Location: Bee Research Laboratory
Title: Why sequence all eukaryotes?Author
BLAXTER, MARK - Wellcome Trust Sanger Institute | |
ARCHIBALD, JOHN - Dalhousie University | |
Childers, Anna | |
CODDINGTON, JONATHAN - Smithsonian Institute | |
CRANDALL, KEITH - George Washington University Medical Center | |
DIPALMA, FEDERICA - University Of East Anglia | |
DURBIN, RICHARD - Wellcome Trust Sanger Institute | |
EDWARDS, SCOTT - Harvard University | |
GRAVES, JENNIFER - University Of Canberra | |
Hackett, Kevin | |
HALL, NEIL - Earlham Institute | |
JARVIS, ERICH - Rockefeller University | |
JOHNSON, REBECCA - Smithsonian Institute | |
KARLSSON, ELINOR - Broad Institute Of Mit/harvard | |
KRESS, JOHN - Smithsonian Institute | |
KURAKU, SHIGEHIRO - Riken Institute | |
LAWNICZAK, MARA - Wellcome Trust Sanger Institute | |
LINDBLAD-TOH, KERSTIN - Broad Institute Of Mit/harvard | |
LOPEZ, JOSE - Nova Southeastern University | |
MORAN, NANCY - University Of Texas At Austin | |
ROBINSON, GENE - University Of Illinois | |
RYDER, OLIVER - University Of California, San Diego | |
SHAPIRO, BETH - University Of California Santa Cruz | |
SOLTIS, PAMELA - University Of Florida | |
WARNOW, TANDY - University Of Illinois | |
ZHANG, GUOJIE - University Of Copenhagen | |
LEWIN, HARRIS - University Of California, Davis |
Submitted to: Proceedings of the National Academy of Sciences (PNAS)
Publication Type: Other Publication Acceptance Date: 11/1/2021 Publication Date: 1/18/2022 Citation: Blaxter, M.L., Archibald, J.M., Childers, A.K., Coddington, J.A., Crandall, K.A., Dipalma, F., Durbin, R., Edwards, S.V., Graves, J.A., Hackett, K.J., Hall, N., Jarvis, E.D., Johnson, R.N., Karlsson, E.K., Kress, J.W., Kuraku, S., Lawniczak, M.K., Lindblad-Toh, K., Lopez, J., Moran, N.A., Robinson, G.E., Ryder, O.A., Shapiro, B., Soltis, P.S., Warnow, T., Zhang, G., Lewin, H.A. 2022. Why sequence all eukaryotes?. Proceedings of the National Academy of Sciences(PNAS). 119:(4) e2115636118. https://doi.org/10.1073/pnas.2115636118. DOI: https://doi.org/10.1073/pnas.2115636118 Interpretive Summary: Life on Earth has evolved from initial simplicity to the astounding complexity we experience today. Bacteria and archaea have largely excelled in metabolic diversification, but eukaryotes additionally display abundant morphological innovation. How have these innovations come about and what constraints are there on the origins of novelty and the continuing maintenance of biodiversity on Earth? The history of life and the code for the working parts of cells and systems are written in the genome. The Earth BioGenome Project has proposed that the genomes of all extant, named eukaryotes—about 2 million species—should be sequenced to high quality to produce a digital library of life on Earth, beginning with strategic phylogenetic, ecological, and high-impact priorities. Here we discuss why we should sequence all eukaryotic species, not just a representative few scattered across the many branches of the tree of life. We suggest that many questions of evolutionary and ecological significance will only be addressable when whole-genome data representing divergences at all of the branchings in the tree of life or all species in natural ecosystems are available. We envisage that a genomic tree of life will foster understanding of the ongoing processes of speciation, adaptation, and organismal dependencies within entire ecosystems. These explorations will resolve long-standing problems in phylogenetics, evolution, ecology, conservation, agriculture, bioindustry, and medicine. Technical Abstract: Life on Earth has evolved from initial simplicity to the astounding complexity we experience today. Bacteria and archaea have largely excelled in metabolic diversification, but eukaryotes additionally display abundant morphological innovation. How have these innovations come about and what constraints are there on the origins of novelty and the continuing maintenance of biodiversity on Earth? The history of life and the code for the working parts of cells and systems are written in the genome. The Earth BioGenome Project has proposed that the genomes of all extant, named eukaryotes—about 2 million species—should be sequenced to high quality to produce a digital library of life on Earth, beginning with strategic phylogenetic, ecological, and high-impact priorities. Here we discuss why we should sequence all eukaryotic species, not just a representative few scattered across the many branches of the tree of life. We suggest that many questions of evolutionary and ecological significance will only be addressable when whole-genome data representing divergences at all of the branchings in the tree of life or all species in natural ecosystems are available. We envisage that a genomic tree of life will foster understanding of the ongoing processes of speciation, adaptation, and organismal dependencies within entire ecosystems. These explorations will resolve long-standing problems in phylogenetics, evolution, ecology, conservation, agriculture, bioindustry, and medicine. |