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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.
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.
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
1. Cloning of transgene, transgenic line production and selection
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.......
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.......
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.
....Name | Company | Catalog Number | Comments |
Sterilization | |||
bleach, 13% | Sigma | 71696 | |
beaker | VWR | 214-1172/74/75 | |
desiccator with porcelaine plate (DURAN) | Sigma/Merck | Z317454-1EA/Z317594-1EA | |
EtOH, p.a. | Honeywell | 02860-1L | |
HCl, 37% | Roth | 4625.1 | |
Tween 20 | Sigma | P9416 | |
Plate growth + harvesting | |||
MS salts, basal salt mixture, incl. MES buffer | Duchefa | M0254 | |
agar plant for cell culture | Applichem/Panreac | A2111.1000 | |
DMSO | Sigma | D4540 | |
forcepts | Rubis Switzerland | 5-SA model | |
KOH | Fluka | 60370 | |
micropore/surgical tape | 3M | 1530-0 | |
NAA | Duchefa | N0903 | |
petri dishes 120x120 mm | Greiner bio-one | 688102 | |
scalpel | VWR/Swann-Morton | 233-5454 | |
tissues, neutral, two-layered | any supplier of your choice | ||
Immunoprecipitation | |||
GFP-beads: gtma-100 GFP-Trap_MA | Chromotek | e.g. gtma-100 | |
Brij-35 | Sigma | P1254-500G | |
centrifuge tubes (in accordance with centrifuge) | Beckman Coulter | 357001 | |
Chloramphenicol | Applichem | C0378-25G | |
cotton gloves | VWR | 113-7355 | |
Cycloheximide, HPLC grade | Sigma | 01810-1G | |
DEPC | VWR | E174 | might have long delivery times |
DTT | Fluka | 43815 | |
EGTA | Sigma | 3054.3 | |
homogenizers DUALL 23 | KONTES GLASS CO (via VWR) | SCERSP885450-0023 (set) | SCERSP885451-0023 pestle only - SCERSP885452-0023 cylinder only; long delivery times |
Igepal CA-360 | Sigma | I3021-100ml | |
KCl | Sigma | 60130 | |
MgCl2 hexahydrat | Roth | 2189.2 | |
mortar and pestle | VWR | 470148-960 & 470019-978 | |
PMSF | Roche | 10 837 091 001 | |
Polyoxyethylene-(10)-tridecylether/PTE | Sigma | P2393-500G | |
RNase-free water | Roth | T143.3 | |
RNAZap | Thermo Fisher | AM9780/AM9782 | for cleaning surfaces |
Tris, >99.3% | Roth | AE15.3 | |
Triton X-100 | Fluka | T8787-250ml | |
Tween 20 | Sigma | P9416-100ml | |
RNA extraction | |||
2-Propanol, p.a. | Sigma | 33539-1L-GL-R | |
Chloroform, HPLC grade | Scharlau | CL02181000 | |
EtOH, p.a. | Honeywell | 02860-1L | |
low-retention microcentrifuge tubes, 1.5 ml | Eppendorf/Sigma | Z666548-250EA | LoBind |
RNase-free DNase set | Qiagen | 79254 | |
RNeasy MiniElute Cleanup Kit | Qiagen | 74204 | |
TRIzol reagent | ThermoFisher/Ambion | 15596018 | |
Library preparation | |||
15/50 mL Tube Magnetic Separator | Abraxis | PN 472250 | |
AMPure beads | Beckman Coulter | A63881 | |
Index Kit A | Illumina | FC-131-2001 | |
Index Kit D | Illumina | FC-131-2004 | |
neodymium magnets | Amazon/other | 6 x 1.5 mm range: N42 (NdFeB) | |
Nextera XT kit | Illumina | FC-131-1024/1096 | https://emea.support.illumina.com/ |
PCR strips | ThermoScientific | AB-0266 | |
SMARTer v4 kit | Takara Bioscience | 634892 | https://www.takarabio.com/ |
Bioanalyzer | Agilent | 2100 Bioanalyzer Instrument | specialized equipment for RNA/DNA quality control |
Tapestation | Agilent | 4200 Tapestation Instrument | specialized equipment for RNA/DNA quality control |
Fragment Analyzer | Agilent | 5400 Fragment Analyzer System | specialized equipment for RNA/DNA quality control (high throughput) |
LabChip | PerkinElmer | LabChip GX Touch Nucleic Acid Analyzer | specialized equipment for RNA/DNA quality control (high throughput) |
Qubit 4 Fluorometer | ThermoFisher | Q33239 | specialized equipment for RNA/DNA concentration determination |
qRT-PCR | |||
GATA23 | Microsynth | fwd: AGTGAGAATGAA AGAAGAGAAGGG; rev: GTGGCTGCGAAT AATATGAATACC | |
GH3.3 | Microsynth | fwd: CAAACCAATCCT CCAAATGAC; rev: ACTTATCCGCAA CCCGACT | |
LBD29 | Microsynth | fwd: TCTCCAACAACA GGTTGTGAAT; rev: AAGGAGCCTTAG TAGTGTCTCCA | |
UBC21 | Microsynth | fwd: TGCGACTCAGGG AATCTTCT; rev: TCATCCTTTCTT AGGCATAGCG | |
SsoAdvanced Universal SYBR Green | Bio-Rad | #172-5270 | |
iScript Adv cDNA Kit | Bio-Rad | #172-5038 | |
miscellaneous | |||
Falcon tubes 15 ml, Cellstar | Greiner bio-one | 188261 | |
Falcon tubes 50 ml, Cellstar | Greiner bio-one | 210261 | |
filter tips 1 ml | Axygen | TF-1000-R-S | |
filter tips 10 µl | Axygen | TF-10-R-S | |
filter tips 100 µl | Axygen | TF-100-R-S | |
filter tips 20 µl | Axygen | TF-20-R-S | |
filter tips 200 µl | Axygen | TF-200-R-S | |
microcentrifuge tubes 1.5 ml | SARSTEDT | 72.690.001 | |
Propidium iodide | Sigma | P4170-100MG | |
sequencing company | Novogene | en.novogene.com |
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