDNA implies 10 or more translocations. By extending comparisons to 30 arthropod mitochondrial genomes plus two outgroups, we identify two different patterns of gene order change. The first, only affecting position and orientation of tRNAs, is much more frequent than the second, which also involves protein encoding and ribosomal genes. The analysis of the same data set using available algorithms for phylogenetic reconstruction based on gene order results in unreliable trees. This indicates that the current methods for analyzing gene order rearrangement are not suitable for wide-ranging phylogenetic studies

    The mitochondrial genome of the house centipede Scutigera and the monophyly versus paraphyly of myriapods

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    Recent advances in molecular phylogenetics are continuously changing our perception of the phylogenetic relationships among the main arthropod lineages: crustaceans, hexapods, chelicerates, and myriapods. Besides the intrinsic interest in unraveling the evolution of the largest animal phylum, these studies are basic to an understanding of one of the major transitions in animal evolution-i.e., the conquest of land with all its associated structural and functional adaptations. Myriapods have been traditionally considered the closest relatives of hexapods, thus implying only one origin of terrestriality for the tracheate lineage, but this view is now challenged by molecular evidence. Sequence data available to date for centipedes and millipedes are very limited, and the taxon sampling is strongly biased. The most critical gap was the scutigeromorph centipedes, which are the sister group to all remaining Chilopoda from which they probably diverged in the Silurian if not earlier. We obtained the first complete mitochondrial sequence for a representative of this clade, the house centipede. In our phylogenetic analyses of the protein-coding genes in this mitochondrial genome, along with 16 further ones representing the other major arthropod clades plus two outgroups, the myriapods formed a clade with the chelicerates. This implies that water-to-land transition occurred at least three times (hexapods, myriapods, arachnids) during the evolution of the Arthropoda. In addition, in contrast to all previous studies, our best supported topologies favor paraphyly of the myriapods with respect to the chelicerates. This would increase to four the main events of land colonization in arthropods (once for centipedes, once for millipedes)

    The allergenic protein Tha p 2 of processionary moths of the genus Thaumetopoea (Thaumetopoeinae, Notodontidae, Lepidoptera): Characterization and evolution

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    Abstract The allergenic Tha p 2 protein has been extracted recently from the urticating setae of the pine processionary moth Thaumetopoea pityocampa. In the present paper, we test for the occurrence of this protein in other Thaumetopoeinae, with a particular focus on members of the genus Thaumetopoea, as well as unrelated moth species, to better understand the physicochemical properties of the protein, the nature of encoding genes and their evolutionary history. Tha p 2 is encoded by the intronless gene Tha p 2 that is restricted to the processionary moths (Thaumetopoeinae, Notodontidae, Lepidoptera). Most of the species present two isoforms of Tha p 2 that can be interpreted as the result of heterozygosity in the single gene. The only exception is represented by Thaumetopoea willrinsoni, in which 20 different isoforms occur in a single specimen, leading to the conclusion that, at least in this species, multiple copies of Tha p 2 exist. Serine, glycine, cysteine and leucine are abundant in Tha p 2, a protein well conserved among processionary moths. The predicted secondary structures of Tha p 2 indicate the presence of 3 alpha-helices and six beta-barrels. Finally, the evolution of the gene and the protein was characterized by a combination of positive and negative selection, with the latter being more evident. (C) 2015 Elsevier B.V. All rights reserved

    Reconstructing animal phylogeny in the light of evolutionary developmental biology

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    The relevance of evolutionary developmental biology (evo-devo) in our effort to reconstruct the tree of life has been very poorly explored until recently. However, the contribution of an evo-devo approach to the main steps of phylogenetic analysis, such as evaluation of homology, selection of characters and assessment of character polarity can be critically important, especially in species-rich groups. As independence of traits is a prerequisite for the use of coded information in the reconstruction of phylogeny, the identification of developmentally independent units is one of the areas where evo-devo biology may offer an especially important contribution. The way in which characters originate and change in evolution has fundamental consequences on the patterns of evolutionary change we can reconstruct from character distribution. The remoulding of pre-existing features, genetic networks, or developmental trajectories, can operate at any level of biological organisation. Comparative developmental biology supports a view that homology cannot be a relationship of the all-or-nothing kind

    Aplanochytrium stocchinoi a new Labyrinthulomycota from the Southern Ocean (Ross Sea, Antarctica)

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    Aplanochytrium stocchinoi, a new species of Labyrinthulomycota, is described from samples collected in Antarctica. Ultrastructural, life cycle and molecular data characterizing the new taxon are provided and compared with the features of other species included in the genus Aplanochytrium. The phylogenetic position of A. stocchinoi is investigated using the 18S rDNA as molecular marker and applying maximum parsimony, minimum evolution and maximum likelihood methods
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