Molecular marker circRNA for diagnosing idiopathic optic neuritis, kit and application
A molecular marker, optic neuritis technology, applied in DNA/RNA fragments, recombinant DNA technology, microbial determination/inspection, etc., can solve the problems of few circRNAs, no research reports, etc., to achieve good stability, not easy to degrade, The effect of improving the pathogenesis
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Embodiment 1
[0040] Example 1 Establishment of circRNA expression profile in idiopathic optic neuritis
[0041] Sample Collection:
[0042] This study has been approved by the Ethics Committee of the Second Xiangya Hospital of Central South University. All cerebrospinal fluid samples were obtained by lumbar puncture: instruct the patient to take the thoraco-knee position, take the L3 / 4 intervertebral space as the puncture point, routinely disinfect, puncture after layer-by-layer local anesthesia with 2% lidocaine, use a common tube to collect 1ml of cerebrospinal fluid, and freeze it The tubes were aliquoted in 250ul per tube and stored in a -80°C refrigerator within 15 minutes of isolation for circRNA biomarker analysis. Inclusion criteria for the control group: 1. Clinical diagnosis of headache and cause 2. No abnormalities in the head MRI examination. 3. No abnormalities in the biochemical, routine, and three major stainings of the cerebrospinal fluid examination. 4. No ophthalmic dise...
Embodiment 2
[0051] Embodiment 2 qRT-PCR verification
[0052] In the previously established expression profiles, 14 target circRNAs with significant differential expression were selected and verified again in 10 samples by qPT-PCR. The differential expression of the five circRNAs in the cerebrospinal fluid of the two groups was statistically different, and the change trend was consistent with that of the microarray, respectively, hsa_circRNA_0007503 and hsa_circRNA_007630 were up-regulated compared with the control group; hsa_circRNA_406587, hsa_circRNA_054220 and hsa_circRNA_005133 were down-regulated compared with the control group ( image 3 ). Then select the circRNA with statistical difference: hsa_circRNA_0007503 for further verification.
Embodiment 3
[0053] Example 3 Using qRT-PCR to further expand sample size verification
[0054] Expression level of hsa_circRNA_0007503 in cerebrospinal fluid to test its diagnostic value
[0055] Sample collection and total RNA extraction were the same as before.
[0056] cDNA synthesis and qRT-PCR:
[0057] Use RevertAidFirst Strand cDNA Synthesis Kit (Thermofisher) to prepare the reverse transcription system according to the manual for reverse transcription. Reverse transcription products can be stored at -20°C or used immediately. Download the circRNA sequence through the circbase database or UCSC genome browser, and use the primer design software Primer 5.0 to design primers for the target sequence and internal reference sequence. (Table 1) qPCR detection was performed using 2X FastStart Universal SYBR Green Master (Roche). The 96-well plate was placed in a Realtime PCR instrument (StepOnePlusTM Real-Time PCR System, Applied Biosystems) on the reaction. The conditions were 95° C...
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