Whole-Mount In Situ Hybridization of RNA Probes to Plant Tissues (original) (raw)

Protocol

1. Jan Traas

This protocol was adapted from “How to Study Gene Expression,” Chapter 7, in Arabidopsis (eds. Weigel and Glazebrook). Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY, USA, 2002.

INTRODUCTION

The labeling of entire plantlets (whole-mount labeling) is very easy, but it can cause substantial artifacts. Because whole plants are labeled, certain tissues are not readily accessible to the probes, whereas others can often stain nonspecifically. In the hands of the author, for instance, the elongation zone of the root is labeled even in negative controls, whereas mature parts of the roots and hypocotyl tend to be more resistant to probe penetration. Whole-mount labeling should therefore only be used to monitor gene expression in a limited number of organs and tissues--in particular, root meristems, embryos, and very young primordia--and the results should be interpreted with care. A protocol for whole-mount labeling is described here. Positive (e.g., constitutive probe) and negative controls should be included systematically.

MATERIALS

Reagents

Acetone powder prepared from plant tissue (optional; see Step 18)

Antibody (anti-DIG, alkaline phosphatase-conjugated)

Blocking reagent (e.g. in DIG Nucleic Acid Detection kit [Roche Applied Science]) (optional; see Step 18)

5-bromo-4-chloro-3-indolyl-phosphate 4-toluidine (BCIP) (50 mg/mL)

Detection buffer

Dimethyl sulfoxide (DMSO) (optional; see Step 1)

Ethanol (series of 30%, 60%, 70%, 85%, 95%, 100%) (Steps 2 and 23)

Formaldehyde (4%, v/v in PBS)

Prepare fresh from paraformaldehyde.

Histoclear

Hybridization buffer (whole-mount) (HBWM)

Methanol

4-nitro blue tetrazolium chloride (NBT) (100 mg/mL)

PBT

PBTF (PBT + 4% formaldehyde)

PBTK (PBT + proteinase K, 40 μg/mL; may be reduced if necessary)

Permount

Phosphate-buffered saline (PBS) (1X)

Plant tissue of interest

Use only small samples such as young seedlings, young roots, meristems.

Probe (DIG-labeled) (from Preparation and Hydrolysis of Digoxygenin-Labeled Probes for In Situ Hybridization of Plant Tissues)

TE buffer

Xylene

Equipment

Heating block preset to 80ºC

Ice

Microscope (dissecting)

Pipettes (Pasteur)

Tubes (microcentrifuge)

Vials (scintillation)

Water bath preset to 55ºC

METHOD

Fixation and Dehydration

• 1. Fix plant tissue in a scintillation vial using 4% (v/v) formaldehyde in PBS as follows:
  • i. Fix the tissue for 30 min at room temperature; if necessary, place under vacuum for 15 min.
  • ii. Leave the tissue in fixative overnight at 4ºC.
    Adding 10% DMSO to the fixative can sometimes improve the results.
• 2. Dehydrate the samples through an ethanol series: 30%, 60%, 70%, 85%, 95%, 100%, 100%, for 30 min each.
• 3. Leave the samples in 100% ethanol for 2-4 d at -20ºC.
  This helps to reduce background staining, but it does make the samples brittle.
• 4. Transfer a small number of samples of tissue to a microcentrifuge tube (e.g., up to four 5-d-old plantlets per tube).

Pretreatment

• 5. Wash the samples twice with 100% ethanol.
  If necessary, use a drawn-out Pasteur pipette to remove the ethanol. Be careful; the samples are fragile.
• 6. Wash the samples in xylene for 30 min.
• 7. Wash the samples four times in 100% ethanol, followed by twice in methanol.
• 8. Prepare 50% (v/v) methanol/50% (v/v) PBTF and transfer the tissue to this solution. Incubate for 5 min.
• 9. Post-fix the tissue in PBTF for 25 min and wash five times in PBT for 10 min per wash.
• 10. Incubate the samples in PBTK for 10 min and wash four times in PBT for 5 min per wash.
• 11. Post-fix the tissue in PBTF for 25 min and wash four times in PBT for 5 min per wash. Leave the tissue in PBT for 60 min. Add an equal volume of HBWM to the last wash.
• 12. Rinse the tissue twice in HBWM.

Hybridization and Wash

• 13. Prehybridize in HBWM for 3 h at 55ºC in a water bath.

• 14. Denature the DIG-labeled probe for 2-5 min at 80ºC, and place on ice.

• 15. Replace the buffer used for prehybridization with fresh prewarmed HBWM. Add the denatured DIG-labeled probe in 1-5 μL.

• 16. Hybridize for 18 h (i.e., overnight) at 55ºC.

• 17. Wash the samples as follows:

  • i. Wash six times in HBWM for 30 min per wash.
  • ii. Prepare 75% (v/v) HBWM/25% (v/v) PBT. Wash for 20 min in this solution.
  • iii. Prepare 50% (v/v) HBWM/50% (v/v) PBT. Wash for 20 min in this solution.
  • iv. Prepare 25% (v/v) HBWM/75% (v/v) PBT. Wash for 20 min in this solution.
  • v. Wash four times in PBT for 5 min per wash.

• 18. Replace the PBT with 500 μL of PBT + antibody (diluted 1:2000).
  If necessary, blocking reagent can be added according to the manufacturer’s instruction. The antibody may also be preadsorbed with an acetone powder made from plant tissue. Incubate overnight in the cold.

• 19. Wash the tissue in PBT for at least 3 h, changing the PBT several times.

• 20. Equilibrate the tissue for 5 min in detection buffer.

• 21. Add 150 μL of NBT (100 mg/mL) and 150 μL of BCIP (50 mg/mL) per 100 mL of detection buffer. Incubate the tissue in the NBT/BCIP solution in the dark. Check under a dissecting microscope after 12 h. Incubate for a total of up to 36 h (or longer).

• 22. Stop the enzyme reaction in TE buffer.

• 23. Dehydrate the tissue through an ethanol series (90 sec each), followed by Histoclear, twice for 90 sec.

• 24. Mount with Permount.

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