Selective oxidation of 5-methylcytosine by TET-family proteins
The present invention provides for novel methods for regulating and detecting the cytosine methylation status of DNA. The invention is based upon identification of a novel and surprising catalytic activity for the family of TET proteins, namely TET1, TET2, TET3, and CXXC4. The novel activity is related to the enzymes being capable of converting the cytosine nucleotide 5-methylcytosine into 5-hydroxymethylcytosine by hydroxylation.
1. A method comprising contacting with, or delivering to a nucleic acid sequence, an enzyme or fragment thereof that oxidizes at least one methylated DNA base, in an amount effective to convert 5-methylcytosine to 5-hydroxymethylcytosine.
2. The method of claim 1 , wherein the enzyme or fragment thereof comprises a purified and isolated dioxygenase.
3. The method of claim 2 , wherein the purified and isolated dioxygenase comprises a catalytically active TET family enzyme, a functional TET family derivative, a TET catalytically active fragment thereof, or any combination thereof.
4. The method of claim 1 , wherein the contacting with or the delivering to converts a 5-methylcytosine residue in the nucleic acid sequence to a modified base.
5. The method of claim 4 , wherein the modified base is formed by more than one oxidation reaction.
6. The method of claim 4 , wherein the modified base comprises a 5-hydroxymethylcytosine residue.
7. The method of claim 1 , wherein the method comprises contacting the nucleic acid sequence with the enzyme or fragment thereof.
8. The method of claim 1 , wherein the method comprises delivering the enzyme or fragment thereof to the nucleic acid sequence.
9. The method of claim 1 , wherein the nucleic acid sequence is from a somatic cell.