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 JoVE Biology

Double Whole Mount in situ Hybridization of Early Chick Embryos

1, 2

1Center for Environmental and Genetic Medicine, Institute of Biosciences and Technology - Texas A&M Health Science Center, 2Center for Environmental and Genetic Medicine, Texas A&M University (TAMU)

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    Summary

    This video demonstrates 2-color whole mount in situ hybridization, a method by which the spatial and temporal expression pattern of 2 different genes can be visualized in young chick embryos. This method was originally introduced by David Wilkinson, Domingos Henrique, Phil Ingham and David Ish -Horowicz.

    Date Published: 10/27/2008, Issue 20; doi: 10.3791/904

    Cite this Article

    Psychoyos, D., Finnell, R. Double Whole Mount in situ Hybridization of Early Chick Embryos. J. Vis. Exp. (20), e904, doi:10.3791/904 (2008).

    Abstract

    The chick embryo is a valuable tool in the study of early embryonic development. Its transparency, accessibility and ease of manipulation, make it an ideal tool for studying gene expression in brain, neural tube, somite and heart primordia formation. This video demonstrates the different steps in 2-color whole mount in situ hybridization; First, the embryo is dissected from the egg and fixed in paraformaldehyde. Second, the embryo is processed for prehybridization. The embryo is then hybridized with two different probes, one coupled to DIG, and one coupled to FITC. Following overnight hybridization, the embryo is incubated with DIG coupled antibody. Color reaction for DIG substrate is performed, and the region of interest appears blue. The embryo is then incubated with FITC coupled antibody. The embryo is processed for color reaction with FITC, and the region of interest appears red. Finally, the embryo is fixed and processed for phtograph and sectioning A troubleshooting guide is also presented.

    Protocol

    Part 1: Fixing the embryos

    1. Fill dissection dish with ice cold depc-PBS. Keep on ice. Open the egg by tapping the shell with forceps and remove shell pieces.
    2. Remove thick albumin with forceps. Tilt yolk sac with coarse forceps so that embryo faces upwards.
    3. Using scissors, cut a square of yolk sac around the embryo.
    4. Using spoon, remove embryo from yolk and place on ice cold depc-PBS.
    5. Under the microscope, remove membranes and yolk and transfer to fixation dish.
    6. Pin down, remove depc-PBS. Replace with 4% PFA in depc-PBS and fix O/N at 4°C.
    7. Remove fixative. Replace with ice cold depc-PBS. Using a blunt end microcapillary needle or a microdissection knife, perforate the nervous system and the heart cavities, to prevent trapping of probe.
    8. Wash 2x 10 mn depc-PBS with 0.1% Tween-20 (PBT). Dehydrate 10 mn each in 25%, 50%, 75% methanol in PBT. Dehydrate embryos twice in 100% methanol. Store at -20°C in methanol.

    Part 2: Prehybridization

    1. Rehydrate embryos 10 mn each in 75%, 50% and 25% methanol in PBT. Wash 2x 10 mn in PBT.
    2. Meanwhile, prepare ice cold fixative (4% paraformaldehyde in PBT). Replace PBT with proteinase K solution (3 ml/vial; final [5?g/ml] in PBT). Make sure the entire vial is exposed to proteinase K solution by gently rolling the vial; see Troubleshooting for exposure times.
    3. Using RNase free Pasteur pipette remove proteinase K and add fixative (2 ml). Immediately place on ice for exactly 20 mn.
    4. All RT washes are performed on nutator. Wash 2x 10 mn in PBT, and 1x 10mn in PBT containing 50% hybridization buffer.
    5. Wash 1x in hybridization buffer. Incubate at 65°C in 2 ml hybridization buffer for 4-5 hr.

    Part 3: Hybridize embryos with probes

    1. DIG and FITC coupled probe synthesis is described in Appendix. The probe expected to give a strong signal, should be synhesized with FITC-containing nucleotides; the weaker probe should be synthesized with with DIG-containing nucleotides.
    2. Prewarm probes in hybridization buffer (500 ng/ml each) using a 2 ml vial. Promptly replace the hybridization buffer with the probe solution. Do not let the embryos dry. Incubate for 16 hr at 65°C.
    3. Replace probe with hybridization buffer, 2 washes, 30 mn each at 65°C. Wash 15 mn in hybridization buffer/MABT (1/1 v/v/) at 65°C.

    Part 4: DIG antibody incubation and color reaction

    1. Wash 2x20 mn in MABT. Wash 1 hr in 2% BBR/MABT. Wash 5 hr in 2% BBR/20%HISS/MABT (blocking buffer). Incubate in 1:2000 DIG antibody diluted in blocking buffer, O/N at 4°C on nutator.
    2. Wash 3x 10 mn each in MABT, and 3x 1 hr each in MABT.
    3. Wash 2x 20 mn in NTMT. Add 200ul NBT/BCIP substrate to 10 ml NTMT. Immediately remove NTMT from vial and replace with 1-2 ml NBT/BCIP buffer. Place in dark. Monitor color reaction after 20 mn, and at 20 mn intervals thereafter.
    4. Following color reaction (should appear blue), wash in PBS for 10 mn, pin down on fixation dish filled with PBS, and replace solution with 4% PFA in PBS. Fix O/N at 4°C.
    5. Transfer to new scintillation vial. Wash in PBST (PBS with 1% Tween-20) 2x10 mn. Wash in MABT 2x 10 mn.
    6. Incubate in MABT 30 mn at 63°C.

    Part 5: FITC antibody incubation and color reaction

    1. Wash 2x 10 mn in MABT, 1 hr in 2%BBR/MABT, 5 hr in blocking buffer
    2. Incubate in alkaline phosphatase-coupled anti-FITC-antibody (1:500) O/N at 4°C.
    3. Wash 3x 10 mn each in MABT, and 3x 1 hr each in MABT.
    4. Wash in 2x 20 mn in TBS pH 8.45 with 0.1% Tween-20 (TBST).
    5. Prepare Vector Red working solution (5 ml) in TBST using reagents 1,2 and 3 provided in kit. Immediately remove TBST from vial and replace with Vector Red buffer. Place in dark. Monitor color reaction after 40 mn, and at 30 mn intervals thereafter.
    6. Following color reaction (should appear red), transfer embryos to PBS.

    Part 6: Fixation and processing

    1. Transfer to fixation dish containing PBS, and fix in 4% PFA for 20 mn at RT or O/N at 4°C.
    2. Wash in PBS, 2x 10 mn. To process for photography, transfer to 20% glycerol in PBS (this will make the embryos translucent). To create a chamber, cut 2 strips of PVC tape, superimpose them on slide. Cut a square in the center using a blade. Remove the square using forceps.
    3. To process for wax sectioning, transfer back to PBS, wash 2x 10 mn, dehydrate in graded series of methanol (25%, 50%, 75% and 100% in PBS, 10 mn each).
    4. Replace with propanol, 3mn. Replace with 1,2,3,4-tetrahydronaphthalene, 20 mn followed by Histoclear (2x 1 hr). Replace with histoclear/wax 1/1 (v/v) 60°C for 1 hr. Replace with wax an process for histology.

    Part 7: Solutions

    Hybridization buffer, store at -20°C in Falcon, 50 ml: 25 ml formamide; 3.25 ml (20xSSC); 0.5 ml (0.5M EDTA); 1 ml (10% Tween-20); 2.5 ml (1% SDS); 125 ul (20mg/ml tRNA); 100ul (50 mg/ml heparin).MABT, prepare 100mM maleic acid; pH to 7.5 with NaOH pellets. Add 150mM NaCl and 0.1% Tween-20.

    NTMT (made just prior to use), 50 ml: 1ml (5M NaCl); 2.5 ml (2M Tris-HCl pH9.5); 1.25 ml (2M MgCl2); 5 ml (10% Tween-20).

    TBST: 0.1M Tris-HCl, 0.15M NaCl, pH 8.45, 0.1% Tween-20.

    Part 8: Troubleshooting

    Problem Cause Remedy
    Embryo is curled up Insufficient dehydration/rehydration Maintain 10 mn intervals during successive dehydration/rehydration steps
    There is no probe signal Probe is degraded RNase contamination in vial Run probe on 1% Agarose gel Make sure that the entire vial is exposed to Proteinase K solution in step 2
    Probe is labels cavities of heart an neural tube Probe is trapped In step 2, make sure that all cavities are perforated using microdissection knife or microcapillary
    Embryo disintegrated following hybridization (step 3) Proteinase K step left too long Hybridization temperature is too high Proteinase K should not be left longer than 1mn (stages 3+ and 4), 2 mn (stage 5 to 7), 3 mn (stage 8-10), 4 mn (stage 11-13) Do not hybridize at To higher than 65 o C

    Part 9: Representative Results

    Representative embryos are  shown below: (A) Embryo (stage HH7) is labelled with a DIG-Sox probe (blue) and a FITC-delta-1  probe (red). (B) Embryo (stage HH8) is labelled with a DIG-Pax6 probe (blue) and a FITC-Shh probe (red). Nf, neural fold, anp, anterior neural plate, psm, presomitic mesoderm, n, notochord, nt, neural tube). Probe gifts from the laboratories of Drs. C. Tabin, M.  Goulding ,  D. Henrique, and J. Briscoe.

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    Discussion

    The 2-color whole mount in situ hybridization method is used to determine both spatial and temporal patterns of gene expression, using one or two genes of interest. Applications include assessment of gene expression patterns of novel genes (e.g. 1,2, as well as changes in gene expression following insult (embryonic manipulations 3, beads 4, and electroporation of RNA or DNA constructs 5).

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    Disclosures

    The authors have nothing to disclose.

    Acknowledgements

    This work was supported by the Margaret M. Alkek Foundation to RHF.

    Materials

    Name Type Company Catalog Number Comments
    Eggs Animal Charles River Laboratories Premium Fertile
    Stereomicroscope Microscope Leica Microsystems MZ9.5
    Marsh Automatic Incubator Tool Lyon RX
    Hybridization Incubator Tool Hybaid Micro-4
    Adams Nutator orbital mixer Tool Fisher Scientific 14-062
    Curved Forceps (1) Tool Electron Microscopy Sciences 72991-4C
    Fine scissors Tool Fine Science Tools 14161-10
    Spoon Tool Fine Science Tools 10370-18
    Pasteur Capillary Pipette Electron Microscopy Sciences 70950-12
    Microcapillary tube Sigma-Aldrich P1049-1PAK Pull using vertical micropipette puller; blunt end with fine forceps
    Microdissecting knife Fine Science Tools 10056-12 Use to puncture cavities prior to in situ hybridization
    Minuten pins 0.2mm diam Fine Science Tools 26002-20 Keep pins together using a magnetic stirrer;
    Sylgard 184 Silicon Elastomer Curing Agent and Base Reagent Dow Corning 0001986475 Mix 1 part Curing Agent, 9 parts Base; set O/N at 37C
    Diethylpyrocarbonate (depc) Reagent Acros Organics 10025025 Add 1ml depc to 1l PBS; shake; autoclave
    16% PFA Reagent Electron Microscopy Sciences 15710
    Tween-20 Reagent Sigma-Aldrich P1379-100ML
    Proteinase K Sigma-Aldrich P2308-5MG Stock at 10 mg/ml in depc-H2O in 10ul aliquots. Store at -20C.
    Formamide, deionized Reagent Ambion 9342
    Yeast tRNA-25 mg Reagent Invitrogen 15401-011 Stock at 20 mg/ml in depc-H2O in 125ul aliquots. Store at -20C
    Heparin Sodium salt Reagent Sigma-Aldrich H4784-250MG Stock at 50 mg/ml in depc-H2O in 100ul aliquots. Store at -20C.
    SSC x20 pH5.5 Reagent Fisher Scientific PR-V4261
    EDTA (0.5M) PR-V4231 Fisher Scientific
    SDS Reagent Fisher Scientific BP166-100
    Maleic acid Reagent Fluka 63189
    B–hringer Blocking Reagent Reagent Roche Group 11096176001 Use at 2% in MABT. To make, heat with MABT for 20 mn at 60C. Can make a stock and store in 1-5 ml aliquots at 20C.
    Heat inactivated sheep serum Reagent Jackson ImmunoResearch 013-000-121 Dissolve in 10 ml H2O; heat 550C, 30 mn. Aliquot at 1ml, -20C.
    Anti-Digoxigenin-AP, Fab fragments Reagent Roche Group 11093274910
    NBT/BCIP stock solution Reagent Roche Group 11681451001
    Anti-Fluorescein-AP, Fab fragments Reagent Roche Group 11426338910
    2M Tris BP1759-500 Fisher Scientific
    Vector Red Alkaline Phosphatase Substrate Kit Reagent Vector Laboratories SK-5100
    1,2,3,4-tetrahydronaphthalene Reagent Sigma-Aldrich 429325-100ML Under hood

    References

    1. Streit, A., Berliner, A.J., Papanayotou, C., Sirulnik, A. & Stern, C.D. Initiation of neural induction by FGF signaling before gastrulation. Nature 406,74-78 (2000).

    2. Rodríguez Esteban, C., Capdevila, J., Economides, A.N., Pascual, J., Ortiz, A. & Izpisúa Belmonte, J.C. The novel Cer-like protein Caronte mediates the establishment of embryonic left-right asymmetry. Nature 401, 243-251 (1999).

    3. Psychoyos, D. & Stern, C.D. Restoration of the organizer after radical ablation of Hensen's node and the anterior primitive streak in the chick embryo. Development 122, 3263-3273 (1996).

    4. Kawakami, M. & Nakanishi, N. The role of an endogenous PKA inhibitor, PKIalpha, in organizing left-right axis formation. Development 128, 2509-2515 (2001).

    5. Basch, M.L., Bronner-Fraser, M. & Garcia-Castro, M.I. Specification of the neural crest occurs during gastrulation and requires Pax7. Nature 441, 218-222 (2006).

    Comments

    1 Comment

    comment from author (DP): Pax6 expressed in neural folds and developing neural tube (Results section)
    Reply

    Posted by: AnonymousOctober 28, 2008, 10:34 AM

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