Myxozoa in Haeckel's Shadow
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FGF Signaling in Gastrulation and Neural Development in Nematostella Vectensis, an Anthozoan Cnidarian
Dev Genes Evol DOI 10.1007/s00427-006-0122-3 ORIGINAL ARTICLE FGF signaling in gastrulation and neural development in Nematostella vectensis, an anthozoan cnidarian David Q. Matus & Gerald H. Thomsen & Mark Q. Martindale Received: 8 June 2006 /Accepted: 3 November 2006 # Springer-Verlag 2007 Abstract The fibroblast growth factor (FGF) signal trans- planula stages known as the apical tuft. These results duction pathway serves as one of the key regulators of early suggest a conserved role for FGF signaling molecules in metazoan development, displaying conserved roles in the coordinating both gastrulation and neural induction that specification of endodermal, mesodermal, and neural fates predates the Cambrian explosion and the origins of the during vertebrate development. FGF signals also regulate Bilateria. gastrulation, in part, by triggering epithelial to mesenchy- mal transitions in embryos of both vertebrates and Keywords Gastrulation . Neurogenesis . invertebrates. Thus, FGF signals coordinate gastrulation Evolution of development movements across many different phyla. To help under- stand the breadth of FGF signaling deployment across the animal kingdom, we have examined the presence and Introduction expression of genes encoding FGF pathway components in the anthozoan cnidarian Nematostella vectensis. We isolat- Fibroblast growth factors (FGFs) were originally isolated ed three FGF ligands (NvFGF8A, NvFGF8B,and from vertebrate brain and pituitary fibroblasts for their roles NvFGF1A), two FGF receptors (NvFGFRa and NvFGFRb), in angiogenesis, mitogenesis, cellular differentiation, mi- and two orthologs of vertebrate FGF responsive genes, gration, and tissue-injury repair (Itoh and Ornitz 2004; Sprouty (NvSprouty), an inhibitor of FGF signaling, and Ornitz and Itoh 2001; Popovici et al. 2005). FGFs signal Churchill (NvChurchill), a Zn finger transcription factor. -
I FLATWORM PREDATION on JUVENILE FRESHWATER
FLATWORM PREDATION ON JUVENILE FRESHWATER MUSSELS A Thesis Presented to the Graduate College of Southwest Missouri State University In Partial Fulfillment of the Requirements for the Master of Science Degree By Angela Marie Delp July 2002 i FLATWORM PREDATION OF JUVENILE FRESHWATER MUSSELS Biology Department Southwest Missouri State University, July 27, 2002 Master of Science in Biology Angela Marie Delp ABSTRACT Free-living flatworms (Phylum Platyhelminthes, Class Turbellaria) are important predators on small aquatic invertebrates. Macrostomum tuba, a predominantly benthic species, feeds on juvenile freshwater mussels in fish hatcheries and mussel culture facilities. Laboratory experiments were performed to assess the predation rate of M. tuba on newly transformed juveniles of plain pocketbook mussel, Lampsilis cardium. Predation rate at 20 oC in dishes without substrate was 0.26 mussels·worm-1·h-1. Predation rate increased to 0.43 mussels·worm-1·h-1 when a substrate, polyurethane foam, was present. Substrate may have altered behavior of the predator and brought the flatworms in contact with the mussels more often. An alternative prey, the cladoceran Ceriodaphnia reticulata, was eaten at a higher rate than mussels when only one prey type was present, but at a similar rate when both were present. Finally, the effect of flatworm size (0.7- 2.2 mm long) on predation rate on mussels (0.2 mm) was tested. Predation rate increased with predator size. The slope of this relationship decreased with increasing predator size. Predation rate was near zero in 0.7 mm worms. Juvenile mussels grow rapidly and can escape flatworm predation by exceeding the size of these tiny predators. -
Cannabis Dictionary
A MEDICAL DICTIONARY, BIBLIOGRAPHY, AND ANNOTATED RESEARCH GUIDE TO INTERNET REFERENCES JAMES N. PARKER, M.D. AND PHILIP M. PARKER, PH.D., EDITORS ii ICON Health Publications ICON Group International, Inc. 4370 La Jolla Village Drive, 4th Floor San Diego, CA 92122 USA Copyright 2003 by ICON Group International, Inc. Copyright 2003 by ICON Group International, Inc. All rights reserved. This book is protected by copyright. No part of it may be reproduced, stored in a retrieval system, or transmitted in any form or by any means, electronic, mechanical, photocopying, recording, or otherwise, without written permission from the publisher. Printed in the United States of America. Last digit indicates print number: 10 9 8 7 6 4 5 3 2 1 Publisher, Health Care: Philip Parker, Ph.D. Editor(s): James Parker, M.D., Philip Parker, Ph.D. Publisher's note: The ideas, procedures, and suggestions contained in this book are not intended for the diagnosis or treatment of a health problem. As new medical or scientific information becomes available from academic and clinical research, recommended treatments and drug therapies may undergo changes. The authors, editors, and publisher have attempted to make the information in this book up to date and accurate in accord with accepted standards at the time of publication. The authors, editors, and publisher are not responsible for errors or omissions or for consequences from application of the book, and make no warranty, expressed or implied, in regard to the contents of this book. Any practice described in this book should be applied by the reader in accordance with professional standards of care used in regard to the unique circumstances that may apply in each situation. -
Cumulated Bibliography of Biographies of Ocean Scientists Deborah Day, Scripps Institution of Oceanography Archives Revised December 3, 2001
Cumulated Bibliography of Biographies of Ocean Scientists Deborah Day, Scripps Institution of Oceanography Archives Revised December 3, 2001. Preface This bibliography attempts to list all substantial autobiographies, biographies, festschrifts and obituaries of prominent oceanographers, marine biologists, fisheries scientists, and other scientists who worked in the marine environment published in journals and books after 1922, the publication date of Herdman’s Founders of Oceanography. The bibliography does not include newspaper obituaries, government documents, or citations to brief entries in general biographical sources. Items are listed alphabetically by author, and then chronologically by date of publication under a legend that includes the full name of the individual, his/her date of birth in European style(day, month in roman numeral, year), followed by his/her place of birth, then his date of death and place of death. Entries are in author-editor style following the Chicago Manual of Style (Chicago and London: University of Chicago Press, 14th ed., 1993). Citations are annotated to list the language if it is not obvious from the text. Annotations will also indicate if the citation includes a list of the scientist’s papers, if there is a relationship between the author of the citation and the scientist, or if the citation is written for a particular audience. This bibliography of biographies of scientists of the sea is based on Jacqueline Carpine-Lancre’s bibliography of biographies first published annually beginning with issue 4 of the History of Oceanography Newsletter (September 1992). It was supplemented by a bibliography maintained by Eric L. Mills and citations in the biographical files of the Archives of the Scripps Institution of Oceanography, UCSD. -
Ctenophore Relationships and Their Placement As the Sister Group to All Other Animals
ARTICLES DOI: 10.1038/s41559-017-0331-3 Ctenophore relationships and their placement as the sister group to all other animals Nathan V. Whelan 1,2*, Kevin M. Kocot3, Tatiana P. Moroz4, Krishanu Mukherjee4, Peter Williams4, Gustav Paulay5, Leonid L. Moroz 4,6* and Kenneth M. Halanych 1* Ctenophora, comprising approximately 200 described species, is an important lineage for understanding metazoan evolution and is of great ecological and economic importance. Ctenophore diversity includes species with unique colloblasts used for prey capture, smooth and striated muscles, benthic and pelagic lifestyles, and locomotion with ciliated paddles or muscular propul- sion. However, the ancestral states of traits are debated and relationships among many lineages are unresolved. Here, using 27 newly sequenced ctenophore transcriptomes, publicly available data and methods to control systematic error, we establish the placement of Ctenophora as the sister group to all other animals and refine the phylogenetic relationships within ctenophores. Molecular clock analyses suggest modern ctenophore diversity originated approximately 350 million years ago ± 88 million years, conflicting with previous hypotheses, which suggest it originated approximately 65 million years ago. We recover Euplokamis dunlapae—a species with striated muscles—as the sister lineage to other sampled ctenophores. Ancestral state reconstruction shows that the most recent common ancestor of extant ctenophores was pelagic, possessed tentacles, was bio- luminescent and did not have separate sexes. Our results imply at least two transitions from a pelagic to benthic lifestyle within Ctenophora, suggesting that such transitions were more common in animal diversification than previously thought. tenophores, or comb jellies, have successfully colonized from species across most of the known phylogenetic diversity of nearly every marine environment and can be key species in Ctenophora. -
Cephalopodologie
Reprint Series W /~»T ¥7 "IVT^l? 18 May 1990, Volume 248, pp. 898-899 OvJ-lLllL/EJ Cephalopodologie CLYDE F. E. ROPER Copyright © 1990 by the American Association for the Advancement of Science Cephalopodologie work to be outdated, Portmann abandoned the notes and wrote a 200-page manuscript, which he submitted in 1954. Because the Traits de Zoologie. Anatomic, Systcmatique, recendy submitted gastropod and bivalve Biologic. PIERRE P. GRASSE, Ed. Tome 5, fasci- manuscripts ran to 4600 pages, Grasse re- cule 4, Cephalopodes. KATHARINA. MANGOLD, quired that the cephalopod section be in- Ed. Masson, Paris, 1989. 804 pp. F1100. creased to 400, a task the displeased Port- Comprehensive reference works frequent- mann was unwilling to undertake until the ly require a number of years to compile, are early 1960s. The resurgence of research on eagerly awaited by specialists, and once pub- cephalopods then prompted Portmann to lished gradually come into general use by enlist Katharina Mangold, a former student researchers, educators, and students. The and established cephalopod specialist at La- volumes of The Invertebrates inaugurated by boratoire Arago, Banyuls-sur-Mer, France, Libbie Hyman in 1940 provide an excellent to incorporate the new literature into the example of such a history, as does the classic manuscript. By the time one section was Traite de Zoologie directed by Pierre P. updated, preceding ones had become obso- Grasse. lete, and, as the objective of the Traite was to Among works of such lengthy gestation be "comprehensive," the project became the present installment of the Traite surely locked in a cycle of updates. -
Cadherin Switch Marks Germ Layer Formation in the Diploblastic Sea Anemone Nematostella Vectensis
bioRxiv preprint doi: https://doi.org/10.1101/488270; this version posted December 6, 2018. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. Cadherin switch marks germ layer formation in the diploblastic sea anemone Nematostella vectensis PUKHLYAKOVA, E.A.1, KIRILLOVA, A.1,2, KRAUS, Y.A. 2, TECHNAU, U.1 1 Department for Molecular Evolution and Development, Centre of Organismal Systems Biology, University of Vienna, Althanstraße 14, A-1090 Vienna, Austria. 2 Department of Evolutionary Biology, Biological Faculty, Moscow State University, Leninskie Gory 1/12, 119991, Moscow, Russia. Key words: cadherin, cell adhesion, morphogenesis, germ layers, Nematostella, Cnidaria Abstract Morphogenesis is a shape-building process during development of multicellular organisms. During this process the establishment and modulation of cell-cell contacts play an important role. Cadherins, the major cell adhesion molecules, form adherens junctions connecting ephithelial cells. Numerous studies in Bilateria have shown that cadherins are associated with the regulation of cell differentiation, cell shape changes, cell migration and tissue morphogenesis. To date, the role of Cadherins in non- bilaterians is unknown. Here, we study the expression and the function of two paralogous classical cadherins, cadherin1 and cadherin3, in the diploblastic animal, the sea anemone Nematostella vectensis. We show that a cadherin switch is accompanying the formation of germ layers. Using specific antibodies, we show that both cadherins are localized to adherens junctions at apical and basal positions in ectoderm and endoderm. -
University of Copenhagen, Zoological Museum, Review Universitetsparken 15, DK-2100 Copenhagen, Denmark CN, 0000-0001-6898-7655 Cite This Article: Nielsen C
Early animal evolution a morphologist's view Nielsen, Claus Published in: Royal Society Open Science DOI: 10.1098/rsos.190638 Publication date: 2019 Document version Publisher's PDF, also known as Version of record Document license: CC BY Citation for published version (APA): Nielsen, C. (2019). Early animal evolution: a morphologist's view. Royal Society Open Science, 6(7), 1-10. [190638]. https://doi.org/10.1098/rsos.190638 Download date: 30. sep.. 2021 Early animal evolution: a morphologist’s view royalsocietypublishing.org/journal/rsos Claus Nielsen The Natural History Museum of Denmark, University of Copenhagen, Zoological Museum, Review Universitetsparken 15, DK-2100 Copenhagen, Denmark CN, 0000-0001-6898-7655 Cite this article: Nielsen C. 2019 Early animal evolution: a morphologist’s view. R. Soc. open sci. Two hypotheses for the early radiation of the metazoans are vividly discussed in recent phylogenomic studies, the ‘Porifera- 6: 190638. first’ hypothesis, which places the poriferans as the sister group http://dx.doi.org/10.1098/rsos.190638 of all other metazoans, and the ‘Ctenophora-first’ hypothesis, which places the ctenophores as the sister group to all other metazoans. It has been suggested that an analysis of morphological characters (including specific molecules) could Received: 5 April 2019 throw additional light on the controversy, and this is the aim of Accepted: 4 July 2019 this paper. Both hypotheses imply independent evolution of nervous systems in Planulozoa and Ctenophora. The Porifera- first hypothesis implies no homoplasies or losses of major characters. The Ctenophora-first hypothesis shows no important synapomorphies of Porifera, Planulozoa and Placozoa. It implies Subject Category: either independent evolution, in Planulozoa and Ctenophora, of Biology (whole organism) a new digestive system with a gut with extracellular digestion, which enables feeding on larger organisms, or the subsequent Subject Areas: loss of this new gut in the Poriferans (and the re-evolution of the evolution collar complex). -
Toxin-Like Neuropeptides in the Sea Anemone Nematostella Unravel Recruitment from the Nervous System to Venom
Toxin-like neuropeptides in the sea anemone Nematostella unravel recruitment from the nervous system to venom Maria Y. Sachkovaa,b,1, Morani Landaua,2, Joachim M. Surma,2, Jason Macranderc,d, Shir A. Singera, Adam M. Reitzelc, and Yehu Morana,1 aDepartment of Ecology, Evolution, and Behavior, Alexander Silberman Institute of Life Sciences, Faculty of Science, Hebrew University of Jerusalem, 9190401 Jerusalem, Israel; bSars International Centre for Marine Molecular Biology, University of Bergen, 5007 Bergen, Norway; cDepartment of Biological Sciences, University of North Carolina at Charlotte, Charlotte, NC 28223; and dBiology Department, Florida Southern College, Lakeland, FL 33801 Edited by Baldomero M. Olivera, University of Utah, Salt Lake City, UT, and approved September 14, 2020 (received for review May 31, 2020) The sea anemone Nematostella vectensis (Anthozoa, Cnidaria) is a to a target receptor in the nervous system of the prey or predator powerful model for characterizing the evolution of genes func- interfering with transmission of electric impulses. For example, tioning in venom and nervous systems. Although venom has Nv1 toxin from Nematostella inhibits inactivation of arthropod evolved independently numerous times in animals, the evolution- sodium channels (12), while ShK toxin from Stichodactyla heli- ary origin of many toxins remains unknown. In this work, we pin- anthus is a potassium channel blocker (13). Nematostella’snem- point an ancestral gene giving rise to a new toxin and functionally atocytes produce multiple toxins with a 6-cysteine pattern of the characterize both genes in the same species. Thus, we report a ShK toxin (7, 9). The ShKT superfamily is ubiquitous across sea case of protein recruitment from the cnidarian nervous to venom anemones (14); however, its evolutionary origin remains unknown. -
Sak/Plk4 and Mitotic Fidelity
Oncogene (2005) 24, 306–312 & 2005 Nature Publishing Group All rights reserved 0950-9232/05 $30.00 www.nature.com/onc Sak/Plk4 and mitotic fidelity Carol J Swallow1,2, Michael A Ko1,2, Najeeb U Siddiqui1,3,4, John W Hudson5 and James W Dennis*,1,3,4 1Samuel Lunenfeld Research Institute, Mount Sinai Hospital, 600 University Ave. R988, Toronto, Ontario, Canada M5G 1X5; 2Department of Surgery, University of Toronto, Ontario, Canada; 3Department of Microbiology and Medical Genetics, University of Toronto, Ontario, Canada; 4Department of Laboratory Medicine and Pathobiology, University of Toronto, Ontario, Canada; 5Department of Biological Sciences, University of Windsor, Ontario, Canada Sak/Plk4 differs from other polo-like kinases in having (Fernebro et al., 2002). Mutation of classical tumor only a single polo box, which assumes a novel dimer fold suppressor genes follows the Knudsen 2-hit model, that localizes to the nucleolus, centrosomes and the whereby loss of the wild-type allele as a ‘second hit’ cleavage furrow.Sak expression increases gradually in S frequently results in relaxed cellular growth controls through M phase, and Sak is destroyed by APC/C (Knudson, 1971). Inherited cancer syndromes such as dependent proteolysis.Sak-deficient mouse embryos Li-Fraumeni (p53, Chk2) and ataxia telangiectasia arrest at E7.5 and display an increased incidence of (ATM) are examples of autosomal recessive mutations apoptosis and anaphase arrest.Sak þ /À mice are haploin- in checkpoint proteins that normally delay the cell cycle sufficient for tumor suppression, with spontaneous tumors in response to DNA damage and environmental stresses developing primarily in the liver with advanced age. -
Feeding-Dependent Tentacle Development in the Sea Anemone Nematostella Vectensis ✉ Aissam Ikmi 1,2 , Petrus J
ARTICLE https://doi.org/10.1038/s41467-020-18133-0 OPEN Feeding-dependent tentacle development in the sea anemone Nematostella vectensis ✉ Aissam Ikmi 1,2 , Petrus J. Steenbergen1, Marie Anzo 1, Mason R. McMullen2,3, Anniek Stokkermans1, Lacey R. Ellington2 & Matthew C. Gibson2,4 In cnidarians, axial patterning is not restricted to embryogenesis but continues throughout a prolonged life history filled with unpredictable environmental changes. How this develop- 1234567890():,; mental capacity copes with fluctuations of food availability and whether it recapitulates embryonic mechanisms remain poorly understood. Here we utilize the tentacles of the sea anemone Nematostella vectensis as an experimental paradigm for developmental patterning across distinct life history stages. By analyzing over 1000 growing polyps, we find that tentacle progression is stereotyped and occurs in a feeding-dependent manner. Using a combination of genetic, cellular and molecular approaches, we demonstrate that the crosstalk between Target of Rapamycin (TOR) and Fibroblast growth factor receptor b (Fgfrb) signaling in ring muscles defines tentacle primordia in fed polyps. Interestingly, Fgfrb-dependent polarized growth is observed in polyp but not embryonic tentacle primordia. These findings show an unexpected plasticity of tentacle development, and link post-embryonic body patterning with food availability. 1 Developmental Biology Unit, European Molecular Biology Laboratory, 69117 Heidelberg, Germany. 2 Stowers Institute for Medical Research, Kansas City, MO 64110, -
Animal Phylum Poster Porifera
Phylum PORIFERA CNIDARIA PLATYHELMINTHES ANNELIDA MOLLUSCA ECHINODERMATA ARTHROPODA CHORDATA Hexactinellida -- glass (siliceous) Anthozoa -- corals and sea Turbellaria -- free-living or symbiotic Polychaetes -- segmented Gastopods -- snails and slugs Asteroidea -- starfish Trilobitomorpha -- tribolites (extinct) Urochordata -- tunicates Groups sponges anemones flatworms (Dugusia) bristleworms Bivalves -- clams, scallops, mussels Echinoidea -- sea urchins, sand Chelicerata Cephalochordata -- lancelets (organisms studied in detail in Demospongia -- spongin or Hydrazoa -- hydras, some corals Trematoda -- flukes (parasitic) Oligochaetes -- earthworms (Lumbricus) Cephalopods -- squid, octopus, dollars Arachnida -- spiders, scorpions Mixini -- hagfish siliceous sponges Xiphosura -- horseshoe crabs Bio1AL are underlined) Cubozoa -- box jellyfish, sea wasps Cestoda -- tapeworms (parasitic) Hirudinea -- leeches nautilus Holothuroidea -- sea cucumbers Petromyzontida -- lamprey Mandibulata Calcarea -- calcareous sponges Scyphozoa -- jellyfish, sea nettles Monogenea -- parasitic flatworms Polyplacophora -- chitons Ophiuroidea -- brittle stars Chondrichtyes -- sharks, skates Crustacea -- crustaceans (shrimp, crayfish Scleropongiae -- coralline or Crinoidea -- sea lily, feather stars Actinipterygia -- ray-finned fish tropical reef sponges Hexapoda -- insects (cockroach, fruit fly) Sarcopterygia -- lobed-finned fish Myriapoda Amphibia (frog, newt) Chilopoda -- centipedes Diplopoda -- millipedes Reptilia (snake, turtle) Aves (chicken, hummingbird) Mammalia