Gene methylation and expression
The invention provides a method of analyzing the methylation status of all or part of an entire genome. Moreover, the invention features methods of and reagents for characterizing biological cells containing DNA that is susceptible to methylation. Such methods include methods of diagnosing cancer, e.g., breast cancer.
1. A method of determining, in a human test tissue fibroblast, the level of methylation of one methylation site in a region of the TMEM39A gene, the C7orf3 gene, or the IRX5 gene that is 5′ of the transcription start site, the method comprising
determining the level of methylation of a methylation site in a section of a gene by experimentally assaying, in a test fibroblast from test breast tissue, the degree of methylation of a cytosine residue in a CpG sequence in the section of the gene, wherein
(i) the gene is TMEM39A gene, the section of the gene is 5′ of the transcription start site of the gene, and the CpG sequence is in the AscI restriction site (A) that is in the region of the gene 5′ of the transcription start site of the gene and (B) that was identified by the Methylation Specific Digital Karyotyping (MSDK) tag consisting of SEQ ID NO:621;
(ii) the gene is the C7orf3 gene, the section of the gene is 5′ of the transcription start site of the gene, and the CpG sequence is in the AscI restriction site (A) that is in the region of the gene 5′ of the transcription start site of the gene and (B) that was identified by the MSDK tag consisting of SEQ ID NO:731; or
(iii) the gene is the IRX5 gene, the section of the gene is 5′ of the transcription start site of the gene, and the CpG sequence is in the AscI restriction site (A) that is in the region of the gene 5′ of the transcription start site of the gene and (B) that was identified by the MSDK tag consisting of SEQ ID NO:904.
2. The method of claim 1 , wherein the gene is the TMEM39A gene.
3. The method of claim 1 , wherein the gene is the C7orf3 gene.
4. The method of claim 1 , wherein the gene is the IRX5 gene.