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1. A Caenorhabditis elegans Model for Integrating the Functions of Neuropsychiatric Risk Genes Identifies Components Required for Normal Dendritic Morphology

Author

Cristina Aguirre-Chen, Natalia Stec, Olivia Mendivil Ramos, Nuri Kim, Melissa Kramer, Shane McCarthy, Jesse Gillis, W. Richard McCombie, and Christopher M. Hammell

Subjects
caenorhabditis elegans, autism spectrum disorder, schizophrenia, neuropsychiatric risk genes, rna interference, dendritic arborization, model organism, neuronal development, Genetics, QH426-470
Abstract

Analysis of patient-derived DNA samples has identified hundreds of variants that are likely involved in neuropsychiatric diseases such as autism spectrum disorder (ASD) and schizophrenia (SCZ). While these studies couple behavioral phenotypes to individual genotypes, the number and diversity of candidate genes implicated in these disorders highlights the fact that the mechanistic underpinnings of these disorders are largely unknown. Here, we describe a RNAi-based screening platform that uses C. elegans to screen candidate neuropsychiatric risk genes (NRGs) for roles in controlling dendritic arborization. To benchmark this approach, we queried published lists of NRGs whose variants in ASD and SCZ are predicted to result in complete or partial loss of gene function. We found that a significant fraction (>16%) of these candidate NRGs are essential for dendritic development. Furthermore, these gene sets are enriched for dendritic arbor phenotypes (>14 fold) when compared to control RNAi datasets of over 500 human orthologs. The diversity of PVD structural abnormalities observed in these assays suggests that the functions of diverse NRGs (encoding transcription factors, chromatin remodelers, molecular chaperones and cytoskeleton-related proteins) converge to regulate neuronal morphology and that individual NRGs may play distinct roles in dendritic branching. We also demonstrate that the experimental value of this platform by providing additional insights into the molecular frameworks of candidate NRGs. Specifically, we show that ANK2/UNC-44 function is directly integrated with known regulators of dendritic arborization and suggest that altering the dosage of ARID1B/LET-526 expression during development affects neuronal morphology without diminishing aspects of cell fate specification.

Published
2020
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2. The first myriapod genome sequence reveals conservative arthropod gene content and genome organisation in the centipede Strigamia maritima.

Author

Ariel D Chipman, David E K Ferrier, Carlo Brena, Jiaxin Qu, Daniel S T Hughes, Reinhard Schröder, Montserrat Torres-Oliva, Nadia Znassi, Huaiyang Jiang, Francisca C Almeida, Claudio R Alonso, Zivkos Apostolou, Peshtewani Aqrawi, Wallace Arthur, Jennifer C J Barna, Kerstin P Blankenburg, Daniela Brites, Salvador Capella-Gutiérrez, Marcus Coyle, Peter K Dearden, Louis Du Pasquier, Elizabeth J Duncan, Dieter Ebert, Cornelius Eibner, Galina Erikson, Peter D Evans, Cassandra G Extavour, Liezl Francisco, Toni Gabaldón, William J Gillis, Elizabeth A Goodwin-Horn, Jack E Green, Sam Griffiths-Jones, Cornelis J P Grimmelikhuijzen, Sai Gubbala, Roderic Guigó, Yi Han, Frank Hauser, Paul Havlak, Luke Hayden, Sophie Helbing, Michael Holder, Jerome H L Hui, Julia P Hunn, Vera S Hunnekuhl, LaRonda Jackson, Mehwish Javaid, Shalini N Jhangiani, Francis M Jiggins, Tamsin E Jones, Tobias S Kaiser, Divya Kalra, Nathan J Kenny, Viktoriya Korchina, Christie L Kovar, F Bernhard Kraus, François Lapraz, Sandra L Lee, Jie Lv, Christigale Mandapat, Gerard Manning, Marco Mariotti, Robert Mata, Tittu Mathew, Tobias Neumann, Irene Newsham, Dinh N Ngo, Maria Ninova, Geoffrey Okwuonu, Fiona Ongeri, William J Palmer, Shobha Patil, Pedro Patraquim, Christopher Pham, Ling-Ling Pu, Nicholas H Putman, Catherine Rabouille, Olivia Mendivil Ramos, Adelaide C Rhodes, Helen E Robertson, Hugh M Robertson, Matthew Ronshaugen, Julio Rozas, Nehad Saada, Alejandro Sánchez-Gracia, Steven E Scherer, Andrew M Schurko, Kenneth W Siggens, DeNard Simmons, Anna Stief, Eckart Stolle, Maximilian J Telford, Kristin Tessmar-Raible, Rebecca Thornton, Maurijn van der Zee, Arndt von Haeseler, James M Williams, Judith H Willis, Yuanqing Wu, Xiaoyan Zou, Daniel Lawson, Donna M Muzny, Kim C Worley, Richard A Gibbs, Michael Akam, and Stephen Richards

Subjects
Biology (General), QH301-705.5
Abstract

Myriapods (e.g., centipedes and millipedes) display a simple homonomous body plan relative to other arthropods. All members of the class are terrestrial, but they attained terrestriality independently of insects. Myriapoda is the only arthropod class not represented by a sequenced genome. We present an analysis of the genome of the centipede Strigamia maritima. It retains a compact genome that has undergone less gene loss and shuffling than previously sequenced arthropods, and many orthologues of genes conserved from the bilaterian ancestor that have been lost in insects. Our analysis locates many genes in conserved macro-synteny contexts, and many small-scale examples of gene clustering. We describe several examples where S. maritima shows different solutions from insects to similar problems. The insect olfactory receptor gene family is absent from S. maritima, and olfaction in air is likely effected by expansion of other receptor gene families. For some genes S. maritima has evolved paralogues to generate coding sequence diversity, where insects use alternate splicing. This is most striking for the Dscam gene, which in Drosophila generates more than 100,000 alternate splice forms, but in S. maritima is encoded by over 100 paralogues. We see an intriguing linkage between the absence of any known photosensory proteins in a blind organism and the additional absence of canonical circadian clock genes. The phylogenetic position of myriapods allows us to identify where in arthropod phylogeny several particular molecular mechanisms and traits emerged. For example, we conclude that juvenile hormone signalling evolved with the emergence of the exoskeleton in the arthropods and that RR-1 containing cuticle proteins evolved in the lineage leading to Mandibulata. We also identify when various gene expansions and losses occurred. The genome of S. maritima offers us a unique glimpse into the ancestral arthropod genome, while also displaying many adaptations to its specific life history.

Published
2014
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3. A Caenorhabditis elegans Model for Integrating the Functions of Neuropsychiatric Risk Genes Identifies Components Required for Normal Dendritic Morphology

Author

W. Richard McCombie, Christopher M. Hammell, Melissa Kramer, Natalia Stec, Jesse Gillis, Olivia Mendivil Ramos, Nuri Kim, Shane McCarthy, and Cristina Aguirre-Chen

Subjects
Candidate gene, ved/biology.organism_classification_rank.species, autism spectrum disorder, Computational biology, Cell fate determination, QH426-470, rna interference, 03 medical and health sciences, 0302 clinical medicine, RNA interference, neuronal development, Genetics, Model organism, Molecular Biology, Transcription factor, model organism, Genetics (clinical), Caenorhabditis elegans, 030304 developmental biology, 0303 health sciences, biology, ved/biology, neuropsychiatric risk genes, biology.organism_classification, Phenotype, Chromatin, schizophrenia, caenorhabditis elegans, dendritic arborization, 030217 neurology & neurosurgery
Abstract

Analysis of patient-derived DNA samples has identified hundreds of variants that are likely involved in neuropsychiatric diseases such as autism spectrum disorder (ASD) and schizophrenia (SCZ). While these studies couple behavioral phenotypes to individual genotypes, the number and diversity of candidate genes implicated in these disorders highlights the fact that the mechanistic underpinnings of these disorders are largely unknown. Here, we describe a RNAi-based screening platform that uses C. elegans to screen candidate neuropsychiatric risk genes (NRGs) for roles in controlling dendritic arborization. To benchmark this approach, we queried published lists of NRGs whose variants in ASD and SCZ are predicted to result in complete or partial loss of gene function. We found that a significant fraction (>16%) of these candidate NRGs are essential for dendritic development. Furthermore, these gene sets are enriched for dendritic arbor phenotypes (>14 fold) when compared to control RNAi datasets of over 500 human orthologs. The diversity of PVD structural abnormalities observed in these assays suggests that the functions of diverse NRGs (encoding transcription factors, chromatin remodelers, molecular chaperones and cytoskeleton-related proteins) converge to regulate neuronal morphology and that individual NRGs may play distinct roles in dendritic branching. We also demonstrate that the experimental value of this platform by providing additional insights into the molecular frameworks of candidate NRGs. Specifically, we show that ANK2/UNC-44 function is directly integrated with known regulators of dendritic arborization and suggest that altering the dosage of ARID1B/LET-526 expression during development affects neuronal morphology without diminishing aspects of cell fate specification.

Published
2020

4. Long-read sequencing reveals rapid evolution of immunity- and cancer-related genes in bats

Author

W. Richard McCombie, Daniel J. Becker, Sara Goodwin, Sara J. Oppenheim, Olivia Mendivil Ramos, Nancy B. Simmons, Michael C. Schatz, Melissa Kramer, Armin Scheben, and Adam Siepel

Subjects
Most recent common ancestor, Evolutionary biology, Gene duplication, Pteronotus, Gene family, Locus (genetics), Biology, biology.organism_classification, Gene, Genome, Artibeus
Abstract

Bats are exceptional among mammals for their powered flight, extended lifespans, and robust immune systems. To investigate the genomic underpinnings of unique bat adaptations, we sequenced the genomes of the Jamaican fruit bat (Artibeus jamaicensis) and the Mesoamerican mustached bat (Pteronotus mesoamericanus) and compared them to a diverse collection of 13 additional bat species together with other mammals. We used the Oxford Nanopore Technologies long-read platform to generate highly complete assemblies (N50: 28-29Mb) and facilitate analysis of complex genomic regions containing duplicated genes. Using gene family size analysis, we found that the type I interferon locus was contracted by eight genes in the most recent common ancestor (MRCA) of bats, shifting the proportion of interferon-ω to interferon-α and making interferon-ω the most common type I interferon in bats. Antiviral genes stimulated by type I interferons were also rapidly evolving, with interferon-induced transmembrane genes experiencing a lineage-specific duplication and strong positive selection in the gene IFIT2. Moreover, the lineage of phyllostomid bats showed an unprecedented expansion of PRDM9, a recombination-related gene also involved in infection responses, raising the possibility that this gene contributes to bat antiviral defenses. These modifications in the bat innate immune system may be important adaptations allowing them to harbor viruses asymptomatically. We additionally found evidence of positive selection on the branch leading to the MRCA of bats acting on 33 tumor suppressors and six DNA repair genes, which may contribute to the low cancer rates and longevity observed across bats. These new genomic resources enable insights into the extraordinary adaptations of bats, with implications for mammalian evolutionary studies and public health.

Published
2020

5. A

Author

Cristina, Aguirre-Chen, Natalia, Stec, Olivia Mendivil, Ramos, Nuri, Kim, Melissa, Kramer, Shane, McCarthy, Jesse, Gillis, W Richard, McCombie, and Christopher M, Hammell

Subjects
schizophrenia, RNA interference, Autism Spectrum Disorder, neuronal development, Animals, Humans, neuropsychiatric risk genes, Investigations, Caenorhabditis elegans, Caenorhabditis elegans Proteins, dendritic arborization, model organism, Transcription Factors
Abstract

Analysis of patient-derived DNA samples has identified hundreds of variants that are likely involved in neuropsychiatric diseases such as autism spectrum disorder (ASD) and schizophrenia (SCZ). While these studies couple behavioral phenotypes to individual genotypes, the number and diversity of candidate genes implicated in these disorders highlights the fact that the mechanistic underpinnings of these disorders are largely unknown. Here, we describe a RNAi-based screening platform that uses C. elegans to screen candidate neuropsychiatric risk genes (NRGs) for roles in controlling dendritic arborization. To benchmark this approach, we queried published lists of NRGs whose variants in ASD and SCZ are predicted to result in complete or partial loss of gene function. We found that a significant fraction (>16%) of these candidate NRGs are essential for dendritic development. Furthermore, these gene sets are enriched for dendritic arbor phenotypes (>14 fold) when compared to control RNAi datasets of over 500 human orthologs. The diversity of PVD structural abnormalities observed in these assays suggests that the functions of diverse NRGs (encoding transcription factors, chromatin remodelers, molecular chaperones and cytoskeleton-related proteins) converge to regulate neuronal morphology and that individual NRGs may play distinct roles in dendritic branching. We also demonstrate that the experimental value of this platform by providing additional insights into the molecular frameworks of candidate NRGs. Specifically, we show that ANK2/UNC-44 function is directly integrated with known regulators of dendritic arborization and suggest that altering the dosage of ARID1B/LET-526 expression during development affects neuronal morphology without diminishing aspects of cell fate specification.

Published
2020

6. BioTIME: A database of biodiversity time series for the Anthropocene

Author

Grace E. Frank, Alecia Bellgrove, Flaviana Maluf Souza, Fakhrizal Setiawan, Vladimir G. Onipchenko, Miguel Barbosa, J. Emmett Duffy, Robert A. Davis, Giselda Durigan, Jan Vanaverbeke, Ricardo Rocha, Ana Paula Savassi-Coutinho, Francis Neat, Emily H. Stanley, Erkki Pulliainen, Vinicius Castro Souza, Stephen F. Newton, N. A. Mil'chakova, Annika Hofgaard, James A. Nelson, Elisabeth J. Cooper, Lisandro Benedetti-Cecchi, Sonja Wipf, Anders Enemar, Gabriel Barros Gonçalves de Souza, Claire Laguionie-Marchais, Dušan Adam, Robert N. L. Fitt, Christopher P. Bloch, Claus Bässler, Gediminas Vaitkus, Magdalena Błażewicz, Robert R. Twilley, Richard Condit, B.R. Ramesh, Chaolun Allen Chen, Grace E. P. Murphy, Kevin P. Robinson, Gal Badihi, Lars G. Rudstam, J. Jonathan Moore, David M. Paterson, Sarah R. Supp, Claire E. Widdicombe, Suzanne M. Remillard, Hans M. Verheye, Jill F. Johnstone, Claire H. Davies, Shane A. Blowes, Mark E. Harmon, Rick D. Stuart-Smith, Andrew J. Brooks, Gert Van Hoey, José Eduardo Rebelo, Anna Maria Fosaa, Tim S. Doherty, Jasper A. Slingsby, Francesco Pomati, Raphaël Pélissier, Ward Appeltans, José Manuel Arcos, Phaedra Budy, Victor H. Rivera-Monroy, Maria Teresa Zugliani Toniato, Anthony J. Richardson, Luiz Fernando Loureiro Fernandes, Christopher D. Stallings, Rowan Stanforth, David J. Kushner, A. A. Akhmetzhanova, Geraldo Antônio Daher Corrêa Franco, Alessandra Fidelis, Elizabeth Gorgone-Barbosa, Dave Watts, S.A. Tarigan, Timothy C. Bonebrake, Kent P. McFarland, Jonathan Belmaker, Shahar Malamud, Kamil Král, John D. Lloyd, Diane M. McKnight, Alessandra Rocha Kortz, Luise Hermanutz, Tore Johannessen, N. Ayyappan, Brian J. Bett, Haley Arnold, Fernando Rodrigues da Silva, Peter L. Meserve, Francisco Lloret, Nadejda A. Soudzilovskaia, Michael R. Willig, Linda A. Kuhnz, Esther Lévesque, Kwang-Tsao Shao, Sofía Sal, Robert D. Hollister, Andrew Rassweiler, Christoph F. J. Meyer, Jeffrey C. Oliver, Isla H. Myers-Smith, Graham J. Edgar, Jacek Siciński, Beatriz Salgado, Fábio Venturoli, Matt Bradford, Borgþór Magnússon, Edward Castañeda-Moya, Anne D. Bjorkman, Eric Post, Alain Paquette, Or Givan, Jonathan S. Lefcheck, Falk Huettmann, Fábio Lang da Silveira, Roberto Cazzolla Gatti, Thomas J. Valone, Sarah C. Elmendorf, Sinta Pardede, Esben Moland Olsen, Laura Siegwart Collier, Flavio Antonio Maës dos Santos, Andrew H. Baird, Cheol Min Lee, Robert B. Waide, Olivia Mendivil Ramos, David C. Lightfoot, Stefan B. Williams, Ute Jandt, David Janík, Stephen S. Hale, Robin Elahi, Andrew L. Rypel, S. K. Morgan Ernest, Jörg Müller, Gaius R. Shaver, Anna Jażdżewska, José Mauro Sterza, Maarten Stevens, Denise de Cerqueira Rossa-Feres, Dor Edelist, Martha Isabel Vallejo, Michael Paul Nelson, Conor Waldock, Ricardo Ribeiro Rodrigues, Sally Sherman, Dustin J. Wilgers, Sharon K. Collinge, Kristen T. Holeck, Josep Peñuelas, Douglas A. Kelt, Tiago Egydio Barreto, Faye Moyes, Robert L. Schooley, Peter B. Reich, Jason Meador, Anders Michelsen, J. Paul Richardson, Sara J. Snell, Julio R. Gutiérrez, Chih-hao Hsieh, Gary D. Grossman, Hernando García, Ana Carolina da Silva, Kyle J. A. Zawada, Richard T. Holmes, John C. Priscu, Christine L. Huffard, Christian Rixen, William O. McLarney, Julia A. Jones, Anne Tolvanen, William A. Gould, Maite Louzao, Alejandro Pérez-Matus, Donald L. Henshaw, Kathleen L. Prudic, Herbert H. T. Prins, Helge Bruelheide, Catalina S. Ruz, Rui P. Vieira, Gary P. Thiede, Erin C. Keeley, James H. Brown, William R. Fraser, Pieter Provoost, Andrew S. Hoey, Robert J. Pabst, Kerry D. Woods, Fabiano Turini Farah, Nancy B. Rybicki, Sara E. Scanga, Trevor J. Willis, Daniel J. Metcalfe, Mark Williamson, Joshua S. Madin, Tasrif Kartawijaya, Brian J. McGill, Erica M. Sampaio, Shannan K. Crow, Stephen P. Hubbell, Jochen Schmidt, Daniel C. Reed, Steven Degraer, Laura H. Antão, Krzysztof Pabis, Christopher C. Koenig, Fernando Carvalho, Marcelo Vianna, Anne E. Magurran, Marc Estiarte, Rebecca Kinnear, Tracey Smart, Lesley T. Lancaster, Frank P. Day, Natalia Norden, Unai Cotano, Fábio Z. Farneda, Nelson Valdivia, Corinna Gries, Tomasz Wesołowski, Pedro Higuchi, Jungwon Kang, Randall W. Myster, Itai van Rijn, Oscar Pizarro, Michael L. Zettler, Simon Thorn, Thomas W. Sherry, Timothy E. Dunn, Tung-Yung Fan, Susan Boyd, Adrià López-Baucells, Tomáš Vrška, Tory J. Chase, Ruben Escribano, R. Williams, Carolina Mathias Moreira, John F. Chamblee, Con Quang Vu, Halvor Knutsen, Amanda E. Bates, Maria Dornelas, Kari Klanderud, Jorge Yoshio Tamashiro, Tom Moens, Sara L. Webb, Iain Matthews, Carl Van Colen, Chao-Yang Kuo, Caya Sievers, Faith A. M. Jones, Gary Haskins, Eric J. Woehler, J. Hans C. Cornelissen, Allen H. Hurlbert, Mia O. Hoogenboom, Pamela Hidalgo, Henry A. Ruhl, Brian S. Evans, Ørjan Totland, Lien Van Vu, Yzel Rondon Súarez, Gabriella Damasceno, Even Moland, John Harte, Andrew Naumov, Ethan P. White, Natália Macedo Ivanauskas, Systems Ecology, International Oceanographic Data and Information Exchange (IODE) of the Intergovernmental Oceanographic Commission of UNESCO, Oostende, Safety science group, Delft University of Technology (TU Delft), Institut Français de Pondichéry (IFP), Centre National de la Recherche Scientifique (CNRS)-Ministère de l'Europe et des Affaires étrangères (MEAE), Department of Biology [Pisa], University of Pisa - Università di Pisa, CSIRO Land and Water, Commonwealth Scientific and Industrial Research Organisation [Canberra] (CSIRO), Institute of Biology/Geobotany and Botanical Garden, Martin-Luther-Universität Halle Wittenberg (MLU), Management Unit of the Mathematical Model of the North Sea, Royal Belgian Insitute of Natural Sciences, Floresta Estadual Assis, Global Ecology Unit CREAF-CEAB-CSIC, Universitat Autònoma de Barcelona [Barcelona] (UAB), National Museum of Marine Biology and Aquarium, Universidade de São Paulo (USP), Polar Oceans Research Group [USA], Department of Zoology, Tel Aviv University [Tel Aviv], Norwegian Institute for Nature Research (NINA), EWHALE Laboratory of Biology and Wildlife Department, Institute of Arctic Biology-University of Alaska [Fairbanks] (UAF), Laboratory of Polar Biology and Oceanobiology, University of Lódź, Dept Ecol Evol Biol, Univ California SC (EEB-UCSC), University of California [Santa Cruz] (UCSC), University of California-University of California, Département de chimie-biologie & Centre d’études nordiques [CANADA], Université du Québec à Trois-Rivières (UQTR), Human Communication Technologies Research Laboratory (UBC), University of British Columbia (UBC), Instituto Espanol de Oceanografia, Instituto Español de Oceanografía, Department of Biology [Copenhagen], Faculty of Science [Copenhagen], University of Copenhagen = Københavns Universitet (KU)-University of Copenhagen = Københavns Universitet (KU), Institute of Marine Research, Flødevigen Marine Research Station, Computer Laboratory [Cambridge], University of Cambridge [UK] (CAM), Aarhus University [Aarhus], Evolution et Diversité Biologique (EDB), Institut de Recherche pour le Développement (IRD)-Université Toulouse III - Paul Sabatier (UT3), Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées-Centre National de la Recherche Scientifique (CNRS), Centre for Forest Research (CFR), Université du Québec à Montréal (UQAM), The Centre for Applied Genomics, Toronto, University of Toronto-The Hospital for Sick Children-Department of Molecular Genetics-McLaughlin Centre, Botanique et Modélisation de l'Architecture des Plantes et des Végétations (UMR AMAP), Centre de Coopération Internationale en Recherche Agronomique pour le Développement (Cirad)-Institut National de la Recherche Agronomique (INRA)-Université de Montpellier (UM)-Centre National de la Recherche Scientifique (CNRS)-Institut de Recherche pour le Développement (IRD [France-Sud]), Centro de Investigación Oceanográfica en el Pacífico Sur Oriental (COPAS), Universidad de Concepción [Chile], Department of Biology, Pennsylvania State University (Penn State), Penn State System-Penn State System, Department of Biological Science [Tallahassee], Florida State University [Tallahassee] (FSU), Department of Forest Resources, University of Minnesota [Twin Cities], University of Minnesota System-University of Minnesota System, WSL Institute for Snow and Avalanche Research SLF, Communication Systems Group [Zurich], Eidgenössische Technische Hochschule - Swiss Federal Institute of Technology in Zürich [Zürich] (ETH Zürich), Academia Sinica, Facultad Ciencias del Mar, universidad catolica del Norte, Marine Biology Section, Ghent University [Belgium] (UGENT), Department of Avian Ecology, Wrocław University, Plymouth Marine Laboratory (PML), Plymouth Marine Laboratory, Institute for Marine and Antarctic Studies [Horbat] (IMAS), University of Tasmania (UTAS), European Project: 610028,EC:FP7:ERC,ERC-2013-SyG,IMBALANCE-P(2014), Dornelas, Maria, University of St Andrews. School of Biology, University of St Andrews. Fish Behaviour and Biodiversity Research Group, University of St Andrews. Marine Alliance for Science & Technology Scotland, University of St Andrews. Scottish Oceans Institute, University of St Andrews. Institute of Behavioural and Neural Sciences, University of St Andrews. St Andrews Sustainability Institute, University of St Andrews. Centre for Research into Ecological & Environmental Modelling, University of St Andrews. Sediment Ecology Research Group, University of St Andrews. Centre for Higher Education Research, Ministère de l'Europe et des Affaires étrangères (MEAE)-Centre National de la Recherche Scientifique (CNRS), Universitat Autònoma de Barcelona (UAB), Universidade de São Paulo = University of São Paulo (USP), Tel Aviv University (TAU), University of California [Santa Cruz] (UC Santa Cruz), University of California (UC)-University of California (UC), University of Copenhagen = Københavns Universitet (UCPH)-University of Copenhagen = Københavns Universitet (UCPH), Flødevigen Research Station (IMR), Institute of Marine Research [Bergen] (IMR), University of Bergen (UiB)-University of Bergen (UiB), Université de Toulouse (UT)-Université de Toulouse (UT)-Centre National de la Recherche Scientifique (CNRS), Université du Québec à Montréal = University of Québec in Montréal (UQAM), The Hospital for sick children [Toronto] (SickKids)-University of Toronto-Department of Molecular Genetics-McLaughlin Centre, Universidad de Concepción - University of Concepcion [Chile], University of Minnesota [Twin Cities] (UMN), Eidgenössische Technische Hochschule - Swiss Federal Institute of Technology [Zürich] (ETH Zürich), Universiteit Gent = Ghent University (UGENT), University of Wrocław [Poland] (UWr), Institute for Marine and Antarctic Studies [Hobart] (IMAS), University of Tasmania [Hobart, Australia] (UTAS), Centre National de la Recherche Scientifique (CNRS)-Institut de Recherche pour le Développement (IRD)-Université Toulouse III - Paul Sabatier (UT3), Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées, University of Toronto-The Hospital for sick children [Toronto] (SickKids)-Department of Molecular Genetics-McLaughlin Centre, Centre National de la Recherche Scientifique (CNRS)-Université de Montpellier (UM)-Institut National de la Recherche Agronomique (INRA)-Centre de Coopération Internationale en Recherche Agronomique pour le Développement (Cirad)-Institut de Recherche pour le Développement (IRD [France-Sud]), Universiteit Gent = Ghent University [Belgium] (UGENT), Dornelas M., Antao L.H., Moyes F., Bates A.E., Magurran A.E., Adam D., Akhmetzhanova A.A., Appeltans W., Arcos J.M., Arnold H., Ayyappan N., Badihi G., Baird A.H., Barbosa M., Barreto T.E., Bassler C., Bellgrove A., Belmaker J., Benedetti-Cecchi L., Bett B.J., Bjorkman A.D., Blazewicz M., Blowes S.A., Bloch C.P., Bonebrake T.C., Boyd S., Bradford M., Brooks A.J., Brown J.H., Bruelheide H., Budy P., Carvalho F., Castaneda-Moya E., Chen C.A., Chamblee J.F., Chase T.J., Siegwart Collier L., Collinge S.K., Condit R., Cooper E.J., Cornelissen J.H.C., Cotano U., Kyle Crow S., Damasceno G., Davies C.H., Davis R.A., Day F.P., Degraer S., Doherty T.S., Dunn T.E., Durigan G., Duffy J.E., Edelist D., Edgar G.J., Elahi R., Elmendorf S.C., Enemar A., Ernest S.K.M., Escribano R., Estiarte M., Evans B.S., Fan T.-Y., Turini Farah F., Loureiro Fernandes L., Farneda F.Z., Fidelis A., Fitt R., Fosaa A.M., Daher Correa Franco G.A., Frank G.E., Fraser W.R., Garcia H., Cazzolla Gatti R., Givan O., Gorgone-Barbosa E., Gould W.A., Gries C., Grossman G.D., Gutierrez J.R., Hale S., Harmon M.E., Harte J., Haskins G., Henshaw D.L., Hermanutz L., Hidalgo P., Higuchi P., Hoey A., Van Hoey G., Hofgaard A., Holeck K., Hollister R.D., Holmes R., Hoogenboom M., Hsieh C.-H., Hubbell S.P., Huettmann F., Huffard C.L., Hurlbert A.H., Macedo Ivanauskas N., Janik D., Jandt U., Jazdzewska A., Johannessen T., Johnstone J., Jones J., Jones F.A.M., Kang J., Kartawijaya T., Keeley E.C., Kelt D.A., Kinnear R., Klanderud K., Knutsen H., Koenig C.C., Kortz A.R., Kral K., Kuhnz L.A., Kuo C.-Y., Kushner D.J., Laguionie-Marchais C., Lancaster L.T., Min Lee C., Lefcheck J.S., Levesque E., Lightfoot D., Lloret F., Lloyd J.D., Lopez-Baucells A., Louzao M., Madin J.S., Magnusson B., Malamud S., Matthews I., McFarland K.P., McGill B., McKnight D., McLarney W.O., Meador J., Meserve P.L., Metcalfe D.J., Meyer C.F.J., Michelsen A., Milchakova N., Moens T., Moland E., Moore J., Mathias Moreira C., Muller J., Murphy G., Myers-Smith I.H., Myster R.W., Naumov A., Neat F., Nelson J.A., Paul Nelson M., Newton S.F., Norden N., Oliver J.C., Olsen E.M., Onipchenko V.G., Pabis K., Pabst R.J., Paquette A., Pardede S., Paterson D.M., Pelissier R., Penuelas J., Perez-Matus A., Pizarro O., Pomati F., Post E., Prins H.H.T., Priscu J.C., Provoost P., Prudic K.L., Pulliainen E., Ramesh B.R., Mendivil Ramos O., Rassweiler A., Rebelo J.E., Reed D.C., Reich P.B., Remillard S.M., Richardson A.J., Richardson J.P., van Rijn I., Rocha R., Rivera-Monroy V.H., Rixen C., Robinson K.P., Ribeiro Rodrigues R., de Cerqueira Rossa-Feres D., Rudstam L., Ruhl H., Ruz C.S., Sampaio E.M., Rybicki N., Rypel A., Sal S., Salgado B., Santos F.A.M., Savassi-Coutinho A.P., Scanga S., Schmidt J., Schooley R., Setiawan F., Shao K.-T., Shaver G.R., Sherman S., Sherry T.W., Sicinski J., Sievers C., da Silva A.C., Rodrigues da Silva F., Silveira F.L., Slingsby J., Smart T., Snell S.J., Soudzilovskaia N.A., Souza G.B.G., Maluf Souza F., Castro Souza V., Stallings C.D., Stanforth R., Stanley E.H., Mauro Sterza J., Stevens M., Stuart-Smith R., Rondon Suarez Y., Supp S., Yoshio Tamashiro J., Tarigan S., Thiede G.P., Thorn S., Tolvanen A., Teresa Zugliani Toniato M., Totland O., Twilley R.R., Vaitkus G., Valdivia N., Vallejo M.I., Valone T.J., Van Colen C., Vanaverbeke J., Venturoli F., Verheye H.M., Vianna M., Vieira R.P., Vrska T., Quang Vu C., Van Vu L., Waide R.B., Waldock C., Watts D., Webb S., Wesolowski T., White E.P., Widdicombe C.E., Wilgers D., Williams R., Williams S.B., Williamson M., Willig M.R., Willis T.J., Wipf S., Woods K.D., Woehler E.J., Zawada K., Zettler M.L., The Wellcome Trust, European Research Council, and University of St Andrews. Centre for Biological Diversity

Subjects
Data Papers, 0106 biological sciences, Range (biology), QH301 Biology, temporal, NERC, Biodiversity, Matematikk og Naturvitenskap: 400::Zoologiske og botaniske fag: 480 [VDP], BIALOWIEZA NATIONAL-PARK, special, computer.software_genre, [SDV.BID.SPT]Life Sciences [q-bio]/Biodiversity/Systematics, Phylogenetics and taxonomy, 01 natural sciences, species richness, SDG 15 - Life on Land, biodiversity, Global and Planetary Change, B003-ecology, Database, Ecology, Sampling (statistics), SIMULATED HERBIVORY, supporting technologies, LAND-BRIDGE ISLANDS, [SDV.BV.BOT]Life Sciences [q-bio]/Vegetal Biology/Botanics, PE&RC, global, PRIMEVAL TEMPERATE FOREST, Geography, POPULATION TRENDS, turnover, Data Paper, SECONDARY FOREST, Evolution, ESTUARINE COASTAL LAGOON, 010603 evolutionary biology, QH301, [SDV.EE.ECO]Life Sciences [q-bio]/Ecology, environment/Ecosystems, Behavior and Systematics, Anthropocene, spatial, Ecology, Evolution, Behavior and Systematics, VDP::Mathematics and natural science: 400::Zoology and botany: 480, species richne, 14. Life underwater, SDG 14 - Life Below Water, NE/L002531/1, ZA4450, Relative species abundance, ZA4450 Databases, 010604 marine biology & hydrobiology, RCUK, Biology and Life Sciences, DAS, 15. Life on land, DECIDUOUS FOREST, Taxon, Fish, 13. Climate action, MCP, Wildlife Ecology and Conservation, LONG-TERM CHANGE, Species richness, [SDE.BE]Environmental Sciences/Biodiversity and Ecology, computer, BIRD COMMUNITY DYNAMICS, VDP::Matematikk og Naturvitenskap: 400::Zoologiske og botaniske fag: 480
Abstract

Motivation The BioTIME database contains raw data on species identities and abundances in ecological assemblages through time. These data enable users to calculate temporal trends in biodiversity within and amongst assemblages using a broad range of metrics. BioTIME is being developed as a community-led open-source database of biodiversity time series. Our goal is to accelerate and facilitate quantitative analysis of temporal patterns of biodiversity in the Anthropocene. Main types of variables included The database contains 8,777,413 species abundance records, from assemblages consistently sampled for a minimum of 2 years, which need not necessarily be consecutive. In addition, the database contains metadata relating to sampling methodology and contextual information about each record. Spatial location and grain BioTIME is a global database of 547,161 unique sampling locations spanning the marine, freshwater and terrestrial realms. Grain size varies across datasets from 0.0000000158 km2 (158 cm2) to 100 km2 (1,000,000,000,000 cm2). Time period and grain BioTIME records span from 1874 to 2016. The minimal temporal grain across all datasets in BioTIME is a year. Major taxa and level of measurement BioTIME includes data from 44,440 species across the plant and animal kingdoms, ranging from plants, plankton and terrestrial invertebrates to small and large vertebrates. Software format .csv and .SQL., Global Ecology and Biogeography, 27 (7), ISSN:1466-822X, ISSN:1466-8238

Published
2018

7. Ghost Loci Imply Hox and ParaHox Existence in the Last Common Ancestor of Animals

Author

Daniel Barker, David E. K. Ferrier, and Olivia Mendivil Ramos

Subjects
Most recent common ancestor, animal structures, ParaHox, Locus (genetics), Biology, Synteny, Genome, General Biochemistry, Genetics and Molecular Biology, Homology (biology), Evolution, Molecular, Animals, Humans, Placozoa, Hox gene, Phylogeny, Genetics, Agricultural and Biological Sciences(all), Biochemistry, Genetics and Molecular Biology(all), Genes, Homeobox, Gene Expression Regulation, Developmental, Porifera, Sea Anemones, embryonic structures, Homeobox, General Agricultural and Biological Sciences, Monte Carlo Method
Abstract

Summary Hox genes are renowned for patterning animal development, with widespread roles in developmental gene regulation. Despite this importance, their evolutionary origin remains obscure, due to absence of Hox genes (and their evolutionary sisters, the ParaHox genes) from basal lineages and because the phylogenies of these genes are poorly resolved [1–7]. This has led to debate about whether Hox and ParaHox genes originated coincidently with the origin of animals or instead evolved after the divergence of the earliest animal lineages [7, 8]. Here we use genomic synteny and Monte Carlo-based simulations to resolve Hox/ParaHox origins, our approach being independent of poorly resolved homeodomain phylogenies and better able to accommodate gene loss. We show Trox-2 of placozoans occupies a ParaHox locus. In addition, a separate locus sharing synteny and hence homology with human Hox loci exists in the placozoan genome, but without a Hox-like gene in it. We call this second locus a "ghost" Hox locus, because it is homologous to the human Hox loci, but does not itself contain a Hox gene. Extending our approach to sponges, we discover distinct ghost Hox and ParaHox loci. Thus, distinct Hox and ParaHox loci were present in the last common ancestor of all living animal lineages.

Published
2012

8. Mechanisms of Gene Duplication and Translocation and Progress towards Understanding Their Relative Contributions to Animal Genome Evolution

Author

David E. K. Ferrier and Olivia Mendivil Ramos

Subjects
Whole genome sequencing, Evolutionary biology, Gene duplication, Animal genome, Review Article, Genetic Change, Biology, Bioinformatics, Gene, Genome
Abstract

Duplication of genetic material is clearly a major route to genetic change, with consequences for both evolution and disease. A variety of forms and mechanisms of duplication are recognised, operating across the scales of a few base pairs upto entire genomes. With the ever-increasing amounts of gene and genome sequence data that are becoming available, our understanding of the extent of duplication is greatly improving, both in terms of the scales of duplication events as well as their rates of occurrence. An accurate understanding of these processes is vital if we are to properly understand important events in evolution as well as mechanisms operating at the level of genome organisation. Here we will focus on duplication in animal genomes and how the duplicated sequences are distributed, with the aim of maintaining a focus on principles of evolution and organisation that are most directly applicable to the shaping of our own genome.

Published
2012

9. Genome and transcriptome of the regeneration-competent flatworm, Macrostomum lignano

Author

Peter Ladurner, M. Joaquina Delás, Kaja A. Wasik, Xin Zhou, Dita B. Vizoso, Ilaria Falciatori, W. Richard McCombie, James Gurtowski, Giorgia Battistoni, Lukas Schärer, Michael C. Schatz, Gregory J. Hannon, Andrew D. Smith, Osama El Demerdash, Olivia Mendivil Ramos, Hannon, Gregory [0000-0003-4021-3898], and Apollo - University of Cambridge Repository

Subjects
Population, Molecular Sequence Data, Helminth genetics, Computational biology, Genome, Transcriptome, Sequence Homology, Nucleic Acid, Animals, Cluster Analysis, education, Gene, genome, Genes, Helminth, Phylogeny, Genetics, Macrostomum lignano, neoblast, education.field_of_study, Genome, Helminth, Multidisciplinary, Macrostomum, biology, Base Sequence, Gene Expression Profiling, Stem Cells, Helminth Proteins, Biological Sciences, biology.organism_classification, Gene Ontology, Platyhelminths, regeneration, Reference genome, flatworm
Abstract

The free-living flatworm, Macrostomum lignano has an impressive regenerative capacity. Following injury, it can regenerate almost an entirely new organism because of the presence of an abundant somatic stem cell population, the neoblasts. This set of unique properties makes many flatworms attractive organisms for studying the evolution of pathways involved in tissue self-renewal, cell-fate specification, and regeneration. The use of these organisms as models, however, is hampered by the lack of a well-assembled and annotated genome sequences, fundamental to modern genetic and molecular studies. Here we report the genomic sequence of M. lignano and an accompanying characterization of its transcriptome. The genome structure of M. lignano is remarkably complex, with ∼75% of its sequence being comprised of simple repeats and transposon sequences. This has made high-quality assembly from Illumina reads alone impossible (N50 = 222 bp). We therefore generated 130× coverage by long sequencing reads from the Pacific Biosciences platform to create a substantially improved assembly with an N50 of 64 Kbp. We complemented the reference genome with an assembled and annotated transcriptome, and used both of these datasets in combination to probe gene-expression patterns during regeneration, examining pathways important to stem cell function.

Published
2015

10. Calcisponges have a ParaHox gene and dynamic expression of dispersed NK homeobox genes

Author

Sofia A. V. Fortunato, Maja Adamska, Jing Liu, Olivia Mendivil Ramos, Marcin Adamski, Sven Leininger, David E. K. Ferrier, University of St Andrews. School of Biology, University of St Andrews. Marine Alliance for Science & Technology Scotland, and University of St Andrews. Scottish Oceans Institute

Subjects
Genetics, Homeodomain Proteins, animal structures, Multidisciplinary, biology, QH301 Biology, Genes, Homeobox, ParaHox, Sycon, Sycon ciliatum, Antennapedia, biology.organism_classification, Genome, Amphimedon queenslandica, Synteny, Porifera, QH301, Gene Expression Regulation, Homeobox, Animals, BDC, Hox gene, R2C, Phylogeny, Body Patterning
Abstract

This study was funded by the Sars Centre core budget to M. Adamska. Sequencing was performed at the Norwegian High Throughput Sequencing Centre funded by the Norwegian Research Council. O.M.R. and D.E.K.F. acknowledge support from the BBSRC and the School of Biology, University of St Andrews. Sponges are simple animals with few cell types, but their genomes paradoxically contain a wide variety of developmental transcription factors1,2,3,4, including homeobox genes belonging to the Antennapedia (ANTP) class5,6, which in bilaterians encompass Hox, ParaHox and NK genes. In the genome of the demosponge Amphimedon queenslandica, no Hox or ParaHox genes are present, but NK genes are linked in a tight cluster similar to the NK clusters of bilaterians5. It has been proposed that Hox and ParaHox genes originated from NK cluster genes after divergence of sponges from the lineage leading to cnidarians and bilaterians5,7. On the other hand, synteny analysis lends support to the notion that the absence of Hox and ParaHox genes in Amphimedon is a result of secondary loss (the ghost locus hypothesis)8. Here we analysed complete suites of ANTP-class homeoboxes in two calcareous sponges, Sycon ciliatum and Leucosolenia complicata. Our phylogenetic analyses demonstrate that these calcisponges possess orthologues of bilaterian NK genes (Hex, Hmx and Msx), a varying number of additional NK genes and one ParaHox gene, Cdx. Despite the generation of scaffolds spanning multiple genes, we find no evidence of clustering of Sycon NK genes. All Sycon ANTP-class genes are developmentally expressed, with patterns suggesting their involvement in cell type specification in embryos and adults, metamorphosis and body plan patterning. These results demonstrate that ParaHox genes predate the origin of sponges, thus confirming the ghost locus hypothesis8, and highlight the need to analyse the genomes of multiple sponge lineages to obtain a complete picture of the ancestral composition of the first animal genome. Postprint

Published
2014

11. The First Myriapod Genome Sequence Reveals Conservative Arthropod Gene Content and Genome Organisation in the Centipede Strigamia maritima

Author

Shobha Patil, Tobias Neumann, Julio Rozas, William J. Gillis, Nicholas H. Putman, Elizabeth A. Goodwin-Horn, Jerome H.L. Hui, Andrew M. Schurko, Jiaxin Qu, François Lapraz, Peshtewani K. Aqrawi, DeNard Simmons, Michael Holder, Maria Ninova, Sam Griffiths-Jones, Dieter Ebert, Huaiyang Jiang, Jack E. Green, Shalini N. Jhangiani, Sai Gubbala, Zivkos Apostolou, Luke Hayden, Wallace Arthur, Liezl Francisco, Kim C. Worley, Marcus Coyle, Claudio R. Alonso, Peter D. Evans, Viktoriya Korchina, Montserrat Torres-Oliva, Ling-Ling Pu, Sophie Helbing, Eckart Stolle, Judith H. Willis, Christopher Pham, Pedro Patraquim, Nehad Saada, Yuanqing Wu, Christie Kovar, David E. K. Ferrier, Nathan J. Kenny, Dinh Ngoc Ngo, James M Williams, Cornelius Eibner, Kenneth W. Siggens, Tittu Mathew, Ariel D. Chipman, Robert Mata, Vera S. Hunnekuhl, Cornelis J. P. Grimmelikhuijzen, Tamsin E. M. Jones, Kristin Tessmar-Raible, Olivia Mendivil Ramos, Xiaoyan Zou, Divya Kalra, Stephen Richards, Louis Du Pasquier, Marco Mariotti, Hugh M. Robertson, Jennifer C. J. Barna, Michael Akam, Geoffrey Okwuonu, Matthew Ronshaugen, Arndt von Haeseler, Julia P. Hunn, Francisca C. Almeida, Daniela Brites, Maximilian J. Telford, Galina Erikson, William J. Palmer, Francis M. Jiggins, Kerstin P. Blankenburg, Tobias S. Kaiser, Toni Gabaldón, Helen E. Robertson, Maurijn van der Zee, Rebecca Thornton, Donna M. Muzny, Peter K. Dearden, Richard A. Gibbs, Gerard Manning, Elizabeth J. Duncan, LaRonda Jackson, Daniel S.T. Hughes, Steven E. Scherer, Reinhard Schröder, Paul Havlak, Daniel Lawson, Carlo Brena, Fiona Ongeri, Frank Hauser, Anna Stief, Mehwish Javaid, Salvador Capella-Gutierrez, Jie Lv, F. Bernhard Kraus, Irene Newsham, Roderic Guigó, Alejandro Sánchez-Gracia, Sandra L. Lee, Nadia Znassi, Yi Han, Catherine Rabouille, Adelaide C. Rhodes, Christigale Mandapat, Cassandra G. Extavour, Jiggins, Francis [0000-0001-7470-8157], Akam, Michael [0000-0003-0063-2297], Apollo - University of Cambridge Repository, Hubrecht Institute for Developmental Biology and Stem Cell Research, University of St Andrews. School of Biology, University of St Andrews. Marine Alliance for Science & Technology Scotland, and University of St Andrews. Scottish Oceans Institute

Subjects
Evolutionary Genetics, Male, 0106 biological sciences, RNA, Untranslated, Gene family evolution, Lydia Becker Institute, Animal Evolution, QH301 Biology, Biología, Receptors, Odorant, 01 natural sciences, Genome, purl.org/becyt/ford/1 [https], Genética y Herencia, Genome Sequencing, Biology (General), Selenoproteins, Genome Evolution, R2C, Phylogeny, Genetics, 0303 health sciences, Phylogenetic analysis, Sex Chromosomes, biology, Myriapoda, Circadian Rhythm Signaling Peptides and Proteins, General Neuroscience, ~DC~, Gene content, Genomics, Insects, Drosophila melanogaster, Multigene Family, QH0426, Female, BDC, General Agricultural and Biological Sciences, CIENCIAS NATURALES Y EXACTAS, Research Article, Genome evolution, Evolutionary Immunology, Arthropoda, QH301-705.5, Genome Complexity, Synteny, 010603 evolutionary biology, General Biochemistry, Genetics and Molecular Biology, Ciencias Biológicas, Evolution, Molecular, QH301, Invertebrate genomics, 03 medical and health sciences, ResearchInstitutes_Networks_Beacons/lydia_becker_institute_of_immunology_and_inflammation, Homeobox, Animals, Gene family, purl.org/becyt/ford/1.6 [https], Molecular Biology Techniques, Sequencing Techniques, Molecular Biology, Arthropods, Gene, Institut für Biochemie und Biologie, 030304 developmental biology, Comparative genomics, Evolutionary Biology, Polymorphism, Genetic, General Immunology and Microbiology, Genètica animal, Human evolutionary genetics, fungi, Biology and Life Sciences, Computational Biology, Genètica evolutiva, DNA Methylation, Comparative Genomics, biology.organism_classification, Hormones, Organismal Evolution, Genome, Mitochondrial, Arthropod, Protein Kinases, Transcription Factors
Abstract

Myriapods (e.g., centipedes and millipedes) display a simple homonomous body plan relative to other arthropods. All members of the class are terrestrial, but they attained terrestriality independently of insects. Myriapoda is the only arthropod class not represented by a sequenced genome. We present an analysis of the genome of the centipede Strigamia maritima. It retains a compact genome that has undergone less gene loss and shuffling than previously sequenced arthropods, and many orthologues of genes conserved from the bilaterian ancestor that have been lost in insects. Our analysis locates many genes in conserved macro-synteny contexts, and many small-scale examples of gene clustering. We describe several examples where S. maritima shows different solutions from insects to similar problems. The insect olfactory receptor gene family is absent from S. maritima, and olfaction in air is likely effected by expansion of other receptor gene families. For some genes S. maritima has evolved paralogues to generate coding sequence diversity, where insects use alternate splicing. This is most striking for the Dscam gene, which in Drosophila generates more than 100,000 alternate splice forms, but in S. maritima is encoded by over 100 paralogues. We see an intriguing linkage between the absence of any known photosensory proteins in a blind organism and the additional absence of canonical circadian clock genes. The phylogenetic position of myriapods allows us to identify where in arthropod phylogeny several particular molecular mechanisms and traits emerged. For example, we conclude that juvenile hormone signalling evolved with the emergence of the exoskeleton in the arthropods and that RR-1 containing cuticle proteins evolved in the lineage leading to Mandibulata. We also identify when various gene expansions and losses occurred. The genome of S. maritima offers us a unique glimpse into the ancestral arthropod genome, while also displaying many adaptations to its specific life history., Author Summary Arthropods are the most abundant animals on earth. Among them, insects clearly dominate on land, whereas crustaceans hold the title for the most diverse invertebrates in the oceans. Much is known about the biology of these groups, not least because of genomic studies of the fruit fly Drosophila, the water flea Daphnia, and other species used in research. Here we report the first genome sequence from a species belonging to a lineage that has previously received very little attention—the myriapods. Myriapods were among the first arthropods to invade the land over 400 million years ago, and survive today as the herbivorous millipedes and venomous centipedes, one of which—Strigamia maritima—we have sequenced here. We find that the genome of this centipede retains more characteristics of the presumed arthropod ancestor than other sequenced insect genomes. The genome provides access to many aspects of myriapod biology that have not been studied before, suggesting, for example, that they have diversified receptors for smell that are quite different from those used by insects. In addition, it shows specific consequences of the largely subterranean life of this particular species, which seems to have lost the genes for all known light-sensing molecules, even though it still avoids light.

Published
2014

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