Search bioRxiv⌕ Search

bioRxiv · 10.1101/2024.02.14.580322

A flow cytometry protocol for accurate and precise measurement of plant genome size using frozen material

Abstract

Flow cytometry is a technique widely applied to infer the ploidy and genome size of plant nuclei. The conventional approach of sample preparation, reliant on fresh plant material to release intact nuclei, requires protocol optimisation for application to many species. The approach often results in poor yields of nuclei, impeding the accurate measurement of genome size and confines the optimal resource allocation and efficiency in genome sequencing which relies on genome size estimation. Here, we present a novel method using frozen plant material that facilitates the release of intact nuclei for genome size estimation. Genome estimates from frozen material are similar to those from fresh material. Accurate and precise estimates can be made by complementing the fluorescence of frozen nuclei with histogram modelling and debris compensation algorithms. This method of nuclei isolation from frozen plant material for flow cytometry-based genome size estimations has special value in estimating the genome size of samples collected and frozen for use in plant genome sequencing. Plant material can be conveniently stored, resampled, and used for DNA or RNA extractions. HighlightFrozen leaf material can be used to isolate nuclei for the accurate estimation of genome size The method proved suitable for difficult samples and did not require specific optimization. The method was especially useful where plant material could not be immediately processed through flow cytometry and allowed the same sample to be used for genomes size estimation and genome sequencing.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Soni, A., Constantin, L., Furtado, A., Henry, R.. 2024-02-16. A flow cytometry protocol for accurate and precise measurement of plant genome size using frozen material. https://doi.org/10.1101/2024.02.14.580322

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

Integrative Nanopore and Illumina sequencing reveals age-associated tRNA modification and CCA-tail dynamics in yeast

Aging is characterized by a progressive loss of proteostasis. Transfer RNAs (tRNAs) are essential regulators of translation, yet their dynamics during aging remain poorly understood due to challenges in sequencing highly modified RNAs. Here we present a benchmarked Nanopore direct RNA sequencing (RNA004 chemistry) resource that profiles the Saccharomyces cerevisiae tRNAome during replicative aging at single-molecule resolution. Using in vitro transcribed tRNA controls, we establish modification detection thresholds and validate key findings with orthogonal Illumina sequencing. While overall tRNA abundance remains largely stable, our resource reveals age-associated terminal A cleavage at the 3' CCA tail of mature tRNAs, targeted T-loop and anticodon modification changes, and single-molecule evidence of modification co-occurrence. This dataset provides a resource for exploring tRNA regulation, translation fidelity, and longevity.

genomics↗

A hydrogen-producing mitochondrion in an anaerobic eukaryotrophic rhizarian

Diverse eukaryotes thrive under low oxygen conditions, in part through highly modified mitochondrion-related organelles (MROs) that use alternate metabolic pathways to support ATP production and cofactor recycling. Anaerobic lifestyles have evolved repeatedly across the eukaryotic tree of life, each providing an independent opportunity to understand how eukaryotes adapt to life in low oxygen conditions. Here, we use single-cell transcriptomics to reconstruct the MRO metabolism of PCE SSF, a benthic eukaryotrophic flagellate and the first cultivated representative of Novel Clade 12 (NC12; Rhizaria), an independently anaerobic rhizarian lineage. PCE SSF possesses an anaerobic hydrogen-producing mitochondrion capable of hydrogenosome-type substrate-level phosphorylation. It also retains a nearly complete but likely branched tricarboxylic acid pathway that lacks citrate synthase and malate dehydrogenase. The function of citrate synthase may instead be fulfilled by the typically cytosolic ATP citrate lyase, previously reported in this context only in the anaerobic cercozoan, Brevimastigomonas motovehiculus. Unlike B. motovehiculus, however, PCE SSF retains only Complex II and the NuoE/NuoF subunits of the electron transport chain and lacks a mitochondrial genome. Together, these features indicate an atypical and reduced mitochondrial metabolism, highlighting the diversity of evolutionary solutions to anaerobic energy metabolism in eukaryotes.

genomics↗

Targeted CRISPRi screening reveals unexpected resilience across the RNA polymerase III transcriptome

Increased RNA polymerase III (Pol III) activity and tRNA abundance are widely linked to cancer cell growth, yet the functional requirement for individual Pol III genes and core components remains unclear, in part due to the difficulty of achieving gene-specific perturbation of highly conserved loci. Here, we developed an inducible CRISPR interference platform and a custom single-guide RNA (sgRNA) library enabling gene-specific targeting of Pol III-transcribed genes and Pol III machinery. Genome-wide screening identified several Pol III dependencies in diploid fibroblasts and HEK293T cells, including multiple initiator methionine tRNA genes among the strongest fitness dependencies. Unexpectedly, glioblastoma models remained largely insensitive to repression of both individual Pol III genes and core Pol III components, despite efficient target repression. These findings establish a general strategy for gene-specific interrogation of conserved Pol III genes and indicate that glioblastoma models tolerate extensive perturbation of Pol III genes and machinery.

genomics↗