ATAC-seq from nuclei from frozen tissue

Eric RA Pederson

Published: 2023-05-14 DOI: 10.17504/protocols.io.bp2l6b4nkgqe/v1

Abstract

Modified ATAC-seq method for frozen tissue, in this case brain tissue.

Before start

The pre-experimentation steps are important

Also it is important that all the primers have been ordered and reconstituted beforehand.

Steps

Pre-experimentation

1.

All steps should be performed on ice or at 4°C.

2.

Pre-chill all Dounces and pestles to 4°C in a fridge or on ice

3.

Pre-chill all tubes.

For each sample you are processing, you will need:

(i) One 2mL per sample

(ii) Three per sample

(iii) one PCR tube per sample

(iv) One for filtration step per sample

4.

Prepare buffers.

i) 6x Homogenization Buffer Stable Solution.

ii) 6x Homogenization Buffer Unstable Solution.

iii) 1x Homogenization Buffer Unstable Solution.

iv) ATAC-RSB

v) ATAC-RSB + 10% Tween

vi) 2X TD buffer

vii) 2X DF buffer

4.1.

i) 6x Homogenization Buffer stable Solution.

AB
AmountReagents
3 ml1 M CaCl2
0.6 ml3 M Mg(Ac)2
6 ml1 M Tris pH 7.9
89.2 mlmolecular grade water

6x Homogenization Buffer Stable

4.2.

ii) 6x Homogenization Buffer Unstable Solution.

AB
AmountReagents
2.27084 ml6x Homogenization Buffer stable
3.78 ml100mM PMSF
0.28 ul14.3 M B-mercaptoethanol
1/2 tabletProtease inhibitor (cOmplete Mini)

6x Homogenization Buffer Unstable Solution

4.3.

ii) 1x Homogenization Buffer Unstable Solution.

AB
AmountReagents
2.166645 ml6x Homogenization Buffer Unstable Solution
4.16 ml1 M sucrose
2.6 ul500 mM EDTA
130 ul10.00% NP10
6.540755 mlH2O

1x Homogenization Buffer Unstable Solution

4.4.

iii) ATAC-RSB:

AB
AmountReagents
500ul1M Tris-Hcl ph 7.5
100ul5M NaCl
150ul1M MgCl2
49.25mlH2O

ATAC-RSB

4.5.

iv) ATAC-RSB + 10% Tween

AB
AmountReagents
8 mlATAC-RSB
8 ul10% Tween

ATAC-RSB + 10% Tween

4.6.

v) 2X TD buffer

AB
AmountReagents
2 ml1 M Tris-Hcl pH 7.5
1 ml1 M MgCl2
20 ml100% Dimethyl Formamide

2X TD buffer (before the addition of dimethyl formamide, adjust the pH to 7.6 with 100% acetic acid)

4.7.

vi) 2X DF buffer

AB
AmountReagents
100 mMHEPES (pH 7.2)
200 mMNaCl
0.2 mMEDTA
2 mMDTT
2.00%Triton X-100
20.00%Glycerol

2X DF buffer

5.

Tn5 assembly reaction

5.1.
ABC
PrimerSequenceAmount
Tn5-A primerTCGTCGGCAGCGTCAGATGTGTATAAGAGACAG16 ul
Tn5-rev primerCTGTCTCTTATACACATCT16 ul

Tube A

ABC
PrimerSequenceAmount
Tn5-B primerGTCTCGTGGGCTCGGAGATGTGTATAAGAGACAG16 ul
Tn5-rev primerCTGTCTCTTATACACATCT16 ul

Tube B

95°C to 25°C

cooling -0.1°C/second

~1 hour on PCR machine

Olgio Annealing program

5.2.

TN5 Assembly

AB
AmountReagent
25 ulTn5
15.5 ulTube A
15.5 ulTube B
33 ul2X DF buffer

Tn5 Assembly Mix

Room temperature 1h 0m 0s

Tn5 from the Protein Science Facility at the Karolinska Institutet in Stockholm (Picelli et al. ,2014)

or

Nuclei extraction and filtration

6.

Materials for the cutting of tissue on dry ice.

6.1.
  • Gloves

  • White warm gloves

  • Dry ice

  • Blades and handle

  • Forceps

  • Ethanol spray

  • Cell culture dish

7.

In the most sterile way possible, cut a small piece of tissue, half a pea size or so, and leave it in the petri dish with a marking on the lid, in the dry ice. Weigh it and cut again if needed.

Make sure to use the ethanol to clean everything and be careful not to cut yourself.

8.

Add 2mL 1X HB buffer into the dounce, which is sitting in the ice.

Add 0.2µL 1 M DTT and and 1µL 100X Halt protease inhibitor

9.

Place 20 mg frozen tissue into a pre-chilled 2 ml Dounce containing 1 ml cold 1x HB and let thaw for 0h 5m 0s.

10.

Dounce with “A” loose pestle until resistance goes away (~10 strokes).

Put the A pestle into the beaker of water

11.

Dounce with “B” tight pestle for 20 strokes.

Put the B pestle into the beaker of water

12.

Pour everything from the dounce into a 30 um MACS smartstrainer which is sitting on top of a labelled 50 ml falcon tube sitting in ice.

13.

Let it drip through for 10-15 minutes.

14.

Transfer to a labelled 2mL Lobind Eppendorf tube, already cold from sitting in ice.

15.

To pellet the nuclei, centrifuge 900rpm,4°C

15.1.

Transfer the supernatant to a new tube without disturbing the pellet

Repeat the centrifugation

16.

Discard supernatant

17.

Resuspend the nuclei in 200µL of ATAC-RSB + 10% Tween

18.

Count the amount of cells using the cell counter in the cell lab.

18.1.

Put 10µL Trypton blue onto a piece of parafilm and mix with 10µL of the sample

18.2.

Take 10µL of the mix and pipette into a cell counting cell

18.3.

Measure on the cell counting machine, making sure to adjust for the smaller size of the nuclei.

The machine will think they are dead cells.

19.

Calculate the amount of nuclei to use for the next step;

(500000 nuclei)

19.1.

ATAC-seq requires 50,000 cells for the experiment. So for example if the number of nuclei is;

4.76 x 107

then the calculation will look like this;

50000 / 47600 = 1.10

20.

Turn on the thermomixer to 37°C

ATAC-seq

21.

Add the calculated amount of cells into a2mL lobind eppendorf tube with 1 ml ATAC-RSB + 10% Tween.

So taking the example above one would take 1.10 ul of nuclei in the 200µL ATAC-RSB + 10% Tween to the new tube.

22.

Centrifuge nuclei for 0h 10m 0s 900rcf,4°C

22.1.

Here one can also save the nuclei for later. Simply spin the tube down with the new tube of diluted nuclei, discard the supernatant, add 300µL of the and put in the -20° freezer.

0h 10m 0s 900rcf,4°C

23.

Discard most of the supernatant. Leave a bit in the bottom to ensure that there is enough for the reaction and that the pellet stays intact

24.

Add the reaction mix to the pellet and remaining water and resuspend the pellet in the mix

AB
AmountReagents
25 ul2X TD buffer
16.5 ul1X PBS (cold)
0.5 ul1% digitonin
0.5 ul10% Tween -20
2.5 ulTN5 assembly

Reaction Mix

25.

Put the tube into the thermomixer at 1000rpm

26.

Take the tubes out and immediately proceed to the column clean up

27.

Use the Zymo DNA clean & concentrator to clean the nuclei

27.1.

Add 2-7 volumes of the DNA binding buffer to each volume of DNA sample

So in this case the volume is approximately 50µL , so add 300µL of DNA binding buffer

27.2.

Transfer mixture to a provided Zymo-spin column in a collection tube

27.3.

Centrifuge 10000x g

Discard supernatant

27.4.

Add 200µL DNA wash buffer to the column

Centrifuge 10000x g

27.5.

repeat the wash step

27.6.

Trasnfer the column to a 1.5 low-bind eppendorf tube.

Add 21µL 2 DNA Elution buffer to the column.

Centrifuge 10000x g

28.

Can stop here and start the next day if necessary.

Leave samples in 4°

29.

Set up PCR;

AB
AmountReagent
2.5 ulPrimer AD1
2.5 ulPrimer AD2.#
25 ulNEBNext Master Mix
20 ulsample

PCR

29.1.

PCR program - ATAC-seq pre-amplification

ABC
TempuratureTimeCycle
72°5 minutes1
98°30 seconds-
98°10 seconds5
63°30 seconds-
72°1 minute-
725 minutes1
4infinate-

ATAC-seq pre-amplification

30.

Remove PCR tubes from the machine and put immediately onto ice.

31.

Proceed immediately to the qPCR amplification to determine additional cycles step

32.

qPCR amplification to determine additional cycles

prepare a mix or master mix

ABC
Reagent1X6.5X
Molecular grade water3.76 ul24.5 ul
Primer AD10.5 ul6.5 ul
Primer AD2.#0.5 ul0.5 ul *
25x SYBR green (in DMSO)0.24 ul1.56 ul
2x NEBNext Master Mix5 ul32.5 ul

qPCR mix

32.1.

qPCR program

ABC
TempuratureTimeCycle
98°30 seconds1
98°10 seconds20
63°30 seconds-
72°1 minute-

qPCR program

32.2.

qPCR extra setup options

  • 6 machine not 6

  • standard

  • SYBR green

  • no melt curve

  • turn off ROX

  • Fill in sample list

33.

Determine the required amount of cycles that each sample needs in addition

33.1.

Looking at the final amplification curve, determine the max fluorescence where the graph plateaus

33.2.

Determine 1/3 of that number.

For example if the max is 1400000 then 1/3 would be 433333

33.3.

Check the graph for how many cycles line up with this number from the curve.

In the case above it would be 6 because of where the line was

34.

Continue the PCR with the additional amount of cycles skipping the beginning parts of the program

34.1.

of addtional cycles

ABC
TempuratureTimeCycle
98°10 secondsBased on calculation
63°30 seconds-
72°1 minute-
Infinate1

Additional cycles

35.

Take the tubes out and immediately proceed to the column clean up

36.

Use the Zymo DNA Clean & Concentrator to clean the nuclei

36.1.

Add 2-7 volumes of the DNA binding buffer to each volume of DNA sample

So in this case the volume is approximately 50 ul, so add 300 ul of DNA binding buffer

36.2.

Transfer mixture to a provided Zymo-spin column in a collection tube

36.3.

Centrifuge 10000x g

Discard supernatant

36.4.

Add 200µL DNA wash buffer to the column

Centrifuge 10000x g

36.5.

Repeat the wash step

36.6.

Transfer the column to a 1.5 low-bind Eppendorf tube.

Add 21 ul Sterile water buffer to the column.

Centrifuge 10000x g

37.

Quality control

TapeStation (DS1000) and Qubit quantification

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