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The feasibility and effectiveness of high-throughput scRNA-seq methods herald a single-cell era in plant research. Presented here is a robust and complete procedure for isolating specific Arabidopsis thaliana root cell types and subsequent transcriptome library construction and analysis.
In multicellular organisms, developmental programming and environmental responses can be highly divergent in different cell types or even within cells, which is known as cellular heterogeneity. In recent years, single-cell and cell-type isolation combined with next-generation sequencing (NGS) techniques have become important tools for studying biological processes at single-cell resolution. However, isolating plant cells is relatively more difficult due to the presence of plant cell walls, which limits the application of single-cell approaches in plants. This protocol describes a robust procedure for fluorescence-activated cell sorting (FACS)-based single-cell and cell-type isolation with plant cells, which is suitable for downstream multi-omics analysis and other studies. Using Arabidopsis root fluorescent marker lines, we demonstrate how particular cell types, such as xylem-pole pericycle cells, lateral root initial cells, lateral root cap cells, cortex cells, and endodermal cells, are isolated. Furthermore, an effective downstream transcriptome analysis method using Smart-seq2 is also provided. The cell isolation method and transcriptome analysis techniques can be adapted to other cell types and plant species and have broad application potential in plant science.
Cells are the fundamental unit of all living organisms and perform structural and physiological functions. Although the cells in multicellular organisms show apparent synchronicity, cells of different types and individual cells present differences in their transcriptomes during development and environmental responses. High-throughput single-cell RNA sequencing (scRNA-seq) provides unprecedented power for understanding cellular heterogeneity. Applying scRNA-seq in plant sciences has contributed to successfully constructing a plant cell atlas1, has been used to identify rare cellular taxa in plant tissues2, has provided in....
The following protocol has been optimized for A. thaliana wild-type (WT) seeds with no fluorescence and fluorescent marker lines for the following root cell types: xylem-pole pericycle cells (J0121), lateral root initial cells, lateral root cap cells (J3411), endodermis and cortex cells (J0571) (Figure 1A). All the marker lines were obtained from a commercial source (see Table of Materials), except for the lateral root initiation cell marker line, which was generated by introducing a GATA23 promoter-driven GFP construct into a wild-type Arabidopsis plant following a previously published report<....
Protoplast isolation
This protocol is effective for the protoplast sorting of fluorescent A. thaliana root marker lines. These markers lines have been developed by the fusion of fluorescent proteins with genes expressed specifically in target cell types, or using enhancer trap lines (Figure 1). Numerous tissues and organs have been dissected into cell types expressing specific fluorescent markers in model plants and crops.
F.......
The Smart-seq2-based protocol can generate reliable sequencing libraries from several hundreds of cells8. The quality of the starting material is essential for the accuracy of the transcriptome analysis. FACS is a powerful tool for preparing cells of interest, but this procedure, especially the protoplasting step, must be optimized for plant applications. Laser capture microdissection (LCM) or manual dissected cells can also be used as input25,2.......
The authors have nothing to disclose.
We set up this protocol in the single-cell multi-omics facility of the School of Agriculture and Biology, Shanghai Jiao Tong University, and were supported by the National Natural Science Foundation of China (Grant No. 32070608), the Shanghai Pujiang Program (Grant No. 20PJ1405800), and Shanghai Jiao Tong University (Grant Nos. Agri-X20200202, 2019TPB05).
....Name | Company | Catalog Number | Comments |
0.22 µm strainer | Sorfa | 622110 | |
Agar | Yeasen | 70101ES76 | |
Agilent fragment analyzer | Aglient | Aglient 5200 | |
Agilent high-sensitivity DNA kit | Aglient | DNF-474-0500 | |
Ampure XP beads | BECKMAN | A63881 | |
Betaine | yuanye | S18046-100g | |
Bleach | Mr Muscle | FnBn83BK | 20% (v/v) bleach |
BSA | sigma | 9048-46-8 | |
CaCl2 | yuanye | S24109-500g | |
Cellulase R10 | Yakult (Japan) | 9012-54-8 | |
Cellulase RS | Yakult (Japan) | 9012-54-8 | |
Centrifuge tube (1.5 mL) | Eppendolf | 30121589 | |
DNase, RNase, DNA and RNA Away Surface Decontaminants | Beyotime | R0127 | |
dNTPs (10 mM) | NEB | N0447S | |
DTT (0.1 M) | invitrogen | 18090050 | |
Ethanol | Sinopharm Chemical Reagent Co., Ltd | 100092680 | |
FACS | BD FACS Melody | BD-65745 | |
FACS | Sony | SH800S | |
Filter tip (1000 µL) | Thermo Scientific | TF112-1000-Q | |
Filter tip (200 µL) | Thermo Scientific | TF140-200-Q | |
Filter tip (10 µL) | Thermo Scientific | TF104-10-Q | |
Filter tip (100 µL) | Thermo Scientific | TF113-100-Q | |
Fluorescent microscope | Nikon | Eclipse Ni-E | |
Four-Dimensional Rotating Mixer | Kylin -Bell | BE-1100 | |
Hemicellulase | sigma | 9025-56-3 | |
IS PCR primer | 5'-AAGCAGTGGTATCAACGCAGAG T-3' | ||
KAPA HiFi HotStart ReadyMix(2X) | Roche | 7958935001 | |
KCl | Sinopharm Chemical Reagent Co., Ltd | 7447-40-7 | |
Macerozyme R10 | Yakult (Japan) | 9032-75-1 | |
Magnetic separation stand | invitrogen | 12321D | |
Mannitol | aladdin | 69-65-8 | |
MES | aladdin | 145224948 | |
MgCl2 | yuanye | R21455-500ml | |
Microcentrifuges | Eppendorf | Centrifuge 5425 | |
Micro-mini-centrifuge | Titan | Timi-10k | |
MS | Phytotech | M519 | |
Nextera XT DNA Library Preparation Kit | illumina | FC-131-1024 | |
oligo-dT30VN primer | 5'-AAGCAGTGGTATCAACGCAGAG TACTTTTTTTTTTTTTTTTTTTTTTT TTTTTTTTTTVN-3' | ||
PCR instrument | Thermal cycler | A24811 | |
Pectolyase | Yakult (Japan) | 9033-35-6 | |
Plant marker lines | Nottingham Arabidopsis Stock Centre (NASC) | ||
Qubit 1x dsDNA HS Assay Kit | invitrogen | Q33231 | |
Qubit 2.0 fluorometer | invitrogen | Q32866 | |
RNase inhibitor | Thermo Scientific | EO0382 | |
RNase-free water | invitrogen | 10977023 | |
Solution A | 400 mM mannitol, 0.05 % BSA , 20 mM MES (pH5.7), 10 mM CaCl2, 20 mM KCl | ||
Solution B | 1 % (w/v)cellulase R10, 1 % (w/v) cellulase RS, 1 % (w/v)hemicellulase, 0.5 % (w/v)pectolyase and 1 % (w/v) Macerozyme R10 of in a fresh aliquot of solution A | ||
Sterile pestle | BIOTREAT | 453463 | |
Strainer (40 µm ) | Sorfa | 251100 | |
Superscript enzyme (200 U/µL) | invitrogen | 18090050 | |
SuperScript VI buffer (5x) | invitrogen | 18090050 | |
T0est tube (5 mL) | BD Falcon | 352052 | |
Thin-walled PCR tubes with caps (0.5 mL) | AXYGEN | PCR-05-C | |
Triton X-100 | Sangon Biotech | A600198-0500 | |
TSO primer | 5'-AAGCAGTGGTATCAACGCAGAG TACATrGrG+G-3' | ||
Vortex | Titan | VM-T2 |
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