ATAC-seq from nuclei from frozen tissue
Eric RA Pederson
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
All steps should be performed on ice or at 4°C
.
Pre-chill all Dounces and pestles to 4°C
in a fridge or on ice
Pre-chill all tubes.
For each sample you are processing, you will need:
(i) One 2mL
(ii) Three
(iii) one PCR tube per sample
(iv) One
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
i) 6x Homogenization Buffer stable Solution.
A | B |
---|---|
Amount | Reagents |
3 ml | 1 M CaCl2 |
0.6 ml | 3 M Mg(Ac)2 |
6 ml | 1 M Tris pH 7.9 |
89.2 ml | molecular grade water |
6x Homogenization Buffer Stable
ii) 6x Homogenization Buffer Unstable Solution.
A | B |
---|---|
Amount | Reagents |
2.27084 ml | 6x Homogenization Buffer stable |
3.78 ml | 100mM PMSF |
0.28 ul | 14.3 M B-mercaptoethanol |
1/2 tablet | Protease inhibitor (cOmplete Mini) |
6x Homogenization Buffer Unstable Solution
ii) 1x Homogenization Buffer Unstable Solution.
A | B |
---|---|
Amount | Reagents |
2.166645 ml | 6x Homogenization Buffer Unstable Solution |
4.16 ml | 1 M sucrose |
2.6 ul | 500 mM EDTA |
130 ul | 10.00% NP10 |
6.540755 ml | H2O |
1x Homogenization Buffer Unstable Solution
iii) ATAC-RSB:
A | B |
---|---|
Amount | Reagents |
500ul | 1M Tris-Hcl ph 7.5 |
100ul | 5M NaCl |
150ul | 1M MgCl2 |
49.25ml | H2O |
ATAC-RSB
iv) ATAC-RSB + 10% Tween
A | B |
---|---|
Amount | Reagents |
8 ml | ATAC-RSB |
8 ul | 10% Tween |
ATAC-RSB + 10% Tween
v) 2X TD buffer
A | B |
---|---|
Amount | Reagents |
2 ml | 1 M Tris-Hcl pH 7.5 |
1 ml | 1 M MgCl2 |
20 ml | 100% Dimethyl Formamide |
2X TD buffer (before the addition of dimethyl formamide, adjust the pH to 7.6 with 100% acetic acid)
vi) 2X DF buffer
A | B |
---|---|
Amount | Reagents |
100 mM | HEPES (pH 7.2) |
200 mM | NaCl |
0.2 mM | EDTA |
2 mM | DTT |
2.00% | Triton X-100 |
20.00% | Glycerol |
2X DF buffer
Tn5 assembly reaction
A | B | C |
---|---|---|
Primer | Sequence | Amount |
Tn5-A primer | TCGTCGGCAGCGTCAGATGTGTATAAGAGACAG | 16 ul |
Tn5-rev primer | CTGTCTCTTATACACATCT | 16 ul |
Tube A
A | B | C |
---|---|---|
Primer | Sequence | Amount |
Tn5-B primer | GTCTCGTGGGCTCGGAGATGTGTATAAGAGACAG | 16 ul |
Tn5-rev primer | CTGTCTCTTATACACATCT | 16 ul |
Tube B
95°C
to 25°C
cooling -0.1°C/second
~1 hour on PCR machine
Olgio Annealing program
TN5 Assembly
A | B |
---|---|
Amount | Reagent |
25 ul | Tn5 |
15.5 ul | Tube A |
15.5 ul | Tube B |
33 ul | 2X 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
Materials for the cutting of tissue on dry ice.
-
Gloves
-
White warm gloves
-
Dry ice
-
Blades and handle
-
Forceps
-
Ethanol spray
-
Cell culture dish
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.
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
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
.
Dounce with “A” loose pestle until resistance goes away (~10 strokes).
Put the A pestle into the beaker of water
Dounce with “B” tight pestle for 20 strokes.
Put the B pestle into the beaker of water
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.
Let it drip through for 10-15 minutes.
Transfer to a labelled 2mL
Lobind Eppendorf tube, already cold from sitting in ice.
To pellet the nuclei, centrifuge 900rpm,4°C
Transfer the supernatant to a new tube without disturbing the pellet
Repeat the centrifugation
Discard supernatant
Resuspend the nuclei in 200µL
of ATAC-RSB + 10% Tween
Count the amount of cells using the cell counter in the cell lab.
Put 10µL
Trypton blue onto a piece of parafilm and mix with 10µL
of the sample
Take 10µL
of the mix and pipette into a cell counting cell
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.
Calculate the amount of nuclei to use for the next step;
(500000 nuclei)
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
Turn on the thermomixer to 37°C
ATAC-seq
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.
Centrifuge nuclei for 0h 10m 0s
900rcf,4°C
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
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
Add the reaction mix to the pellet and remaining water and resuspend the pellet in the mix
A | B |
---|---|
Amount | Reagents |
25 ul | 2X TD buffer |
16.5 ul | 1X PBS (cold) |
0.5 ul | 1% digitonin |
0.5 ul | 10% Tween -20 |
2.5 ul | TN5 assembly |
Reaction Mix
Put the tube into the thermomixer at 1000rpm
Take the tubes out and immediately proceed to the column clean up
Use the Zymo DNA clean & concentrator to clean the nuclei
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
Transfer mixture to a provided Zymo-spin column in a collection tube
Centrifuge 10000x g
Discard supernatant
Add 200µL
DNA wash buffer to the column
Centrifuge 10000x g
repeat the wash step
Trasnfer the column to a 1.5 low-bind eppendorf tube.
Add 21µL
2 DNA Elution buffer to the column.
Centrifuge 10000x g
Can stop here and start the next day if necessary.
Leave samples in 4°
Set up PCR;
A | B |
---|---|
Amount | Reagent |
2.5 ul | Primer AD1 |
2.5 ul | Primer AD2.# |
25 ul | NEBNext Master Mix |
20 ul | sample |
PCR
PCR program - ATAC-seq pre-amplification
A | B | C |
---|---|---|
Tempurature | Time | Cycle |
72° | 5 minutes | 1 |
98° | 30 seconds | - |
98° | 10 seconds | 5 |
63° | 30 seconds | - |
72° | 1 minute | - |
72 | 5 minutes | 1 |
4 | infinate | - |
ATAC-seq pre-amplification
Remove PCR tubes from the machine and put immediately onto ice.
Proceed immediately to the qPCR amplification to determine additional cycles step
qPCR amplification to determine additional cycles
prepare a mix or master mix
A | B | C |
---|---|---|
Reagent | 1X | 6.5X |
Molecular grade water | 3.76 ul | 24.5 ul |
Primer AD1 | 0.5 ul | 6.5 ul |
Primer AD2.# | 0.5 ul | 0.5 ul * |
25x SYBR green (in DMSO) | 0.24 ul | 1.56 ul |
2x NEBNext Master Mix | 5 ul | 32.5 ul |
qPCR mix
qPCR program
A | B | C |
---|---|---|
Tempurature | Time | Cycle |
98° | 30 seconds | 1 |
98° | 10 seconds | 20 |
63° | 30 seconds | - |
72° | 1 minute | - |
qPCR program
qPCR extra setup options
-
6 machine not 6
-
standard
-
SYBR green
-
no melt curve
-
turn off ROX
-
Fill in sample list
Determine the required amount of cycles that each sample needs in addition
Looking at the final amplification curve, determine the max fluorescence where the graph plateaus
Determine 1/3 of that number.
For example if the max is 1400000 then 1/3 would be 433333
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
Continue the PCR with the additional amount of cycles skipping the beginning parts of the program
of addtional cycles
A | B | C |
---|---|---|
Tempurature | Time | Cycle |
98° | 10 seconds | Based on calculation |
63° | 30 seconds | - |
72° | 1 minute | - |
4° | Infinate | 1 |
Additional cycles
Take the tubes out and immediately proceed to the column clean up
Use the Zymo DNA Clean & Concentrator to clean the nuclei
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
Transfer mixture to a provided Zymo-spin column in a collection tube
Centrifuge 10000x g
Discard supernatant
Add 200µL
DNA wash buffer to the column
Centrifuge 10000x g
Repeat the wash step
Transfer the column to a 1.5 low-bind Eppendorf tube.
Add 21 ul Sterile water buffer to the column.
Centrifuge 10000x g
Quality control
TapeStation (DS1000) and Qubit quantification