Method for the detection of cytosine methylations in immobilized DNA samples
A method is described for the analysis of cytosine methylation patterns in genomic DNA samples. In the first method step, the genomic DNA is isolated from cells or other accompanying materials and bound essentially irreversibly to a surface. Then the DNA bound to the surface is treated, preferably with a bisulfite, in such a way that cytosine is converted into a base that is different in its base pairing behavior in the DNA duplex, while 5-methylcytosine remains unchanged. Then the reagents that were used are removed in a washing step. Finally, selected segments of the immobilized DNA are amplified in a polymerase reaction and the amplified products are investigated with respect to their sequence.
1. A method for the conversion of unmethylated cytosine in genomic DNA samples, said method comprising the steps of:
a) isolating the genomic DNA from cells or other accompanying materials and essentially irreversibly immobilizing the isolated genomic DNA to a surface, wherein the immobilization is made on a hydrophobic material, and the immobilization is essentially irreversible only under selected buffer conditions;
b) treating the immobilized DNA with a bisulfite in such a way that cytosine is converted into a base that is different in its base pairing behavior in the DNA duplex, while 5-methylcytosine remains unchanged; and
c) removing the reagents used in step b) in a washing step.
2. The method according to claim 1 , wherein the immobilization of the DNA to the surface is covalent bonding.
3. The method according to claim 1 , wherein the DNA is also isolated directly in the immobilizing step.
4. The method according to claim 3 , wherein the DNA is isolated from whole blood or blood serum.
5. The method according to claim 3 , wherein the DNA is isolated from lysed tissue.
6. The method according to claim 5 , wherein the lysis is conducted by means of proteinase K.
7. The method according to claim 1 , wherein the immobilization is conducted in the wells of a microtiter plate with 96 wells or 384 wells, in which different DNA samples are immobilized in the wells.
8. The method according to claim 1 , wherein the immobilization is conducted in PCR reaction wells, whereby different DNA samples are immobilized in the wells.
9. The method according to claim 1 , wherein the isolating of the DNA occurs on a metal oxide.
10. A method for the conversion of unmethylated cytosine in genomic DNA samples, said method comprising the steps of:
a) isolating the genomic DNA from cells or other accompanying materials and essentially irreversibly immobilizing the isolated genomic DNA to a surface, wherein the immobilization is made on a hydrophobic material, and the immobilization is essentially irreversible only under selected buffer conditions;
b) denaturing the immobilized DNA;
c) treating the immobilized DNA with a bisulfite in such a way that cytosine is converted into a base that is different in its base pairing behavior in the DNA duplex, while 5-methylcytosine remains unchanged; and
d) removing the reagents used in step c) in a washing step,
e) wherein the denaturing step is performed prior to the addition of bisulfite reagent and after having immobilized the DNA to a surface.