Genome of the Asian longhorned beetle (Anoplophora glabripennis), a globally significant invasive species, reveals key functional and evolutionary innovations at the beetle–plant interface
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McKenna, Duane D.Scully, Erin D.
Pauchet, Yannick
Hoover, Kelli
Kirsch, Roy
Geib, Scott M.
Mitchell, Robert F.
Waterhouse, Robert M.
Ahn, Seung-Joon
Arsala, Deanna
Benoit, Joshua B.
Blackmon, Heath
Bledsoe, Tiffany
Bowsher, Julia H.
Busch, André
Calla, Bernarda
Chao, Hsu
Childers, Anna K.
Childers, Christopher
Clarke, Dave J.
Cohen, Lorna
Demuth, Jeffery P.
Dinh, Huyen
Doddapaneni, HarshaVardhan
Dolan, Amanda
Duan, Jian J.
Dugan, Shannon
Friedrich, Markus
Glastad, Karl M.
Goodisman, Michael A. D.
Haddad, Stephanie
Han, Yi
Hughes, Daniel S. T.
Ioannidis, Panagiotis
Johnston, J. Spencer
Jones, Jeffery W.
Kuhn, Leslie A.
Lance, David R.
Lee, Chien-Yueh
Lee, Sandra L.
Lin, Han
Lynch, Jeremy A.
Moczek, Armin P.
Murali, Shwetha C.
Muzny, Donna M.
Nelson, David R.
Palli, Subba R.
Panfilio, Kristen A.
Pers, Dan
Poelchau, Monica F.
Quan, Honghu
Qu, Jiaxin
Ray, Ann M.
Rinehart, Joseph P.
Robertson, Hugh M.
Roehrdanz, Richard
Rosendale, Andrew J.
Shin, Seunggwan
Silva, Christian
Torson, Alex S.
Jentzsch, Iris M. Vargas
Werren, John H.
Worley, Kim C.
Yocum, George
Zdobnov, Evgeny M.
Gibbs, Richard A.
Richards, Stephen
Affiliation
Univ Arizona, Ctr Insect SciUniv Arizona, Dept Neurosci
Issue Date
2016-11-11Keywords
ChemoperceptionDetoxification
Glycoside hydrolase
Horizontal gene transfer
Phytophagy
Xylophagy
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BIOMED CENTRAL LTDCitation
Genome of the Asian longhorned beetle (Anoplophora glabripennis), a globally significant invasive species, reveals key functional and evolutionary innovations at the beetle–plant interface 2016, 17 (1) Genome BiologyJournal
Genome BiologyRights
© The Author(s). 2016 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0.Collection Information
This item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.Abstract
Background: Relatively little is known about the genomic basis and evolution of wood- feeding in beetles. We undertook genome sequencing and annotation, gene expression assays, studies of plant cell wall degrading enzymes, and other functional and comparative studies of the Asian longhorned beetle, Anoplophora glabripennis, a globally significant invasive species capable of inflicting severe feeding damage on many important tree species. Complementary studies of genes encoding enzymes involved in digestion of woody plant tissues or detoxification of plant allelochemicals were undertaken with the genomes of 14 additional insects, including the newly sequenced emerald ash borer and bull-headed dung beetle. Results: The Asian longhorned beetle genome encodes a uniquely diverse arsenal of enzymes that can degrade the main polysaccharide networks in plant cell walls, detoxify plant allelochemicals, and otherwise facilitate feeding on woody plants. It has the metabolic plasticity needed to feed on diverse plant species, contributing to its highly invasive nature. Large expansions of chemosensory genes involved in the reception of pheromones and plant kairomones are consistent with the complexity of chemical cues it uses to find host plants and mates. Conclusions: Amplification and functional divergence of genes associated with specialized feeding on plants, including genes originally obtained via horizontal gene transfer from fungi and bacteria, contributed to the addition, expansion, and enhancement of the metabolic repertoire of the Asian longhorned beetle, certain other phytophagous beetles, and to a lesser degree, other phytophagous insects. Our results thus begin to establish a genomic basis for the evolutionary success of beetles on plants.Note
Open access journalISSN
1474-760XVersion
Final published versionSponsors
NHGRI [U54 HG003273]; University of Memphis FedEx Institute; US NSF [DEB1355169]; USDA-APHIS cooperative agreement [15-8130-0547-CA]; USDA NIFA [2015-67013-23287]; NSF [IOS1120209, IOS1256689, DEB1257053]; University of Cincinnati Faculty Development Research grant; Marie Curie International Outgoing Fellowship [PIOF-GA-2011-303312]; Swiss NSF awards [31003A-125350, 31003A-143936]; Max-Planck-Gesellschaft; German Research Foundation (DFG) [PA 2044/1-1, SFB 680]; NIH postdoctoral training grant [5 K12 GM000708-15]ae974a485f413a2113503eed53cd6c53
10.1186/s13059-016-1088-8
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Except where otherwise noted, this item's license is described as © The Author(s). 2016 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0.

