Method Article

Isolation of Active Caenorhabditis elegans Nuclear Extract and Reconstitution for In Vitro Transcription

DOI:

10.3791/62723

⸱

August 11th, 2021

In This Article

Summary

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Here, we describe a detailed protocol for isolating active nuclear extract from larval stage 4 C. elegans and visualizing transcription activity in an in vitro system.

Abstract

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Caenorhabditis elegans has been an important model system for biological research since it was introduced in 1963. However, C. elegans has not been fully utilized in the biochemical study of biological reactions using its nuclear extracts such as in vitro transcription and DNA replication. A significant hurdle for using C. elegans in biochemical studies is disrupting the nematode's thick outer cuticle without sacrificing the activity of the nuclear extract. While several methods are used to break the cuticle, such as Dounce homogenization or sonication, they often lead to protein instability. There are no established protocols for isolating active nuclear proteins from larva or adult C. elegans for in vitro reactions. Here, the protocol describes in detail the homogenization of larval stage 4 C. elegans using a Balch homogenizer. The Balch homogenizer uses pressure to slowly force the animals through a narrow gap breaking the cuticle in the process. The uniform design and precise machining of the Balch homogenizer allow for consistent grinding of animals between experiments. Fractionating the homogenate obtained from the Balch homogenizer yields functionally active nuclear extract that can be used in an in vitro method for assaying transcription activity of C. elegans.

Introduction

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The small, free-living nematode Caenorhabditis elegans is a simple yet powerful model organism for addressing a wide range of biological questions. Since its introduction in 1963, the nematodes have been invaluable to answering questions in neurobiology, metabolism, aging, development, immunity, and genetics1. Some of the animal's many characteristics that make it an ideal model organism include short generation time, the effectiveness of RNA interference, transparent body, and the completed maps of both its cellular lineage and nervous system.

While the nematode's contributions to science are vast, ....

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Protocol

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1. Media preparations

  1. Prepare sterile lysogeny broth (LB) agar plates and liquid media following the manufacturer's instructions.
  2. Streak Escherichia coli (E. coli) strain OP50 on a LB agar plate. Incubate the bacteria streak at 37 °C overnight.
  3. Store the E. coli OP50 streak plate at 4 °C after incubation. The E. coli OP50 plate can safely be stored at 4 °C for 2 weeks if wrapped in parafilm to prevent moisture loss.
  4. Prepare 2 L of Nematode Growth Media (NGM) using the recipe in Table 1.
    NOTE: Nystatin is optional. Nystatin helps prevent mold, a....

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Results

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Following the outlined steps should yield functional nuclear extract (Figure 1), deviation in the grinding or wash steps can lead to poor activity or low yields. If functional C. elegans nuclear extract is obtained, it will transcribe the region downstream of the CMV promoter on the DNA template when added to the previously described in vitro assay. The resulting RNA transcript can be purified from the nuclear proteins and DNA template usin.......

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Discussion

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C. elegans is an appealing model organism to study the eukaryotic transcription system because of its low-cost maintenance and the ease of genetic manipulation. Here a protocol for consistent isolation of functionally active nuclear extract from L4 C. elegans is described. Although this protocol focused on visualizing transcription activity, the cDNA produced post-transcriptionally can be quantified using RT-qPCR to obtain a more precise measurement of the transcription activity8.......

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Disclosures

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The authors have no competing interests to disclose.

Acknowledgements

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This work was supported by an NIH MIRA grant (R35GM124678 to J. S.).

....

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Materials

List of materials used in this article
NameCompanyCatalog NumberComments
Consumables and reagents
0.2 mL 8-Strip Tubes & Flat Strip Caps, ClearGenesee Scientific 24-706
0.2 mL Individual PCR tubesGenesee Scientific 24-153G
1.7 mL sterile microtubesGenesee Scientific24-282S
100% absolute molecular grade ethanolFisher Scientific BP2818
100% ethanol, KoptecDecon Labs V1001
10 mL serological pipetVWR international 89130-898
150 mm petri platesTritech Research T3325
15 mL conical centrifuge tubesGenesee Scientific 28-103
20 mL plastic syringesFisher Scientific14955460
2 mL Norm-Ject syringesHenke-Sass Wolf GmbH4020
500 mL vacuum filter cup 0.22 µm PES, Stericup Millipore Express PlusMillipore SigmaSCGPU10RE
50 mL conical centrifuge tubesThermoFisher Scientific339652
50 mL serological pipetVWR international 89130-902
5 mL serological pipetVWR international 89130-896
Agar, CriterionVWR International C7432
AgaroseDenville Scientific CA3510-6
Alcohol proof markerVWR International 52877-310
Bacto peptoneVWR International 90000-264
Caenorhabditis elegansCGCN2
Calcium dichlorideMillipore Sigma C4901
CholesterolMillipore Sigma C8667
Control DNA temple cloning primers, Forward 5’- ctc atg ttt gac agc tta tcg atc cgg gc -3’
Control DNA temple cloning primers, Forward 5’- aca gga cgg gtg tgg tcg cca tga t -3’
Deionized water
DithiothreitolInvitrogen 15508-013
DNA gel stain, SYBR safeInvitrogen S33102
DNA ladder mix, O’gene rulerFisher Scientific SM1173
DNA Loading Dye, 6x TriTrackFisher Scientific FERR1161
DNase, Baseline-ZEROLucigen DB0715K
Dry ice
Escherichia coli OP50 strainCGCOP50
Glacial acetic acidFisher Scientific A38
GlycerolMillipore Sigma G6279
HeLa nuclear extract in vitro transcription system, HeLaScribePromega E3110
Hepes Solution, 1 M GibcoMillipore Sigma15630080
Hydrochloric acid 37%Millipore Sigma P0662
Hypochlorite bleachClorox
LB BrothMillipore Sigma L3022
Magnesium dichlorideMillipore Sigma M8266
Magnesium SulfateMillipore Sigma M7506
Medium weigh dishesFisher Scientific 02-202-101
microscope slides, Vista visionVWR International16004-368
molecular grade water, HypureHyclone Laboratories SH30538
NystatinMillipore Sigma N1638
PCR system, FailSafe with premix ALucigen FS99100
Potassium chlorideMillipore Sigma P39111
Potassium phosphate dibasicMillipore Sigma P3786
Potassium phosphate monobasicMillipore Sigma P0662
Protease inhibitor, Halt single use cocktail 100xThermoFisher Scientific78430
protein assay kit, QubitThermoFisher Scientific Q33211
reverse transcription kit, SensiscriptQiagen205211
RNA extraction kit RNeasy micro kitQiagen74004
RNase InhibitorApplied Biosystems N8080119
Sodium ChlorideVWR International BDH9286-12KG
Sodium hydroxideMillipore Sigma 1-09137
Sterile syringe filter with 0.2 µm Polyethersulfone membraneVWR international28145-501
SucroseVWR International 200-334-9
transcription primers, Forward 5’- gcc ggg cct ctt gcg gga tat -3’
transcription primers, Reverse 5’- cgg cca aag cgg tcg gac agt-3’
Tris-BaseFisher Scientific BP152
Tween20Millipore Sigma P2287
Equipment
-20 °C incubatorThermoFisher Scientific
20 °C incubatorThermoFisher Scientific
37 °C incubatorForma Scientific
4 °C refrigeratorThermoFisher Scientific
-80 °C freezerEppendorf
AutoclaveSanyo
Balch homogenizer, isobiotec cell homogenizerIsobiotec
Benchtop VortexerFisher Scientific2215365
Centrifuge, Eppendorf 5418 REppendorf5401000013
Centrifuge, VWR Clinical 50VWR International82013-800
Dissection microscope, Leica M80Leica Microsystems
Fluorometer, Qubit 2.0InvitrogenQ32866
Gel imaging system, iBright FL1500ThermoFisher Scientific A44241
Gel systemThermoFisher Scientific
Heat blockVWR International12621-048
Microcentrifuges, Eppendorf 5424Eppendorf22620401
PIPETBOY acu 2Integra155017
Pipette L-1000 XLS+, Pipet-Lite LTSRainin17014382
Pipette L-10 XLS+, Pipet-Lite LTSRainin17014388
Pipette L-200 XLS+, Pipet-Lite LTSRainin17014391
Pipette L-20 XLS+, Pipet-Lite LTSRainin17014392
Rocking platformVWR International
Thermocycler, Eppendorf Mastercycler ProEppendorf950030010

References

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  1. Corsi, A. K., Wightman, B., Chalfie, M. A Transparent window into biology: A on Caenorhabditis elegans. Genetics. 200 (2), 387-407 (2015).
  2. Blackwell, T. K., Walker, A. K. Transcription mechanisms. WormBook: The Online Review of C. elegans Biology. , Pasadena, CA. 1-16 (2006).
  3. ....

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Tags

Caenorhabditis ElegansNuclear ExtractIn Vitro TranscriptionBalch HomogenizerNuclear Protein IsolationLarval Stage FourHypotonic BufferHypertonic BufferRNA TranscriptionProtein Quantification

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