Droplet-based microfluidic analysis and screening of single plant cells

Droplet-based microfluidics has been used to facilitate high-throughput analysis of individual prokaryote and mammalian cells. However, there is a scarcity of similar workflows applicable to rapid phenotyping of plant systems where phenotyping analyses typically are time-consuming and low-throughput...

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Veröffentlicht in:PloS one 2018-05, Vol.13 (5), p.e0196810-e0196810
Hauptverfasser: Yu, Ziyi, Boehm, Christian R, Hibberd, Julian M, Abell, Chris, Haseloff, Jim, Burgess, Steven J, Reyna-Llorens, Ivan
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container_issue 5
container_start_page e0196810
container_title PloS one
container_volume 13
creator Yu, Ziyi
Boehm, Christian R
Hibberd, Julian M
Abell, Chris
Haseloff, Jim
Burgess, Steven J
Reyna-Llorens, Ivan
description Droplet-based microfluidics has been used to facilitate high-throughput analysis of individual prokaryote and mammalian cells. However, there is a scarcity of similar workflows applicable to rapid phenotyping of plant systems where phenotyping analyses typically are time-consuming and low-throughput. We report on-chip encapsulation and analysis of protoplasts isolated from the emergent plant model Marchantia polymorpha at processing rates of >100,000 cells per hour. We use our microfluidic system to quantify the stochastic properties of a heat-inducible promoter across a population of transgenic protoplasts to demonstrate its potential for assessing gene expression activity in response to environmental conditions. We further demonstrate on-chip sorting of droplets containing YFP-expressing protoplasts from wild type cells using dielectrophoresis force. This work opens the door to droplet-based microfluidic analysis of plant cells for applications ranging from high-throughput characterisation of DNA parts to single-cell genomics to selection of rare plant phenotypes.
doi_str_mv 10.1371/journal.pone.0196810
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However, there is a scarcity of similar workflows applicable to rapid phenotyping of plant systems where phenotyping analyses typically are time-consuming and low-throughput. We report on-chip encapsulation and analysis of protoplasts isolated from the emergent plant model Marchantia polymorpha at processing rates of &gt;100,000 cells per hour. We use our microfluidic system to quantify the stochastic properties of a heat-inducible promoter across a population of transgenic protoplasts to demonstrate its potential for assessing gene expression activity in response to environmental conditions. We further demonstrate on-chip sorting of droplets containing YFP-expressing protoplasts from wild type cells using dielectrophoresis force. 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subjects Agrobacterium
Agrobacterium tumefaciens - genetics
Analysis
Bacterial Proteins - analysis
Bacterial Proteins - genetics
Biology and Life Sciences
Cell Separation - instrumentation
Cell Separation - methods
Cells (Biology)
Deoxyribonucleic acid
Dielectrophoresis
DNA
Drug Compounding
Engineering and Technology
Environmental conditions
Equipment Design
Gene expression
Gene Expression Regulation, Plant
Genes, Reporter
Genetic engineering
Genomes
Genomics - methods
High-Throughput Screening Assays - instrumentation
High-Throughput Screening Assays - methods
Hot Temperature
Lab-On-A-Chip Devices
Laboratories
Luminescent Proteins - analysis
Luminescent Proteins - genetics
Mammalian cells
Marchantia - chemistry
Marchantia - cytology
Marchantia - genetics
Marchantia polymorpha
Medical screening
Medicine and Health Sciences
Microfluidic Analytical Techniques - methods
Microfluidics
Microscopy, Fluorescence
Phenotypes
Phenotyping
Physical Sciences
Physiology
Plant biology
Plant cells
Plant sciences
Plants, Genetically Modified
Prokaryotes
Promoter Regions, Genetic
Protoplasts
Protoplasts - chemistry
Single-Cell Analysis - instrumentation
Single-Cell Analysis - methods
Stochastic Processes
Stochasticity
Synthetic biology
Transformation, Genetic
title Droplet-based microfluidic analysis and screening of single plant cells
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