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Shoot and root single cell sequencing reveals tissue- and daytime-specific transcriptome profiles

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Apelt,  Federico
Intercellular Macromolecular Transport, Department Köhler, Max Planck Institute of Molecular Plant Physiology, Max Planck Society;

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Mavrothalassiti,  E.
Intercellular Macromolecular Transport, Department Köhler, Max Planck Institute of Molecular Plant Physiology, Max Planck Society;

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Gupta,  S.
Intercellular Macromolecular Transport, Department Köhler, Max Planck Institute of Molecular Plant Physiology, Max Planck Society;

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Machin,  F.
Intercellular Macromolecular Transport, Department Köhler, Max Planck Institute of Molecular Plant Physiology, Max Planck Society;

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Annunziata,  Maria Grazia
System Regulation, Department Stitt, Max Planck Institute of Molecular Plant Physiology, Max Planck Society;

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Schindelasch,  D.
Intercellular Macromolecular Transport, Department Köhler, Max Planck Institute of Molecular Plant Physiology, Max Planck Society;

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Kragler,  F.
Intercellular Macromolecular Transport, Department Köhler, Max Planck Institute of Molecular Plant Physiology, Max Planck Society;

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Citation

Apelt, F., Mavrothalassiti, E., Gupta, S., Machin, F., Olas, J. J., Annunziata, M. G., et al. (2022). Shoot and root single cell sequencing reveals tissue- and daytime-specific transcriptome profiles. Plant Physiology, 188(2), 861-878. doi:10.1093/plphys/kiab537.


Cite as: https://hdl.handle.net/21.11116/0000-0009-8A1A-F
Abstract
Although several large-scale single-cell RNA sequencing (scRNAseq) studies addressing the root of Arabidopsis (Arabidopsis thaliana) have been published, there is still need for a de novo reference map for both root and especially above-ground cell types. As the plants’ transcriptome substantially changes throughout the day, shaped by the circadian clock, we performed scRNAseq on both Arabidopsis root and above-ground tissues at defined times of the day. For the root scRNAseq analysis, we used tissue-specific reporter lines grown on plates and harvested at the end of the day (ED). In addition, we submitted above-ground tissues from plants grown on soil at ED and end of the night to scRNAseq, which allowed us to identify common cell types/markers between root and shoot and uncover transcriptome changes to above-ground tissues depending on the time of the day. The dataset was also exploited beyond the traditional scRNAseq analysis to investigate non-annotated and di-cistronic transcripts. We experimentally confirmed the predicted presence of some of these transcripts and also addressed the potential function of a previously unidentified marker gene for dividing cells. In summary, this work provides insights into the spatial control of gene expression from nearly 70,000 cells of Arabidopsis for below- and whole above-ground tissue at single-cell resolution at defined time points.