Exercise 10.3 - Extraction of Chromatin



Procedure 3

  1. Homogenize approximately 30 gms of bovine or porcine cerebellar tissue in a teflon-glass homogenizer in 9 volumes of cold 0.25 M sucrose containing 0.0033 M Calcium Acetate.

  2. Filter the resulting brei through several layers of cheesecloth and obtain crude nuclear pellets by centrifuging at 3,500 xg for 20 minutes.

  3. Resuspend the nuclear pellet in 80 ml of cold 0.25 Sucrose containing 0.0033 M Calcium Acetate. 4

  4. Obtain three cellulose nitrate centrifuge tubes and place 25 ml. aliquots of the resuspended nuclear pellet in each. Carefully pipette 5.0 ml of 2.0 M Sucrose-0.0033 M Calcium Acetate into the bottom of each tube. Insert a pipette with the 2.0 M sucrose through the suspended nuclei and allow the viscous sucrose to layer on the bottom of the tube. Centrifuge the tubes at 40,000 xg for 60 minutes.

  5. Using the resulting nuclear pellet is just above the dense sucrose layer. It is used to extract chromatin proteins. Carefully remove the supernatant above the pellet with a pipet. Then, insert the pipet through the nuclear layer and remove the bottom sucrose layer. The nuclear pellet will remain in the tube. Resuspend the pellet in 40 ml of 0.075 M NaCl-0.024 M EDTA, pH 8.0 and centrifuge at 7700 xg for 15 minutes.

  6. Remove and discard the supernatant, resuspend the pellet once again in 40 ml of 0.075 M NaCl-0.024 M EDTA, pH 8.0 and centrifuge again at 7700 xg for 15 minutes. Repeat this process one more time.

  7. Resuspend the nuclear pellet in 40 ml of 0.05 M Tris-HCl, pH 8.0 and centrifuge at 7,700 xg for 10 minutes.

  8. Repeat step 7 to thoroughly wash the nuclei and then wash 2x each in 0.01 M Tris pH 8.0, 0.002 M Tris pH 8.0 and 0.0004 M Tris pH 8.0.

  9. Resuspend the final washed nuclear pellet in ice cold distilled water to a final volume of 100 ml and allow to swell overnight at 4° C. Gently stir the mixture on the following day. This solution is the pure chromatin to be used for subsequent analysis.

  10. Determine the purity of the chromatin sample within the nuclear pellet using one of the following:


The extraction of chromatin proteins starts with the isolation of a good nuclear fraction. Nuclear pellets and chromatin should be extracted one day before the laboratory period. If DNA, RNA, and both Histone and Non-Histone proteins are to be separated, begin the procedure approximately three working days prior to lab.

Return to Table of Contents

Cell Biology Laboratory Manual
Dr. William H. Heidcamp, Biology Department, Gustavus Adolphus College,
St. Peter, MN 56082 -- cellab@gac.edu