A physical map for the Amborella trichopoda genome sheds light on the evolution of angiosperm genome structure
Author
Zuccolo, AndreaBowers, John
Estill, James
Xiong, Zhiyong
Luo, Meizhong
Sebastian, Aswathy
Goicoechea, Jose
Collura, Kristi
Yu, Yeisoo
Jiao, Yuannian
Duarte, Jill
Tang, Haibao
Ayyampalayam, Saravanaraj
Rounsley, Steve
Kudrna, Dave
Paterson, Andrew
Pires, J.
Chanderbali, Andre
Soltis, Douglas
Chamala, Srikar
Barbazuk, Brad
Soltis, Pamela
Albert, Victor
Ma, Hong
Mandoli, Dina
Banks, Jody
Carlson, John
Tomkins, Jeffrey
dePamphilis, Claude
Wing, Rod
Leebens-Mack, Jim
Affiliation
Arizona Genomics Institute, School of Plant Sciences and BIO5 Institute for Collaborative Research, University of Arizona, 1657 East Helen Street, Tucson, AZ 85721, USADepartment of Plant Biology, University of Georgia, 4504 Miller Plant Sciences, Athens, GA 30602, USA
Department of Biological Sciences, University of Missouri, 371B Life Sciences Center, Columbia, MO 65211, USA
College of Life Sciences and Technology, Huazhong Agricultural University, Wuhan, Hubei 430070, China
Intercollege Graduate Degree Program in Plant Biology and Institute of Molecular Evolutionary Genetics, Huck Institutes of the Life Sciences, The Pennsylvania State University, 405 Life Sciences Building, University Park, Pennsylvania 16802, USA
Department of Plant and Microbiology, College of Natural Resources, University of California, 311 Koshland Hall, Berkeley 94709, CA, USA
Plant Genome Mapping Laboratory, University of Georgia, 111 Riverbend Road, Athens, GA 30605, USA
School of Plant Sciences and BIO5, University of Arizona, 1657 East Helen Street, Tucson, AZ 85721, USA
Dow Agrosciences LLC, 9330 Zionsville Road, Indianapolis, IN 46268, USA
Department of Biology, University of Florida, 220 Bartram Hall, Gainesville, FL 32611, USA
Florida Museum of Natural History, Museum Road and Newell Drive, University of Florida, Gainesville, FL 32611, USA
Department of Biological Sciences, University at Buffalo (SUNY), 637 Hochstetter Hall, Buffalo, NY 14260, USA
State Key Laboratory of Genetic Engineering, School of Life Sciences, Institute of Plant Biology, Center for Evolutionary Biology, and Institutes of Biomedical Sciences, Fudan University, 220 Handan Road, Shanghai 200433, China
Northern Lights, 4500 NE 40th Street, Seattle WA 98105, USA
Department of Botany and Plant Pathology, Purdue University, B028 Whistler Hall, West Lafayette, IN 47906, USA
School of Forest Resources, The Pennsylvania State University, 323 Forest Resources Building, University Park, PA 16802, USA
Clemson University Genomics Institute, Clemson University, 51 Cherry St, Clemson, NC 29634, USA
Issue Date
2011
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BioMed CentralCitation
Zuccolo et al. Genome Biology 2011, 12:R48 http://genomebiology.com/2011/12/5/R48Journal
Genome BiologyRights
© 2011 Zuccolo et al.; licensee BioMed Central Ltd. This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0).Collection Information
This item is part of the UA Faculty Publications collection. For more information this item or other items in the UA Campus Repository, contact the University of Arizona Libraries at repository@u.library.arizona.edu.Abstract
BACKGROUND:Recent phylogenetic analyses have identified Amborella trichopoda, an understory tree species endemic to the forests of New Caledonia, as sister to a clade including all other known flowering plant species. The Amborella genome is a unique reference for understanding the evolution of angiosperm genomes because it can serve as an outgroup to root comparative analyses. A physical map, BAC end sequences and sample shotgun sequences provide a first view of the 870 Mbp Amborella genome.RESULTS:Analysis of Amborella BAC ends sequenced from each contig suggests that the density of long terminal repeat retrotransposons is negatively correlated with that of protein coding genes. Syntenic, presumably ancestral, gene blocks were identified in comparisons of the Amborella BAC contigs and the sequenced Arabidopsis thaliana, Populus trichocarpa, Vitis vinifera and Oryza sativa genomes. Parsimony mapping of the loss of synteny corroborates previous analyses suggesting that the rate of structural change has been more rapid on lineages leading to Arabidopsis and Oryza compared with lineages leading to Populus and Vitis. The gamma paleohexiploidy event identified in the Arabidopsis, Populus and Vitis genomes is shown to have occurred after the divergence of all other known angiosperms from the lineage leading to Amborella.CONCLUSIONS:When placed in the context of a physical map, BAC end sequences representing just 5.4% of the Amborella genome have facilitated reconstruction of gene blocks that existed in the last common ancestor of all flowering plants. The Amborella genome is an invaluable reference for inferences concerning the ancestral angiosperm and subsequent genome evolution.Version
Final published versionAdditional Links
http://genomebiology.com/2011/12/5/R48ae974a485f413a2113503eed53cd6c53
10.1186/gb-2011-12-5-r48
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Except where otherwise noted, this item's license is described as © 2011 Zuccolo et al.; licensee BioMed Central Ltd. This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0).

