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Marchant, D. B.

Publications and source records attributed to Marchant, D. B..

2 recordsLinked to original sources

FX-Cell: a method for single-cell RNA sequencing on difficult-to-digest and cryopreserved plant samples

Single-cell RNA sequencing (scRNA-seq) in plants requires the isolation of high-quality protoplasts-- cells devoid of cell walls. However, many plant tissues and organs are resistant to enzymatic digestion, posing a significant barrier to advancing single-cell multi-omics research in plants. Furthermore, for many field-grown crops, the lack of immediate laboratory access presents another major challenge for protoplast preparation. To address these limitations, we developed the FX-Cell method and its derivatives, FXcryo-Cell and cryoFX-Cell, to enable scRNA-seq with both difficult-to-digest and cryopreserved plant samples. By optimizing the fixation buffer and minimizing RNA degradation, our approach ensures efficient cell wall digestion at high temperatures while maintaining high-quality single cells, even after long-term storage at -80{degrees}C, and circumvents use of nuclei, which are not representative of the pool of translatable mRNAs. Using these methods, we successfully constructed high-quality cell atlases for rice tiller nodes, rhizomes of wild rice, and maize crown roots grown in field conditions. Moreover, these methods enable the accurate reconstruction of plant acute wounding responses at single-cell resolution. Collectively, these advancements expand the applicability of plant single-cell genomics across a wider range of species and tissues, paving the way for comprehensive Plant Cell Atlases for plant species.

plant biology↗

Quantitative cell release from plant tissues for single-cell genomics

Single-cell RNA-sequencing (scRNA-seq) can provide invaluable insight into cell development, cell type identification, and plant evolution. However, the resilience of the cell wall makes it difficult to dissociate plant tissues and release individual cells for single-cell analysis. Here, we show that plant organs can be rapidly and quantitatively dissociated into cells if fixed prior to enzymatic digestion. Fixation enables digestion at high temperatures at which enzymatic activity is optimal and stabilizes the plant cell cytoplasm, rendering cells resistant to mechanical shear force while maintaining high quality RNA. This protocol, FX-Cell, releases four to ten-fold more recoverable cells than optimized protoplasting methods applied to maize anthers or root tips with no cell type biases and can be readily applied to a variety of plant taxa and tissues with no optimization. FX-Cell and scRNA-seq analysis were applied to maize anthers for which 95% of the cells were dispersed and provided suitable scRNA-seq data for the identification of anther cell types with marker genes and well-understood biological functions, including rare meiocytes ([~]1% anther cells). In addition, the scRNA-seq data provided putative marker genes and gene ontology information for the identification of unknown cell types. FX-Cell also preserves the morphology of the isolated cells, permitting cell type identification without staining. Ultimately, FX-Cell can be applied to a range of plant species and tissues with minimal to no optimization paving the way for plant scRNA-seq analyses in non-model taxa and tissues.

plant biology↗