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Pleiotropic and Epistatic Network-Based Discovery: Integrated Networks for Target Gene Discovery

View ORCID ProfileDeborah Weighill, Piet Jones, Manesh Shah, Priya Ranjan, Wellington Muchero, Jeremy Schmutz, Avinash Sreedasyam, David Macaya-Sanz, Robert Sykes, Nan Zhao, Madhavi Z. Martin, Stephen DiFazio, Timothy J. Tschaplinski, Gerald Tuskan, Daniel Jacobson
doi: https://doi.org/10.1101/267997
Deborah Weighill
1The Bredesen Center for Interdisciplinary Research and Graduate Education, University of Tennessee, Knoxville, Knoxville, TN, USA
2Biosciences Division, Oak Ridge National Laboratory, Oak Ridge, TN, USA
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  • ORCID record for Deborah Weighill
Piet Jones
1The Bredesen Center for Interdisciplinary Research and Graduate Education, University of Tennessee, Knoxville, Knoxville, TN, USA
2Biosciences Division, Oak Ridge National Laboratory, Oak Ridge, TN, USA
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Manesh Shah
2Biosciences Division, Oak Ridge National Laboratory, Oak Ridge, TN, USA
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Priya Ranjan
2Biosciences Division, Oak Ridge National Laboratory, Oak Ridge, TN, USA
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Wellington Muchero
2Biosciences Division, Oak Ridge National Laboratory, Oak Ridge, TN, USA
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Jeremy Schmutz
4Department of Energy Joint Genome Institute, Walnut Creek, CA, USA
5HudsonAlpha Institute for Biotechnology, Huntsville, AL, USA
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Avinash Sreedasyam
5HudsonAlpha Institute for Biotechnology, Huntsville, AL, USA
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David Macaya-Sanz
6Department of Biology, West Virginia University, Morgantown, WV, USA
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Robert Sykes
3National Renewable Energy Laboratory, Golden, CO, USA
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Nan Zhao
7The University of Tennessee Institute of Agriculture, University of Tennessee, Knoxville, Knoxville, TN, USA
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Madhavi Z. Martin
2Biosciences Division, Oak Ridge National Laboratory, Oak Ridge, TN, USA
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Stephen DiFazio
6Department of Biology, West Virginia University, Morgantown, WV, USA
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Timothy J. Tschaplinski
2Biosciences Division, Oak Ridge National Laboratory, Oak Ridge, TN, USA
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Gerald Tuskan
2Biosciences Division, Oak Ridge National Laboratory, Oak Ridge, TN, USA
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Daniel Jacobson
1The Bredesen Center for Interdisciplinary Research and Graduate Education, University of Tennessee, Knoxville, Knoxville, TN, USA
2Biosciences Division, Oak Ridge National Laboratory, Oak Ridge, TN, USA
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Abstract

Biological organisms are complex systems that are composed of functional networks of interacting molecules and macromolecules. Complex phenotypes are the result of orchestrated, hierarchical, heterogeneous collections of expressed genomic variants. However, the effects of these variants are the result of historic selective pressure and current environmental and epigenetic signals, and, as such, their co-occurrence can be seen as genome-wide correlations in a number of different manners. Biomass recalcitrance (i.e., the resistance of plants to degradation or deconstruction, which ultimately enables access to a plant’s sugars) is a complex polygenic phenotype of high importance to biofuels initiatives. This study makes use of data derived from the re-sequenced genomes from over 800 different Populus trichocarpa genotypes in combination with metabolomic and pyMBMS data across this population, as well as co-expression and co-methylation networks in order to better understand the molecular interactions involved in recalcitrance, and identify target genes involved in lignin biosynthesis/degradation. A Lines Of Evidence (LOE) scoring system is developed to integrate the information in the different layers and quantify the number of lines of evidence linking genes to lignin-related lignin-phenotypes across the network layers. The resulting Genome Wide Association Study networks, integrated with Single Nucleotide Polymorphism (SNP) correlation, co-methylation and co-expression networks through the LOE scores are proving to be a powerful approach to determine the pleiotropic and epistatic relationships underlying cellular functions and, as such, the molecular basis for complex phenotypes, such as recalcitrance.

Footnotes

  • ↵* jacobsonda{at}ornl.gov

  • This manuscript has been authored by UT-Battelle, LLC under Contract No. DE-AC05-00GR22725 with the U.S. Department of Energy. The United States Government retains and the publisher, by accepting the article for publication, acknowledges that the United States Government retains a non-exclusive, paid-up, irrevocable, worldwide license to publish or reproduce the published form of this manuscript, or allow others to do so, for United States Government purposes. The Department of Energy will provide public access to these results of federally sponsored research in accordance with the DGE Public Access Plan (http://energy.gov/downloads/doe-public-access-plan). The work conducted by the U.S. Department of Energy Joint Genome Institute is supported by the Office of Science of the U.S. Department of Energy under Contract No. DE-AC02-05CH11231.

Copyright 
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. This article is a US Government work. It is not subject to copyright under 17 USC 105 and is also made available for use under a CC0 license.
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Posted February 19, 2018.
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Pleiotropic and Epistatic Network-Based Discovery: Integrated Networks for Target Gene Discovery
Deborah Weighill, Piet Jones, Manesh Shah, Priya Ranjan, Wellington Muchero, Jeremy Schmutz, Avinash Sreedasyam, David Macaya-Sanz, Robert Sykes, Nan Zhao, Madhavi Z. Martin, Stephen DiFazio, Timothy J. Tschaplinski, Gerald Tuskan, Daniel Jacobson
bioRxiv 267997; doi: https://doi.org/10.1101/267997
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Pleiotropic and Epistatic Network-Based Discovery: Integrated Networks for Target Gene Discovery
Deborah Weighill, Piet Jones, Manesh Shah, Priya Ranjan, Wellington Muchero, Jeremy Schmutz, Avinash Sreedasyam, David Macaya-Sanz, Robert Sykes, Nan Zhao, Madhavi Z. Martin, Stephen DiFazio, Timothy J. Tschaplinski, Gerald Tuskan, Daniel Jacobson
bioRxiv 267997; doi: https://doi.org/10.1101/267997

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