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In This Article

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

Summary

The present protocol describes designing, preparing, and microinjecting a translational-blocking morpholino against a representative cardiac gene; Heart And Neural Crest Derivatives Expressed2 (hand2) into the yolk of newly fertilized zebrafish embryos to knock down gene function. It also shows a transient rescue of these "morphants" by co-injection of mRNA encoding this gene product.

Abstract

The morpholino oligomer-based knockdown system has been used to identify the function of various gene products through loss or reduced expression. Morpholinos (MOs) have the advantage in biological stability over DNA oligos because they are not susceptible to enzymatic degradation. For optimal effectiveness, MOs are injected into 1-4 cell stage embryos. The temporal efficacy of knockdown is variable, but MOs are believed to lose their effects due to dilution eventually. Morpholino dilution and injection amount should be closely controlled to minimize the occurrence of off-target effects while maintaining on-target efficacy. Additional complementary tools, such as CRISPR/Cas9 should be performed against the target gene of interest to generate mutant lines and to confirm the morphant phenotype with these lines. This article will demonstrate how to design, prepare, and microinject a translation-blocking morpholino against hand2 into the yolk of 1-4 cell stage zebrafish embryos to knockdown hand2 function and rescue these "morphants" by co-injection of mRNA encoding the corresponding cDNA. Subsequently, the efficacy of the morpholino microinjections is assessed by first verifying the presence of morpholino in the yolk (co-injected with phenol red) and then by phenotypic analysis. Moreover, cardiac functional analysis to test for knockdown efficacy will be discussed. Finally, assessing the effect of morpholino-induced blockage of gene translation via western blotting will be explained.

Introduction

The utilization of zebrafish as a model for the study of cardiovascular development and disease offers a variety of advantages, including high conservation of gene function, optical transparency, rapid cardiovascular development, and cheaper cost when compared to traditional in vivo models1. Morpholino oligonucleotides (MOs) are the most commonly used antisense gene knockdown tools for the zebrafish model. MOs are frequently used to determine a phenotype or to probe gene function. Dr. James Summerton initially developed the morpholino delivery system for the in vivo inhibition of mRNA translation as an attempt to develop thera....

Protocol

All experiments were carried out in accordance with the accepted standards of humane animal care under the regulation of the IACUC at QU; animals were held in the zebrafish facility under Qatar University Biomedical Research Center (QU-BRC). All animals used in these experimental studies were under 3 days post-fertilization (dpf).

NOTE: For each experimental group, it is advisable to use at least 30 embryos for statistical rigor. The experimental groups are as follows:

Representative Results

The graph in Figure 6 illustrates the average percent of embryos surviving at 24, 48, and 72 hpf for both HAND2- specific MO and control scrambled MO-injected embryos. The 1 mM (8 ng/µL) and 0.8 mM (6.4 ng/µL) MO-injected embryos showed a significant reduction in survival percentage compared to control scrambled MO-injected embryos. This was observed across each measured time point where lethality or malformation was observed. The results indicated that a high concentration of HAND.......

Discussion

Morpholino (MO) technology has been extensively used in zebrafish, xenopus, sea urchins, and more recently in cell culture model systems. With most methods, along with the benefits, there are also pitfalls that the experimenter should be aware of. One of the major pitfalls with MO technology includes the concern that phenotypic effects observed by the MO-mediated gene knockdown approach are not due to the loss of function associated with the primary gene product but that some other genes along with the primary gene or in.......

Acknowledgements

The publication of this article was covered with a generous support from BARZAN HOLDINGS. RR is partly supported by R61HL154254 and funds from Department of Pediatrics and Children’s Hospital. 

....

Materials

NameCompanyCatalog NumberComments
Acrylamide 40%SigmaSigma, cat. no. C977M88
AgaroseSigma-AldrichSigma-Aldrich cat. no A9539-250G
All Prep DNA/RNA Mini KitQiagenQiagen cat. no. 80204.
alpha TubulinAbcamAbcam- ab4074Rabbit polyclonal to alpha Tubulin lot GR3 180877-1 (50 kDa)
Ammonium persulfate molecular gradeSigmaSigma, cat. no C991U65
BV10 capillary bevellerSutter Instruments ProductSutter Instruments Product Catalog # BV10
Chemiluminescence Imaging Gene GnomeSYNGENESYNGENE
Cleaver Scientific BlottingCVS10D_OmniPAGEMiniCVS10D_OmniPAGEMini
CoomassieThermo FisherThermo Fisher cat. no C861C44
Electrochemiluminescence (ECL) kitAbcam BiochemicalsAbcam Biochemicals cat. no ab65623
GlycineSigmaSigma, cat. no C988U91
Goat anti RabbitAbcamAbcam-  ab6721Goat Anti-Rabbit IgG H&L (HRP) 2nd antibodies lot GR3179871-1
HAND2Gene toolsCustom made for HAND2 (NM_021973)5'-CCTCCAACTAAACTCATGGCGAC
AG-3'
Hand2AbcamAbcam- ab10131Rabbit polyclonal Anti-HAND2 antibody lot GR143200-9 (24- 26 kDa)
HAND2 (NM_021973) Human Tagged ORF CloneOriGene Technologies, IncRC224436L3Vector: pLenti-C-Myc-DDK-P2A-Puro (PS100092)
IBI DNA/RNA/Protein Extraction KitIBI ScientificIBI Scientific cat. no -r IB47702
Imaging SystemiBrightiBright CL1000 Imaging System
IsopropanolSigma-AldrichSigma-Aldrich cat. no 278475-2L
Laemmli sample loading buffer (4x)Sigma-AldrichSigma-Aldrich cat. no 70607
MercaptoethanolSigmaSigma, cat. no M6250-1L
Microplate Spectrophotometer with the Gen5 Data Analysis software interfaceEpochEpoch
MicroscopeZiess SteREO Lumar V12 Flourescence MicroscopeZiess SteREO Lumar V12 Flourescence Microscope
Mineral oilFisher ScientificFisher Scientific cat. no 0121-1
mMESSAGE mMACHINE T7/T3/SP6 Transcription KitThermo FisherThermo Fisher cat. no.AM1340for mRNA generation
Nuclease-free waterNew England BiolabsNew England Biolabs cat. no B1500L
PC-100 Micropipette PullerNARISHIGE GROUP ProductNARISHIGE GROUP Product Catalog # PC-100
Phenol redSigmaSigma, cat. no. P-0290
Picolitre InjectorHarvard ApparatusHarvard Apparatus cataloge # PLI-90A
Pierce Bicinchoninic acid assay (BCA) Protein Assay kitThermo FisherThermo Fisher cat. no 23227
PMSF, Protease inhibitor as protease inhibitorsThermo FisherThermo Fisher cat. no 36978
Ponceau SSigma-AldrichSigma-Aldrich cat. no 10165921001
Protease Inhibitor CocktailThermo FisherThermo Fisher cat. no 88668
Protein ladderSMOBiOSMOBiO cat. no PM2500
Radioimmunoprecipitation Assay (RIPA)Thermo FisherThermo Fisher cat. no 89900
Ringer’s solutionThermofisherCatalog No.S25513
SDSSigmaSigma, cat. no 436143
Standard ControlGene toolsSKU: PCO-StandardControl-1005'-CCTCTTACCTCAGTTACAATTTAT
A-3'- that targets a human beta-globin intron mutation
Stripping bufferSigma-AldrichSigma-Aldrich cat. 21059
TemedIBI scientificIBI scientific cat. no C000A52
Tris BaseThermo FisherThermo Fisher cat. no BP-152-500
Tweensigma life sciencesigma life science cat. no P2287
Zebra Box Revolution-Danio Track system chamber with the EthoVision XT 11.5 softwareNoldus Information Technology, NLNoldus Information Technology, NL
Zeiss Axiocam ERc 5sZeissStemi 508 Zeiss
Zeiss Stemi 2000-CZeissStemi 2000-C

References

  1. Bakkers, J. Zebrafish as a model to study cardiac development and human cardiac disease. Cardiovascular Research. 91 (2), 279-288 (2011).
  2. Bill, B. R., Petzold, A. M., Clark, K. J., Schimmenti, L. A., Ekker, S. C. A primer for morpholino....

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