Leber's hereditary optic neuroretinopathy related mtDNA mutant site integrated detection gene chip, as well as preparation and use thereof
A technology for optic neuropathy and mutation sites, which is applied in the field of gene chip detection to achieve the effects of good clinical promotion value, shortened detection time, and shortened diagnosis time.
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Embodiment 1
[0045] Example 1 Probe Design and Chip Preparation
[0046] (1) Design of probes on the chip:
[0047] According to the 32 LHON-related mtDNA mutation sites and 11719G>A polymorphism sites reported in the MITOMAP database, and referring to the revised Cambridge mtDNA reference sequence (revised Cambridge Reference Sequence, rCRS), 33 pairs of oligonucleotide probes were designed and screened. Needle, so that the Tm value of different probes is located at (45±5) °C as much as possible, the length of the probe is located at 14-20bp, so that the gene locus detected by each pair of probes is located in the middle or near the middle of the probe sequence, so that the probe The binding site to the corresponding single-stranded target gene should be as close as possible between the 5' end and the middle region of the single-stranded target gene to ensure hybridization efficiency. The 5' end of the probe has an amino modification group, so as to combine with the aldehyde group modifi...
Embodiment 2
[0055] Example 2 Mutation detection of samples
[0056] (1) Preparation, labeling and processing of samples:
[0057] DNA extraction kits from Qiagen Company were used to extract DNA from samples from patients with Leber's hereditary optic neuropathy or suspected patients, and set aside.
[0058] PCR amplification and labeling treatment of samples: Under the same thermal cycle, through three sets of multiplex PCR (the nucleotide sequences of ID NO.66-71, ID NO.72-79, ID NO.80-87 were As three sets of multiplex PCR primers) to amplify 11 target genes, these 11 target genes cover 32 mtDNA mutation sites and 11719G>A polymorphism sites related to Leber's hereditary optic neuropathy. In 25ul PCR reaction system (amplification system includes 2.5ul 10*PCR buffer, each 200uM of dATP, dGTP, dCTP, dTTP, 1.5mM MgCl2 , 1.5U DNA TagE (Takara), and primers ranging from 0.05-0.5uM, add 100ng sample DNA to each reaction, and prepare 11 fluorescently labeled sample DNA target fragments thro...
Embodiment 3
[0072] The assembly of embodiment 3 kits
[0073] The gene chip was prepared according to Example 1, and the PCR primers of SEQ ID NO.66-87 recorded in Example 2 were subpackaged, assembled with the prepared gene chip, hybridization solution, and nucleic acid hybridization washing solution, and then packaged to obtain a kit.
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