Application and detection method of circRNA0003307 gene
A gene and gene expression technology, applied in the direction of DNA / RNA fragments, recombinant DNA technology, microbial measurement / inspection, etc., can solve the problem of less circRNA in AS patients, and achieve enrichment of pathogenesis, phosphorylation and nuclear translocation reduction , improve the effect of the pathogenesis
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Embodiment 1
[0020] In order to explore the expression of circRNA0003307 and the expression of regulatory proteins (PI3K, AKT, TNFAIP2 and IL-1β) in peripheral blood mononuclear cells of patients with AS.
[0021] After the project passed the review of the Ethics Committee, the applicant systematically studied the new diagnostic and therapeutic targets of human AS, extracted the peripheral blood of AS patients, extracted PBMCs, and detected the expression of circRNA0003307 gene by real-time PCR.
[0022] In this embodiment, a total of 30 blood samples from patients with active AS and 30 blood samples from healthy people in the control group were collected, a total of 60 samples (see Table 1 for specific information from 30 patients, and Table 2 for sample characteristics).
[0023] Table 1 Sample information
[0024]
[0025]
[0026] Table 2 Sample Characteristics
[0027]
[0028] In this example, 30 cases of AS and 30 cases of healthy control mononuclear cells derived from per...
Embodiment 2c
[0041] Example 2 circRNA0003307 interference sequence and its application
[0042] This example designs and synthesizes its specific interference sequence si-circRNA0003307 (its nucleotide sequence is shown in SEQ ID NO.3) for the full-length sequence of circRNA0003307, and infects synovial fibroblasts to inhibit the circRNA0003307 gene in the cells expression, and further apply the interference gene carrier to regulate the inflammatory response of synovial fibroblasts.
[0043] The specific cell infection method is as follows:
[0044] 1. siRNA transfection steps
[0045] 1) Seed plate, the cell density is 50% suitable.
[0046] 2) The next day (24-36 hours later), the transfection method of each well is as follows:
[0047] A Dissolve 20pmol siRNA in 50ul Opti-mem serum-free medium; B dissolve 1ul lipo2000 in 50ul Opti-mem serum-free medium, mix well and place at room temperature for 5min; C mix tubes A and B and place for 20min.
[0048] 3) During the transfection perio...
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