JMJessica E. Mattick

Jessica E. Mattick

*This is an algorithmically generated author record based on publicly available information.

Current Organizations / Institutes

The organizations/institutes from the scholar's latest article


Jessica E. Mattick has a total of 41 co-authors. Here are the top co-authors by number of shared publications:

  • Adam Barling

    Department of Crop Sciences, University of Illinois, 1102S Goodwin Ave, Urbana, IL, 61801, USA

    1 shared publication
  • Adam M. Session

    Department of Molecular and Cell Biology, University of California, Berkeley, CA, 94720, USA

    1 shared publication
  • Adebosola Oladeinde

    Department of Crop Sciences, University of Illinois, 1102S Goodwin Ave, Urbana, IL, 61801, USA

    1 shared publication
  • Bimal Kumar Ghimire

    Department of Applied Bioscience, Konkuk University, Seoul, 05029, Republic of Korea

    1 shared publication
  • Brandon T. James

    DOE Center for Advanced Bioenergy and Bioproducts Innovation, University of Illinois Urbana-Champaign

    1 shared publication
  • Chang Yeon Yu

    Department of Applied Plant Sciences, Kangwon National University, Chuncheon, Gangwon, 200-701, Republic of Korea

    1 shared publication

Latest Publications

  • Open Access

    Genome biology of the paleotetraploid perennial biomass crop Miscanthus

    by Therese Mitros, Adam M. Session, Brandon T. James, Guohong Albert Wu, Mohammad B. Belaffif, Lindsay V. Clark, Shengqiang Shu, Hongxu Dong, Adam Barling, Jessica R. Holmes, et al.

    Miscanthus is a perennial wild grass that is of global importance for paper production, roofing, horticultural plantings, and an emerging highly productive temperate biomass crop. We report a chromosome-scale assembly of the paleotetraploid M. sinensis genome, providing a resource for Miscanthus that links its chromosomes to the related diploid Sorghum and complex polyploid sugarcanes. The asymmetric distribution of transposons across the two homoeologous subgenomes proves Miscanthus paleo-allotetraploidy and identifies several balanced reciprocal homoeologous exchanges. Analysis of M. sinensis and M. sacchariflorus populations demonstrates extensive interspecific admixture and hybridization, and documents the origin of the highly productive triploid bioenergy crop M. × giganteus. Transcriptional profiling of leaves, stem, and rhizomes over growing seasons provides insight into rhizome development and nutrient recycling, processes critical for sustainable biomass accumulation in a perennial temperate grass. The Miscanthus genome expands the power of comparative genomics to understand traits of importance to Andropogoneae grasses.