Skip to main content
ARS Home » Plains Area » El Reno, Oklahoma » Grazinglands Research Laboratory » Forage and Livestock Production Research » Research » Publications at this Location » Publication #335622

Research Project: Integrated Forage Systems for Food and Energy Production in the Southern Great Plains

Location: Forage and Livestock Production Research

Title: Utilization of flow cytometry to identify chimeral sectors in leaf tissue of Lolium multiflorum x L. arundinaceum hybrids

Author
item Kindiger, Bryan

Submitted to: Plant and Animal Genome Conference Proceedings
Publication Type: Abstract Only
Publication Acceptance Date: 11/15/2016
Publication Date: 1/13/2017
Citation: Kindiger, B.K. 2017. Utilization of flow cytometry to identify chimeral sectors in leaf tissue of Lolium multiflorum x L. arundinaceum hybrids [abstract]. Plant and Animal Genome Conference, January 14-18, 2017, San Diego, California. Pg. 16. Available: http://www.intlpag.org/2017/images/pdf/PAGXXV-abstracts-posters.pdf.

Interpretive Summary: Abstract only.

Technical Abstract: We have identified a method whereby Lolium multiflorum (Lm) or L. arundinaceum (Fa) genomes are preferentially eliminated through a mitotic loss behavior in interspecific Lm x Fa F1 hybrids, generating either dihaploid Lm lines or Fa lines. Flow cytometry, a method for rapidly characterizing optical properties of cells and cell components within individuals, has been applied to identify the prevalence and timing of chimera formation in these Lm x Fa F1 hybrids through measurements of genome size estimation. Preliminary results indicate flow cytometry can clearly identify genomic sectors within nuclei extracted from leaf tissue, predict the size and frequency of the genomic sectors and can suggest the particular environmental parameters that enhance or reduce chimera formation. Due to the high throughput capabilities of flow cytometry, the method has also been effectively applied toward the rapid identification of both Lm or Fa dihaploid individuals, greatly reducing the need for standard root-tip chromosome squash methods.