Histone methylation is an important epigenetic modification that plays important roles in plant development and growth. Histone methytransferases are the enzymes to establish histone methylation and here we describe a simple and effective protocol for detecting methyltransferase activity and specificity in vitro.
Mononuclosomes and Oligonucleosomes (see procedure)
Coomassie brilliant blue R-250
MiliQ water
SDS-PAGE
KCl
MgCl2
Sucrose
ZnCl2
β-mercaptoethanol
MAB buffer (see Recipes)
Equipment
Water bath
Procedure
Substrate Purified recombinant Histones (Ding et al., 2007), histone H3, core histones, mononuclosome and oligonucleosome (from Hela cells or recombinant ones from E.coli). Note: The mononucleosomes and oligonucleosomes prepared from Hela cells were gifts from Yi Zhang (UNC Chapel Hill, USA). The recombinant oligonucleosomes from E. coli were gifts from Bing Zhu (NIBS, Beijing, China).
Reaction A mixture containing 1-5 μl enzyme (such as SDG725), 5 μl 4x MAB buffer, 250 nCi 14C labeled SAM and 1 μg substrates to 20 μl volume, is kept at 37 °C for 1-2 h. The reaction is stopped by adding 5 μl 5x SDS-PAGE loading buffer and boiling at 100 °C for 5 min, and 5 μl samples will be analyzed by 15% SDS-PAGE gel electrophoresis and visualized by Coomassie brilliant blue R-250. The SDS-PAGE gel is dried and exposed to X-ray films or scanned by Typhoon (GE) (15% refers to the concentration of Acr/Bis. Different histones can be separated more clearly by 15% SDS-PAGE).
Recipes
MAB buffer 1x MAB buffer 50 mM Tris-Cl (pH 8.5) 20 mM KCl 10 mM MgCl2 250 mM Sucrose 100 μM ZnCl2 10 mM β-mercaptoethanol
Acknowledgments
The protocol was adapted from previously published papers (Rea et al., 2000; Ding et al., 2007).
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