Method Article

Chromatin Shearing: A Method to Generate Chromatin Fragments Using Enzymatic Digestion

April 30th, 2023

In This Article

Abstract

Loading...
$$\rightleftharpoonup{xx}$$ $$\longleftharp{xx}$$, $$\longrightharp{xx}$$,

Source: Fuchs, A. R. et al. A Chromatin Immunoprecipitation Assay to Identify Novel NFAT2 Target Genes in Chronic Lymphocytic Leukemia. J. Vis. Exp.(2018).

This video describes the protocol for chromatin shearing using micrococcal nuclease enzymatic digestion. Chromatin shearing is an essential step in Chromatin immunoprecipitation or ChIp workflow, which helps investigate protein-DNA interaction in human chronic myeloid leukemia cells. In the feature protocol chromatin shearing is performed using sonication.

Protocol

Loading...
$$\rightleftharpoonup{xx}$$ $$\longleftharp{xx}$$, $$\longrightharp{xx}$$,

1. Fixation, Cell Lysis, and Chromatin Shearing

NOTE: Patient samples and Jurkat cells are fixed and lysed with a commercially available ChIP kit according to the manufacturer's instructions with modifications as described previously. The fixation is performed under a laminar flow hood.

  1. Prepare a 1.5 mL tube with 1 mL of 37% formaldehyde, a 1.5 mL tube with 1 mL of 1.25 M glycine, a 5 mL tube with 4 mL of 1x PBS and a box with ice for the fixation of the cells.
  2. After stimulation of the cells for the respective incubation time, Stimulate the cells by adding 32.4 nM phorbol 12-myrist....

Access restricted. Please log in or start a trial to view this content.

Results

Loading...
$$\rightleftharpoonup{xx}$$ $$\longleftharp{xx}$$, $$\longrightharp{xx}$$,

Western blot results; NFAT2 and GAPDH protein analysis; comparison between manufacturers.
Figure 1: Examples of antibody performance in fixed Jurkat cells assessed by SDS-PAGE and Western-Blot. (a) Jurkat cells were fixed for 0 min (bands A and D), 2.5 min (bands B and E), or 5 min (C and F) and the αNFAT2-.......

Access restricted. Please log in or start a trial to view this content.

Disclosures

Loading...
$$\rightleftharpoonup{xx}$$ $$\longleftharp{xx}$$, $$\longrightharp{xx}$$,
No conflicts of interest declared.

Materials

List of materials used in this article
NameCompanyCatalog NumberComments
37 % Formaldehyde p.a., ACSRoth4979.1
1 X PBSSigma AldrichD8537
1.5 mL tube shaker Themomixer comfortEppendorf5355 000.011Can be substituted with similar instruments
M220 Focused-ultrasonicatorCovaris500295
20X Bolt MES SDS Running BufferThermo ScientificB0002
Tris Buffered Saline (TBS-10X)Cell Signaling#12498
iBlot 2 Gel Transfer Device Thermo ScientificIB21001
iBlot 2 Transfer Stacks, nitrocellulose, regular sizeThermo ScientificB23001
big CentrifugeEppendorf5804RCan be substituted with similar instruments
DNA LoBind Tube 1.5 mLeppendorf22431021
Halt Protease and Phosphatase Inhibitor Cocktail (100X)Thermo Scientific78440
Small CentrifugeThermo ScientificHeraeus Fresco 17
Density gradient medium Biocoll (Density 1,077 g/ml)MerckL 6115

Reprints and Permissions

Request permission to reuse the text or figures of this JoVE article

Request Permission

Tags

Micrococcal NucleaseSonicationChromatin ImmunoprecipitationDNA Fragment AnalysisFormaldehyde Cross linkingCell LysisTBE Agarose GelFocused UltrasonicatorChronic Myeloid Leukemia

Related Articles