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In This Article

  • Summary
  • Abstract
  • Introduction
  • Protocol
  • Representative Results
  • Discussion
  • Acknowledgements
  • Materials
  • References
  • Reprints and Permissions

Summary

Translating ribosome affinity purification (TRAP) offers the possibility to dissect developmental programs with minimal processing of organs and tissues. The protocol yields high-quality RNA from cells targeted with a green fluorescent protein (GFP)-labeled ribosomal subunit. Downstream analysis tools, such as qRT-PCR or RNA-seq, reveal tissue and cell type-specific expression profiles.

Abstract

In this article, we give hands-on instructions to obtain translatome data from different Arabidopsis thaliana root cell types via the translating ribosome affinity purification (TRAP) method and consecutive optimized low-input library preparation.

As starting material, we employ plant lines that express GFP-tagged ribosomal protein RPL18 in a cell type-specific manner by use of adequate promoters. Prior to immunopurification and RNA extraction, the tissue is snap frozen, which preserves tissue integrity and simultaneously allows execution of time series studies with high temporal resolution. Notably, cell wall structures remain intact, which is a major drawback in alternative procedures such as fluorescence-activated cell sorting-based approaches that rely on tissue protoplasting to isolate distinct cell populations. Additionally, no tissue fixation is necessary as in laser capture microdissection-based techniques, which allows high-quality RNA to be obtained.

However, sampling from subpopulations of cells and only isolating polysome-associated RNA severely limits RNA yields. It is, therefore, necessary to apply sufficiently sensitive library preparation methods for successful data acquisition by RNA-seq.

TRAP offers an ideal tool for plant research as many developmental processes involve cell wall-related and mechanical signaling pathways. The use of promoters to target specific cell populations is bridging the gap between organ and single-cell level that in turn suffer from little resolution or very high costs. Here, we apply TRAP to study cell-cell communication in lateral root formation.

Introduction

Driven by the increasing application of next-generation sequencing techniques, spatial resolution in developmental biology could be augmented. Contemporary studies aim at dissecting tissues down to specialized cell types, if not single-cell level1,2,3,4. To this end, a plethora of different methods has been devised over the last fifty years (see Figure 1A)5,6,7,8,9

Protocol

1. Cloning of transgene, transgenic line production and selection

  1. Clone the promoter of choice in the appropriate entry vector. Use a recombination-based cloning method (Table of Materials) and recombine the promoters in pDONRP4-P1r. Clone RPL18 (with affinity tag or fluorescent protein of choice) using recombination-based cloning in pDONRP1-P249.
  2. Combine the entry vector containing RPL18 with the promoter-containing entry vector in a two fragment re.......

Representative Results

For quality assessment, the above-mentioned procedure should be probed at several intermediate steps: expression pattern validation in planta, quality control of the isolated polysomal RNA as well as of the final libraries. qRT-PCR using known marker genes can, in addition, be performed to confirm the response to the treatment condition or to fine-tune the experimental conditions.

Confocal analysis of GFP signal distribu.......

Discussion

Verification of RPL18 localization pattern
Crucial to avoid misinterpretation of data from any TRAP experiment is the proper expression pattern of the tagged ribosomal subunit. Therefore, the incorporation of GFP as an epitope tag to RPL18 very elegantly allows verification of the desired expression pattern and consecutively, pulldown of the polysome fraction from the same tissue. More invasive approaches to assure proper promoter patterns are followed by Jiao and Mayerowitz 2010, which requires GU.......

Acknowledgements

We would like to thank Jean-Claude Walser of the Genetic Diversity Center Zurich for crucial expert advice in the early phase of this project. Work in the Vermeer lab was supported by an SNF Professorship grant (PP00P3_157524) and a R'EQUIP equipment grant (316030_164086) from the Swiss National Science Foundation (SNSF) awarded to JEMV.

....

Materials

NameCompanyCatalog NumberComments
Sterilization
bleach, 13%Sigma71696
beakerVWR214-1172/74/75
desiccator with porcelaine plate (DURAN)Sigma/MerckZ317454-1EA/Z317594-1EA
EtOH, p.a.Honeywell02860-1L
HCl, 37%Roth4625.1
Tween 20SigmaP9416
Plate growth + harvesting
MS salts, basal salt mixture, incl. MES bufferDuchefaM0254
agar plant for cell cultureApplichem/PanreacA2111.1000
DMSOSigmaD4540
forceptsRubis Switzerland5-SA model
KOHFluka60370
micropore/surgical tape3M1530-0
NAADuchefaN0903
petri dishes 120x120 mmGreiner bio-one688102
scalpelVWR/Swann-Morton233-5454
tissues, neutral, two-layeredany supplier of your choice
Immunoprecipitation
GFP-beads: gtma-100 GFP-Trap_MAChromoteke.g. gtma-100
Brij-35SigmaP1254-500G
centrifuge tubes (in accordance with centrifuge)Beckman Coulter357001
ChloramphenicolApplichemC0378-25G
cotton glovesVWR113-7355
Cycloheximide, HPLC gradeSigma01810-1G
DEPCVWRE174might have long delivery times
DTTFluka43815
EGTASigma3054.3
homogenizers DUALL 23KONTES GLASS CO (via VWR)SCERSP885450-0023 (set)SCERSP885451-0023 pestle only - SCERSP885452-0023 cylinder only; long delivery times
Igepal CA-360SigmaI3021-100ml
KClSigma60130
MgCl2 hexahydratRoth2189.2
mortar and pestleVWR470148-960 & 470019-978
PMSFRoche10 837 091 001
Polyoxyethylene-(10)-tridecylether/PTESigmaP2393-500G
RNase-free waterRothT143.3
RNAZapThermo FisherAM9780/AM9782for cleaning surfaces
Tris, >99.3%RothAE15.3
Triton X-100FlukaT8787-250ml
Tween 20SigmaP9416-100ml
RNA extraction
2-Propanol, p.a.Sigma33539-1L-GL-R
Chloroform, HPLC gradeScharlauCL02181000
EtOH, p.a.Honeywell02860-1L
low-retention microcentrifuge tubes, 1.5 mlEppendorf/SigmaZ666548-250EALoBind
RNase-free DNase setQiagen79254
RNeasy MiniElute Cleanup KitQiagen74204
TRIzol reagentThermoFisher/Ambion15596018
Library preparation
15/50 mL Tube Magnetic SeparatorAbraxisPN 472250
AMPure beadsBeckman CoulterA63881
Index Kit AIlluminaFC-131-2001
Index Kit DIlluminaFC-131-2004
neodymium magnetsAmazon/other6 x 1.5 mm range: N42 (NdFeB)
Nextera XT kitIlluminaFC-131-1024/1096https://emea.support.illumina.com/
PCR stripsThermoScientificAB-0266
SMARTer v4 kitTakara Bioscience634892https://www.takarabio.com/
BioanalyzerAgilent2100 Bioanalyzer Instrumentspecialized equipment for RNA/DNA quality control
TapestationAgilent4200 Tapestation Instrumentspecialized equipment for RNA/DNA quality control
Fragment AnalyzerAgilent5400 Fragment Analyzer Systemspecialized equipment for RNA/DNA quality control (high throughput)
LabChipPerkinElmerLabChip GX Touch Nucleic Acid Analyzerspecialized equipment for RNA/DNA quality control (high throughput)
Qubit 4 FluorometerThermoFisherQ33239specialized equipment for RNA/DNA concentration determination
qRT-PCR
GATA23Microsynthfwd: AGTGAGAATGAA
AGAAGAGAAGGG;
rev: GTGGCTGCGAAT
AATATGAATACC
GH3.3Microsynthfwd: CAAACCAATCCT
CCAAATGAC;
rev: ACTTATCCGCAA
CCCGACT
LBD29Microsynthfwd: TCTCCAACAACA
GGTTGTGAAT;
rev: AAGGAGCCTTAG
TAGTGTCTCCA
UBC21Microsynthfwd: TGCGACTCAGGG
AATCTTCT;
rev: TCATCCTTTCTT
AGGCATAGCG
SsoAdvanced Universal SYBR GreenBio-Rad#172-5270
iScript Adv cDNA KitBio-Rad#172-5038
miscellaneous
Falcon tubes 15 ml, CellstarGreiner bio-one188261
Falcon tubes 50 ml, CellstarGreiner bio-one210261
filter tips 1 mlAxygenTF-1000-R-S
filter tips 10 µlAxygenTF-10-R-S
filter tips 100 µlAxygenTF-100-R-S
filter tips 20 µlAxygenTF-20-R-S
filter tips 200 µlAxygenTF-200-R-S
microcentrifuge tubes 1.5 mlSARSTEDT72.690.001
Propidium iodideSigmaP4170-100MG
sequencing companyNovogeneen.novogene.com

References

  1. Van Verk, M. C., Hickman, R., Corné, M. J., Pieterse, M., Van Wees, S. C. RNA-Seq: Revelation Of The Messengers. Trends In Plant Science. 18 (4), 175-179 (2013).
  2. Libault, M., Pingault, L., Zogli, P., Schiefelbein, J. Plant Systems Biology At The Single-Cell Level....

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Ribosome Affinity Purification TRAPArabidopsis ThalianaRoot DevelopmentCell Type specificPolysome RNALow input RNALateral Root FormationCell cell CommunicationCell WallMechanical SignalingSeed SterilizationExogenous TreatmentNAA

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