Location: Plant Genetic Resources Conservation Unit
Title: Genomic mechanisms of climate adaptation in polyploid bioenergy switchgrassAuthor
LOVELL, JOHN - Genome Sequencing Center | |
MACQUEEN, ALICE - University Of Texas | |
MAMIDI, SUJAN - Genome Sequencing Center | |
BONNETTE, JASON - University Of Texas | |
JENKINS, JERRY - Genome Sequencing Center | |
NAPIER, JOSEPH - University Of Texas | |
SREEDASYAM, AVINASH - Genome Sequencing Center | |
HEALEY, ADAM - Genome Sequencing Center | |
SESSION, ADAM - Energy Joint Genome Institute | |
SHU, SHENGQUIANG - Energy Joint Genome Institute | |
BARRY, KERRIE - Energy Joint Genome Institute | |
BONOS, STACEY - Rutgers University | |
BOSTON, LORIBETH - Genome Sequencing Center | |
DAUM, CHRISTOPHER - Energy Joint Genome Institute | |
DESHPANDE, SHWETA - Energy Joint Genome Institute | |
EWING, AREN - Energy Joint Genome Institute | |
GRABOWSKI, PAUL - Genome Sequencing Center | |
HAQUE, TASLIMA - University Of Texas | |
Harrison, Melanie | |
JIANG, JIMING - Michigan State University | |
KUDRNA, DAVE - University Of Arizona | |
LIPZEN, ANNA - Energy Joint Genome Institute | |
PENDERGAST IV, THOMAS - University Of Georgia | |
PLOTT, CHRIS - Genome Sequencing Center | |
QI, PENG - University Of Georgia | |
SASKI, CHRISTOPHER - Clemson University | |
SHAKIROV, EUGENE - University Of Texas | |
SIMS, DAVID - Genome Sequencing Center | |
SHARMA, MANOJ - Jawaharlal Nehru University | |
SHARMA, RITA - Jawaharlal Nehru University | |
STEWART, ADA - Genome Sequencing Center | |
SINGAN, VASANTH - Energy Joint Genome Institute | |
TANG, YUHONG - Noble Research Institute | |
THIBIVILLIER, SANDRA - Non ARS Employee | |
WEBBER, JENELL - Genome Sequencing Center | |
WENG, XIAOYU - University Of Texas | |
WILLIAMS, MELISSA - Genome Sequencing Center | |
WU, ALBERT - Energy Joint Genome Institute | |
YOSHINAGA, YUKO - Energy Joint Genome Institute | |
ZANE, MATTHEW - Energy Joint Genome Institute | |
ZHANG, LI - Genome Sequencing Center | |
ZHANG, JIYI - University Of Georgia | |
BEHRMAN, KATHERINE - University Of Texas At Austin | |
BOE, ARVID - South Dakota State University | |
Fay, Philip | |
FRITSCHI, FELIX - University Of Missouri | |
JASTRO, JULIE - Argonne National Laboratory | |
LLOYD-REILLEY, JOHN - US Department Of Agriculture (USDA) | |
MARTINEZ-REYNA, JUAN MANUEL - Argonne National Laboratory | |
MATAMALA, ROSER - Argonne National Laboratory | |
Mitchell, Robert - Rob | |
ROUQUETTE JR., FRANCIS - Texas A&M Agrilife | |
RONALD, PAM - University Of California, Davis | |
SAHA, MALAY - Noble Research Institute | |
Tobias, Christian | |
UDVARDI, MICHAEL - Noble Research Institute | |
WING, ROD - University Of Arizona | |
WU, YANQI - Oklahoma State University | |
BARTLEY, LAURA - University Of Oklahoma | |
Casler, Michael | |
DEVOS, KATRIEN - University Of Georgia | |
LOWRY, DAVID - Michigan State University | |
ROKHSAR, DAN - Energy Joint Genome Institute | |
GRIMWOOD, JANE - Genome Sequencing Center | |
JUENGER, THOMAS - University Of Texas | |
SCHMUTZ, JEREMY - Genome Sequencing Center |
Submitted to: Nature Genetics
Publication Type: Peer Reviewed Journal Publication Acceptance Date: 12/16/2020 Publication Date: 1/27/2021 Citation: Lovell, J.T., MacQueen, A.H., Mamidi, S., Bonnette, J., Jenkins, J., Napier, J.D., Sreedasyam, A., Healey, A., Session, A., Shu, S., Barry, K., Bonos, S., Boston, L., Daum, C., Deshpande, S., Ewing, A., Grabowski, P., Haque, T., Harrison, M.L., Jiang, J., Kudrna, D., Lipzen, A., Pendergast IV, T.H., Plott, C., Qi, P., Saski, C.A., Shakirov, E., Sims, D., Sharma, M., Sharma, R., Stewart, A., Singan, V., Tang, Y., Thibivillier, S., Webber, J., Weng, X., Williams, M., Wu, A., Yoshinaga, Y., Zane, M., Zhang, L., Zhang, J., Behrman, K.D., Boe, A.R., Fay, P.A., Fritschi, F.B., Jastro, J.D., Lloyd-Reilley, J., Martinez-Reyna, J., Matamala, R., Mitchell, R., Rouquette Jr., F.M., Ronald, P., Saha, M., Tobias, C.M., Udvardi, M., Wing, R., Wu, Y., Bartley, L.E., Casler, M.D., Devos, K.M., Lowry, D.B., Rokhsar, D., Grimwood, J., Juenger, T.E., Schmutz, J. 2021. Genomic mechanisms of climate adaptation in polyploid bioenergy switchgrass. Nature Genetics. 590:438-444. https://doi.org/10.1038/s41586-020-03127-1. DOI: https://doi.org/10.1038/s41586-020-03127-1 Interpretive Summary: Switchgrass is a perennial grass undergoing development as a candidate for biomass production in support of an emerging bioenergy and bioproducts industry. The genetics of switchgrass are complex, so knowledge of the organization of its genome and its evolutionary history are critical to support development of new adapted varieties to optimize biomass production across the broad geographic range of switchgrass. This paper reports a team effort to develop a comprehensive DNA sequence of the entire switchgrass genome, combined with a comprehensive analysis of its evolutionary history. This analysis revealed three distinct switchgrass populations: Gulf Coast, Atlantic, and Midwest. These populations form distinct gene pools that form a basis for breeding and selection to develop varieties suitable for use in diverse agricultural systems and environments. These results represent a huge step forward in understanding the genetic structure of this candidate bioenergy crop and the evolution of one of the most widespread and abundant native perennial grasses in North America. More broadly, the complete switchgrass genome will open new avenues through which native grasses can benefit agriculture and conservation. Technical Abstract: Long term climate change and periodic environmental extremes threaten food and fuel security and global crop productivity in general. While molecular and adaptive breeding strategies can buffer the effects of climatic stress and improve crop resilience, these approaches require sufficient knowledge of the genes that underlie productivity and adaptation — knowledge that until now has been limited to the minority of plants with small, inbred or diploid genomes. Here, we present the complete genome assembly and annotation for the biofuel crop switchgrass, the first for an outbred polyploid plant. We leverage these genome resources and phenotypes from ten common gardens to build a database of climate-yield-gene associations and to dissect the impact of outcrossing and polyploidy on switchgrass adaptive evolution. Outcrossing has accelerated adaptation to and postglacial colonization of northern climates through introgression of alleles from a pre-adapted northern gene pool, while polyploidy has facilitated adaptation through fractionation of gene function and the surprising discovery of highly elevated heritable genetic diversity on the non-dominant subgenome. This interplay between molecular evolution, polyploidy, outcrossing and local adaptation would have been obscured without a complete genome sequence and annotation. Combined, the genome resources and gene-trait associations developed here provide breeders with necessary tools to expand the per-hectare yield and climate envelope of economically sustainable biofuel production. |