Integrated purification and measurement of dna methylation and co-measurement of mutations and/or mrna expression levels in automated reaction cartridge

A technology of methylation and reaction box, which is applied in the direction of DNA preparation, recombinant DNA technology, microbial measurement/testing, etc.
CN107922941APending Publication Date: 2018-04-17CEPHEID INC

Patent Information

Authority / Receiving Office
CN · China
Current Assignee / Owner
CEPHEID INC
Publication Date
2018-04-17

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Abstract

In various embodiments methods of determining methylation of DNA are provided. In one illustrative, but non-limiting embodiment the method comprises i) contacting a biological sample comprising a nucleic acid to a first matrix material comprising a first column or filter where said matrix material binds and / or filters nucleic acids in said sample and thereby purifies the DNA; ii) eluting the boundDNA from the first matrix material and denaturing the DNA to produce eluted denatured DNA; iii) heating the eluted DNA in the presence of bisulfite ions to produce a deaminated nucleic acid; iv) contacting said deaminated nucleic acid to a second matrix material comprising a second column to bind said deaminated nucleic acid to said second matrix material; v) desulfonating the bound deaminated nucleic acid and / or simultaneously eluting and desulfonating the nucleic acid by contacting the deaminated nucleic acid with an alkaline solution to produce a bisulfite converted nucleic acid; vi) eluting said bisulfite converted nucleic acid from said second matrix material; and vii) performing methylation specific PCR and / or nucleic acid sequencing, and / or high resolution melting analysis (HRM) onsaid bisulfite-converted nucleic acid to determine the methylation of said nucleic acid, wherein at least steps iv) through vi) are performed in a single reaction cartridge.
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Description

[0001] Cross References to Related Applications

[0002] This application claims priority to and benefit of USSN 62 / 175,916 filed June 15, 2015, which is hereby incorporated by reference in its entirety for all purposes.

[0003] statement of government support

[0004] [Not applicable] Background technique

[0005] The genomes of higher eukaryotes contain modified 5-methylcytidine (5-meC). This modification usually occurs as part of a dinucleoside CpG in which cytosine is converted to 5-methylcytosine in a reaction that involves flipping a target cytosine out of the full double helix And the methyl group is transferred from S-adenosylmethionine by methyltransferases (see, eg, Klimasauskas et al. (1994) Cell 76:357-369). This enzymatic conversion is the major DNA epigenetic modification known to occur in vertebrates and is essential for normal embryonic development (see, e.g., Bird (1992) Cell 70:5-8; Laird and Jaenisch ( 1994) Human Mol. Genet. 3:1487-1495; and Li et al. ...

Claims

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