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Method Article

Isolate Cell-Type-Specific RNAs from Snap-Frozen Heterogeneous Tissue Samples without Cell Sorting

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DOI:

10.3791/63143

December 8th, 2021

In This Article

Summary

This protocol aims to isolate cell-type-specific translating ribosomal mRNAs using the NuTRAP mouse model.

Abstract

Cellular heterogeneity poses challenges to understanding the function of complex tissues at a transcriptome level. Using cell-type-specific RNAs avoids potential pitfalls caused by the heterogeneity of tissues and unleashes the powerful transcriptome analysis. The protocol described here demonstrates how to use the Translating Ribosome Affinity Purification (TRAP) method to isolate ribosome-bound RNAs from a small amount of EGFP-expressing cells in a complex tissue without cell sorting. This protocol is suitable for isolating cell-type-specific RNAs using the recently available NuTRAP mouse model and could also be used to isolate RNAs from any EGFP-expressing cells.

Introduction

High-throughput approaches, including RNA sequencing (RNA-seq) and microarray, have made it possible to interrogate gene expression profiles at the genome-wide level. For complex tissues such as the heart, brain, and testis, the cell-type-specific data will provide more details comparing the use of RNAs from the whole tissue1,2,3. To overcome the impact of cellular heterogeneity, the Translating Ribosome Affinity Purification (TRAP) method has been developed since early 2010s4. TRAP is able to isolate ribosome-bound RNAs from specific cell types withou....

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Protocol

All performed animal experiments followed the protocols approved by the Institutional Animal Care and Use Committees (IACUC) at Auburn University.

NOTE: The following protocol uses one testis (about 100 mg) at P28 from Gli1-CreERT2; NuTRAP mice (Mus musculus). Volumes of reagents may need to be adjusted based on the types of samples and the number of tissues.

1. Tissue collection

  1. Euthanize the mice using a CO2 chamber, sanitize the abdomen surface with 70% ethanol.
  2. Open the lower abdomen with scissors and remove the testes. Use li....

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Results

Gli1-CreERT2 mouse (Jackson Lab Stock Number: 007913) were first crossed with the NuTRAP reporter mouse (Jackson Lab Stock Number: 029899) to generate double-mutant mice. Mice carrying both genetically engineered gene alleles (i.e., Gli1-CreERT2 and NuTRAP) were injected with tamoxifen once a day, every other day, for three injections. Tissue samples were collected on the 7th day after the 1st day of the injection. Immunofluorescence analysis showed t.......

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Discussion

The usefulness of the whole-tissue transcriptome analysis could be dampened, especially when studying complex heterogeneous tissues. How to obtain cell-type-specific RNAs becomes an urgent need to unleash the powerful RNA-seq technique. The isolation of cell-type-specific RNAs usually relies on the collection of a specific type of cells using micromanipulation, fluorescent-activated cell sorting (FACS), or laser capture microdissection (LCM)18. Other modern high-throughput single-cell collection m.......

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Disclosures

The authors declare no conflict of interest.

Acknowledgements

This work was partially supported by NIH R00HD082686. We thank the Endocrine Society Summer Research Fellowship to H.S.Z. We also thank Dr. Yuan Kang for breeding and maintaining the mouse colony.

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Materials

List of materials used in this article
NameCompanyCatalog NumberComments
ActbeurofinsqPCR primersATGGAGGGGAATACAGCCC / TTCTTTGCAGCTCCTTCGTT (forward primer/reverse primer)
BioanalyzerAgilent2100 Bioanalyzer Instrument
cOmplete Mini EDTA-free Protease Inhibitor CocktailMillipore11836170001
cycloheximideMillipore239764-100MG
Cyp11a1eurofinsqPCR primersCTGCCTCCAGACTTCTTTCG / TTCTTGAAGGGCAGCTTGTT (forward primer/reverse primer)
dNTPThermo Fisher ScientificR0191
DTT, DithiothreitolThermo Fisher ScientificP2325
DynaMag-2 magnetThermo Fisher Scientific12321D
Falcon tubes 15 mLVWR89039-666
GFP antibodyAbcamab290
Glass grinder setDWK Life Sciences357542
heparinBEANTOWN CHEMICAL139975-250MG
Hsd3beurofinsqPCR primersGACAGGAGCAGGAGGGTTTGTG / CACTGGGCATCCAGAATGTCTC (forward primer/reverse primer)
KClBiosciencesR005
MgCl2BiosciencesR004
Microcentrifuge tubes 2 mLThermo Fisher Scientific02-707-354
Mouse Clariom S Assay microarraysThermo Fisher ScientificMicroarray service
NP-40Millipore492018-50 Ml
oligo (dT)20Invitrogen18418020
PicoPure RNA Isolation KitThermo Fisher ScientificKIT0204
Protein G DynabeadThermo Fisher Scientific10003D
RNase-free watergrowcellsNUPW-0500
RNaseOUT Recombinant Ribonuclease InhibitorThermo Fisher Scientific10777019
Sox9eurofinsqPCR primersTGAAGAACGGACAAGCGGAG / CTGAGATTGCCCAGAGTGCT (forward primer/reverse primer
Superscript IV reverse transcriptaseInvitrogen18090050
SYBR Green PCR Master MixThermo Fisher Scientific4309155
Sycp3eurofinsqPCR primersGAATGTGTTGCAGCAGTGGGA /GAACTGCTCGTGTATCTGTTTGA (forward primer/reverse primer)
TrisAlfa AesarJ62848

References

  1. Yang, K. C., et al. Deep RNA sequencing reveals dynamic regulation of myocardial noncoding RNAs in failing human heart and remodeling with mechanical circulatory support. Circulation. 129 (9), 1009-1021 (2014).
  2. Soumillon, M., et al.

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Tags

Cell Type Specific RNATranslating Ribosome Affinity PurificationRibosome Bound RNAEGFP Expressing CellsNuTRAP Mouse ModelRNA PurificationMagnetic Bead IsolationMicroarray AnalysisQuantitative RT PCRTissue Homogenization