Method Article

Functional Cloning Using a Xenopus Oocyte Expression System

DOI:

10.3791/53518

January 30th, 2016

In This Article

Summary

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We describe a Xenopus oocyte and animal cap system for the expression cloning of genes capable of inducing a response in competent ectoderm, and discuss techniques for the subsequent analysis of such genes. This system is useful in the functional identification of a wide range of gene products.

Abstract

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Identification of genes responsible for embryonic induction poses a number of challenges; to name a few, secreted molecules of interest may be low in abundance, may not be secreted but tethered to the signaling cell(s), or may require the presence of binding partners or upstream regulatory molecules. Thus in a search for gene products capable of eliciting an early lens-inductive response in competent ectoderm, we utilized an expression cloning system that would allow identification of paracrine or juxtacrine factors as well as transcriptional or other regulatory proteins. Pools of mRNA were injected into Xenopus oocytes, and responding tissue placed directly on the oocytes and co-cultured. Following functional cloning of ldb1 from a neural plate stage cDNA library based on its ability to elicit the expression of the early lens placode marker foxe3 in lens-competent animal cap ectoderm, we characterized the mRNA expression pattern, and assayed developmental progression following overexpression or knockdown of ldb1. This system is suitable in a very wide variety of contexts where identification of an inducer or its upstream regulatory molecules is sought using a functional response in competent tissue.

Introduction

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Forward genetic approaches to identify genes of interest through their function or loss-of-function1,2 are an integral part of understanding complex patterning events in development. Coupled with powerful reverse genetic techniques available to an ever-widening array of systems and researchers3-5, it is now possible to identify genes with a key functional role in a pathway and then elucidate that function at the cellular level and in interaction with other gene products. One approach to functionally identifying genes of interest that has yielded many key findings in the past is expression cloning6,7.

Our r....

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Protocol

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All experimental procedures were approved by the University of Virginia Institutional Animal Care and Use Committee.

Note: Figure 1 shows a schematic overview of the experimental procedures.

1. Preparation of Oocytes

  1. Pre-prime X. laevis females with 150 U of Pregnant Mare Serum Gonadotropin (PMSG) approximately one week in advance of oocyte isolation. Inject 1 ml 150 U/ml PMSG into dorsal lymph sac with 1 cc sterile syringe with 29 G needle.
  2. Prepare solutions for oocyte injection and oocyte-animal cap assay.
    1. Prepare Ca++/Mg

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Results

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In response to expression of mRNA injected into oocytes, responding animal cap tissue was assayed for expression of otx2 by in situ hybridization (Figure 2 and Table 1); otx2 is expressed in the presumptive lens ectoderm (PLE) from neural tube closure through lens placode thickening19. However, since otx2 is also expressed in the anterior neural ectoderm as well as non-neural head ectoderm outside the PLE, it is associated wi.......

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Discussion

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The method described here for the functional cloning of genes capable of inducing a response in competent ectoderm can be used to identify a wide range of gene products. This method expands upon past work by combining tissue-inducing assays with expression cloning techniques. We utilize the metabolic pathways of the Xenopus oocyte as a source of production of inducing factors, directly or indirectly, following RNA injection. This, in combination with the use of established methods for cloning a gene of interest<.......

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Disclosures

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The authors declare that they have no competing financial interests.

Acknowledgements

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This work was supported by a Professional Development Grant to C.Z.P. from the Shepherd University Foundation. The authors wish to thank Brett Zirkle and Malia Deshotel for helpful discussions on the protocols, and Dr. Carol Hurney for generous assistance.

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Materials

List of materials used in this article
NameCompanyCatalog NumberComments
12/101 AntibodyDevelopmental Studies Hybridoma Bank12/101Monoclonal antibody for detection of muscle tissue
20x SSC BufferSigmaS6639for ISH
Acetic anhydrideSigmaA6404for ISH
Anti-Dig-APRoche11093274910for ISH
Aurum Plasmid Mini KitBio-Rad732-6400Plasmid DNA purification
Blocking ReagentRoche11096176001for ISH
BM PurpleRoche11442074001for ISH
Boekel Hybridization OvenFisher Scientific13-245-121for ISH
Bouin's SolutionSigmaHT10132for ISH
BSASigmaA9647for OCM
CHAPSSigmaC3023for ISH
Collagenase ARoche10103578001Defolliculation of oocytes
CysteineSigmaC121800Dejelly embryos
DEPC-H2OFisher ScientificBP5611for ISH
Dig-RNA Labeling MixRoche11277073910for ISH probes
Dumont #5 forcepsWorld Precision Instruments500233for Vitelline envelope removal
Ethyl 3-aminobenzoateSigmaA5040MS222 anesthetic
Ficoll PM 400SigmaF4375for Injection media
FormamideSigmaF9037for ISH
Gentamicin sulfateSigmaG1914for OCM
Glass capillariesWorld Precision Instruments48783.5" long, I,D, 0.530 mm
Glass sample vialsFisher Scientific06-408Bfor ISH
Hair loopHair affixed in pasteur pipette for tissue manipulation
Heparin sodium saltSigmaH4784for ISH
Injector Nanoliter 2010World Precision InstrumentsNanoliter 2010Microprocessor-controlled microinjector
Instant OceanCarolina972433Aquarium Salt for frog recovery
IRBG XGC Xenopus verified full-length cam cDNASource Bioscience989_IRBGcDNA library 
LB Agar plates with 100 µg/ml AmpicillinTeknovaL5004150 mm pre-poured LB-Amp plates for sib selection
LB Luria BrothTeknovaL8650LB for collecting colonies in sib selection from plates and dilution of cultures
Magnetic mRNA Isolation KitNew England BioLabsS1550Sfor isolation of poly(A)-enriched RNA
Maleic AcidSigmaM0375for ISH
Manual Microfil MicromanipulatorWorld Precision InstrumentsM3310RManual micromanipulator
Nutating MixerFisher Scientific22-363-152Rocker for ISH
PermoplastNascoSB33495MClay for injection and dissection dishes
Phosphate Buffered SalineSigmaP5368for ISH
PMSGSigmaG4877to stimulate oocyte development
PolyvinylpyrrolidoneSigmaPVP40for ISH
Programmable PullerWorld Precision InstrumentsPUL-1000Micropipette needle puller
Proteinase KSigmaP6556for ISH
pTnT VectorPromegaL5610cDNA library construction
Riboprobe Combination SystemPromegaP1450in vitro transcription
Superscript Full Length cDNA Library Construction KitLife Technologies18248013kit for cDNA library construction
Sutures, 3-0 silkFisher Scientific19-037-516Suture thread and needle for post-oocyte removal
Torula RNASigmaR3629for ISH
TriethanolamineSigmaT1502for ISH
Tween 20SigmaP9416for ISH
Universal RiboClone cDNA Synthesis SystemPromegaC4360alternative kit for cDNA library construction
Xenopus Full ORF Entry Clones - ORFeome CollaborationSource Bioscience5055_XenORFeomeORFeome Clones
XL2-Blue Ultracompetent CellsAgilent Technologies200150cells for transformation of cDNA library

References

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  1. Yergeau, D., Kelley, C., Zhu, H., Kuliyev, E., Mead, P. Forward Genetic Screens in Xenopus. Using Transposon-Mediated Insertional Mutagenesis. Methods in Molecular Biology. 917, 111-127 (2012).
  2. Grainger, R.

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Tags

Xenopus Oocyte Expression SystemAnimal Cap AssayFunctional CloningmRNA InjectionEmbryonic InductionLens Placode MarkerIn Situ HybridizationOocyte IsolationTissue RecombinationDevelopmental Biology

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