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    PHYTOMap in Arabidopsis root tips

    Joseph Ecker, Tatsuya Nobori

    Published: 2023-05-24 DOI: 10.17504/protocols.io.rm7vzbp4xvx1/v1
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    Abstract

    Retrieving the complex responses of individual cells in the native three-dimensional tissue context is crucial for a complete understanding of tissue functions. Here, we present PHYTOMap (Plant HYbridization-based Targeted Observation of gene expression Map), a multiplexed fluorescence in situ hybridization method that enables single-cell and spatial analysis of gene expression in whole-mount plant tissue in a transgene-free manner and at low cost. We applied PHYTOMap to simultaneously analyze 28 cell type marker genes in Arabidopsis roots and successfully identified major cell types, demonstrating that our method can substantially accelerate the spatial mapping of marker genes defined in single-cell RNA-seq datasets in complex plant tissue.

    PHYTOMap principles. a, Target mRNA molecules are hybridized by DNA probes (SNAIL probes) that harbor mRNA species-specific barcode sequences (pink bars). The barcode-containing DNA probes are circularized by ligation and amplified in situ by rolling circle amplification (RCA). b, Amplified DNA barcodes are detected by sequence-by-hybridization. Different fluorescent probes target four DNA barcodes for each imaging round. After the imaging, fluorescent probes are stripped away, and another set of four genes is targeted.
    PHYTOMap principles. a, Target mRNA molecules are hybridized by DNA probes (SNAIL probes) that harbor mRNA species-specific barcode sequences (pink bars). The barcode-containing DNA probes are circularized by ligation and amplified in situ by rolling circle amplification (RCA). b, Amplified DNA barcodes are detected by sequence-by-hybridization. Different fluorescent probes target four DNA barcodes for each imaging round. After the imaging, fluorescent probes are stripped away, and another set of four genes is targeted.

    [Reagents]

    DPBST

    0.1% (vol/vol) Tween-20 in 1x DPBS

    DPBSTR

    DPBST + 1:100 SUPERaseIN

    Cell wall digestion enzyme solution (CWDES; 10x stock)

    250 mg macerozyme, 250 mg cellulase, 500 mg pectinase in 50 mL Nuclease-free water. Filter sterilize (0.22 μm filter) and store aliquots of 1 mL at -20°C.

    Proteinase K buffer

    AB
    ReagentAmount
    1M Tris-HCl (pH 8.0)5 mL
    0.5 M EDTA (pH 8.0)5 mL
    Nuclease Free Waterup to 50 mL

    FAA

    AB
    ReagentAmount
    32% formaldehyde450 µL
    Acetic acid50 µL
    Ethanol500 µL

    Steps

    Sampling

    1.

    Cut Arabidopsis root tips (approximately 1 cm) with razor blade and place them on a Poly-D-Lysine coated dish. The tissue should adhere to the dish well.

    Tissue Fixation

    2.

    Incubate the tissue in 100µL of FAA (see MATERIALS) at Room temperature for 1h 0m 0s.

    Note
    If most of the root tips detach from the dish, it is necessary to optimize the mounting process for the samples.

    3.

    Wash the tissue successively for 0h 10m 0s at Room temperature with 100µL 70% EtOH, 90% EtOH, and twice with 100% EtOH.

    4.

    Wash the tissue twice with 100µL 100% MeOH for 0h 10m 0s and leave the tissue in MeOH after the second wash at -20°C 0h 30m 0s.

    Tissue Permeabilization

    5.

    Rehydrate the tissue by 0h 5m 0s successive washes with 100µL 75%, 50%, 25% MeOH in DPBST.

    6.

    Incubate the tissues in 100µL 1x CWDES (see MATERIALS) On ice for 0h 5m 0s.

    AB
    AB
    ReagentAmount
    10x CWDES10 µL
    SUPERase IN1 µL
    DPBST89 µL

    1x CWDES

    7.

    Remove the CWDES and add 100µL fresh & cold 1x CWDES. Then, incubate the tissue at Room temperature for 0h 30m 0s.

    8.

    Wash the tissue twice with 100µL DPBSTR (see MATERIALS).

    9.

    Fix the tissue by incubating in 100µL 10% (v/v) formaldehyde in DPBST at Room temperature for 0h 30m 0s.

    10.

    Wash the tissue twice with 100µL DPBSTR at Room temperature (0h 1m 0s each).

    11.

    Incubate the tissue in 100µL digestion solution at 37°C for 0h 30m 0s.

    AB
    ReagentAmount
    Proteinase K buffer (see MATERIALS)99 µL
    Proteinase K1 µL

    Digestion solution

    12.

    Wash the tissue twice with 100µL DPBSTR at Room temperature (0h 1m 0s each).

    13.

    Fix the tissue by incubating in 100µL 10% (v/v) formaldehyde in DPBST at Room temperature for 0h 30m 0s.

    14.

    Wash the tissue twice with 100µL DPBSTR at Room temperature (0h 5m 0s each).

    Gene Specific Probe Hybridization

    15.

    Mix gene specific probes at the concentration of 5 nM per oligo.

    16.

    Heat the probe mixture at 90°C for 0h 3m 0s and let it cool down at Room temperature.

    17.

    Incubate the tissue in the hybridization mixture at 40°C for 3h 0m 0s or 3h 0m 0s

    AB
    ReagentAmount
    20xSSC10 µL
    Formamide30 µL
    10% Triton-X10 µL
    200 mM RVC10 µL
    SUPERase IN1 µL
    Probe mix (500 nM per oligo)2 µL
    Nuclease Free Water37 µL

    Hybridization mixture

    Note
    The design of probes is described in our paper. The design of probes is described in our paper. .

    18.

    Wash the tissue twice with 100µL DPBSTR at 37°C for 0h 30m 0s.

    19.

    Wash the tissue twice with 100µL 4xSSC in DPBSTR at 37°C for 0h 30m 0s.

    AB
    ReagentAmount
    20xSSC20 µL
    DPBST79 µL
    SUPERase IN1 µL

    4xSSC in DPBSTR

    20.

    Rinse the tissue with 100µL DPBSTR at Room temperature.

    Ligation

    21.

    Incubate the tissue in 100µL ligation mixture WITHOUT ligase On ice for 0h 5m 0s.

    AB
    ReagentAmount
    10x ligation buffer10 µL
    BSA (2mg/ml)0.5 µL
    SUPERase IN1 µL
    Nuclease Free Water88.5 µL

    Ligation mixture without ligase

    22.

    Incubate the tissue in 100µL ligation mixture WITH ligase at Room temperature .

    AB
    ReagentAmount
    10x ligation buffer10 µL
    BSA (20 mg/ml)0.5 µL
    SUPERase IN1 µL
    T4 DNA ligase2 µL
    Nuclease Free Water86.5 µL

    Ligation mixture

    Rolling Circle Amplification (RCA)

    23.

    Wash the tissue with 100µL DPBSTR for 0h 5m 0s.

    24.

    Incubate the tissue in 100µL RCA mixture WITHOUT equiPhi29 DNA polymerase On ice for 0h 5m 0s.

    AB
    ReagentAmount
    10x equiPhi29 DNA polymerase buffer10 µL
    10 mM dNTP2.5 µL
    4 mM aminoallyl-dUTP0.5 µL
    BSA (20 mg/ml)0.5 µL
    DTT (100 mM)1 µL
    SUPERase IN1 µL
    Nuclease Free Water84.5 µL

    RCA mixture without equiPhi29 DNA polymerase

    25.

    Incubate the tissue in 100µL RCA mixture WITH equiPhi29 DNA polymerase at 37°C 0h 5m 0s.

    AB
    ReagentAmount
    10x equiPhi29 DNA polymerase buffer10 µL
    10 mM dNTP2.5 µL
    4 mM aminoallyl-dUTP0.5 µL
    BSA (20 mg/ml)0.5 µL
    DTT (100 mM)1 µL
    SUPERase IN1 µL
    equiPhi29 DNA polymerase5 µL
    Nuclease Free Water79.5 µL

    RCA mixture with equiPhi29 DNA polymerase

    26.

    Wash the tissue twice with 100µL DPBSTR for 0h 10m 0s.

    Post-Amplification Fixation

    27.

    Incubate the tissue in 100µL BS(PEG9) solution at Room temperature for 1h 0m 0s.

    AB
    ReagentAmount
    DPBST98 µL
    BS(PEG9) stock2 µL

    BS(PEG9) solution

    Note
    BS(PEG9) stock is made by adding 465 µL DMSO into a vial of 100 mg BS(PEG9) and is stored desiccated at -20ºC.

    28.

    Aspire BS(PEG9) solution and incubate the tissue in 100µL 1 M Tris-HCl pH 8.0 at Room temperature for 0h 30m 0s.

    29.

    Rinse the tissue in 100µL DPBST.

    Note
    If multiple rounds of imaging are not necessary, gel embedding may be skipped. However, it is important to note that without gel embedding, there is a higher risk of tissue detachment or movement between imaging rounds. Therefore, it is recommended to carefully handle the tissue.

    Gel Embedding

    30.

    Incubate the tissue in 100µL monomer solution On ice for 0h 30m 0s.

    AB
    ReagentAmount
    20% acrylamide20 µL
    2% bis-acrylamide10 µL
    2xSSC70 µL

    Monomer solution

    31.

    Aspire the monomer solution and add 50µL gelling solution. Place a Gel Slick-coated glass coverslip on top of the tissue, and carefully aspirate any excess gelling solution. Incubate the tissue at Room temperature for 1h 0m 0s––2h 0m 0s until the gel solidifies.

    AB
    ReagentAmount
    Monomer solution48.9 µL
    10% APS stock1 µL
    TEMED0.1 µL

    Gelling solution

    Note
    Coating a coverslip with Gel Slick:Add Gel Slick Solution onto the coverslip, then wipe gently with a Kimwipe to spread the Gel Slick Solution.

    32.

    Carefully remove the coverslip with forceps, and wash the tissue with 100µL DPBST for 0h 5m 0s.

    33.

    Incubate the tissue in ClearSee until imaging.

    Target Detection with Sequence-By-Hybridization

    34.

    Wash the tissue twice with100µL 2xSSC for 0h 1m 0s.

    35.

    Incubate the tissue in 100µL Bridge probe mixture at Room temperature for 1h 0m 0s.

    AB
    ReagentAmount
    2x hybridization buffer50 µL
    Bridge probes (10uM stock)1 µL each (typically 4 probes)
    Nuclease free waterup to 100 µL

    Bridge probe mixture

    36.

    Wash the tissue twice with 100µL 2xSSC for 0h 1m 0s.

    37.

    Incubate the tissue in 100µL Detection probe mixture at Room temperature for 1h 0m 0s.

    AB
    ReagentAmount
    2x hybridization buffer50 µL
    Detection probes (10uM stock)1 µL each (4 probes)
    Calcofluor White1 µL
    Nuclease free waterup to 100 µL

    Detection probe mixture

    38.

    Wash the tissue twice with 100µL 2xSSC for 0h 1m 0s.

    39.

    Wash the tissue with 100µL ClearSee, and keep it in ClearSee for imaging.

    40.

    Imaging with a confocal microscope.

    41.

    After the imaging, strip the bridge/detection probes by incubating the tissue in100µL stripping solution (65% formamide in 2xSSC) at 30°C for 0h 30m 0s.

    AB
    ReagentAmount
    Formamide65 µL
    20xSSC10 µL
    Nuclease free waterup to 100 µL

    Stripping solution

    42.

    Go to Step 35 for the next round of imaging.

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