Coding gene of Mycobacterium tuberculosis H37Rv and use thereof
A technology of Mycobacterium tuberculosis and encoding gene, which can be applied in application, genetic engineering, plant gene improvement and other directions, can solve the problems of wrong gene boundary, cumbersome steps, ribosome translocation, etc., and achieves easy comparison and easy amplification. Effect
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Embodiment 1
[0030] Example 1: Searching for missing annotation coding genes in the H37Rv strain genome
[0031] 1.1 High-coverage proteome verification of the H37Rv strain genome
[0032]A deep coverage study of the proteome was performed on the H37Rv strain using high-coverage proteome technology. Based on the Tuberculosis (20160307) database, the genome was annotated and encoded using the pFind 3 engine. In order to discover new protein coding regions, based on proteomics technology, we used pAnno software to translate the six-reading frame database of H37Rv's genome (NC_000962.3) file published by NCBI, and used this database to perform mass spectrometry data for new peptides. Segments and identification of new proteins. In order to reduce the false positive rate, we used three filtering methods for separately estimating category FDR for annotated peptides and new peptides during the data filtering process, namely S-FDR, T-FDR I and T-FDRII.
[0033] After data analysis, we identifi...
Embodiment 2
[0048] Embodiment 2: Establish the method for identifying MTBC complex group
[0049] (1) Design primers:
[0050] Based on the CDS sequence of the Rv1879c (-|2130001-2130255|) gene shown in SEQ ID NO.1, PCR primers were designed using Oligo7.0. The primer sequences are as follows:
[0051] F: 5'-CCCAGGTAGTGCACACTCAA-3' (SEQ ID NO.4);
[0052] R: 5'-TTACAGGATCGGGTTCTGCT-3' (SEQ ID NO.5)
[0053] The positional relationship between the above two pairs of primers and the Rv1879c (-|2130001-2130255|) gene is shown below, where the subscripts corresponding to the positions of the primers are underlined.
[0054] TAGTCGGCCGATGAAGGCCGGCGACCGGGC CCCCAGGTAGTGCACACTCAA CCCGCCGTCAAGATAGACGTTGTTGAAGGCTTGTGCCAGATAACCGGCTTCTCGTTCGTAGGGATAGCAGTGCAGCAACACGATTGGGGTATTGCCGGACTGCCGCAGGAAGTCGAGCAGATACAGCGGATTGGCCTTGTGCAGATCAGCGTCCCGGTCGCCAAATCCGACGTGGAACTGCAGCGGCTTGCCCAGGCGCAACGCCTGATGCAACCCGAAGC AGCAGAACCCGATCCTGTAA (SEQ ID NO.2)
[0055] (2) Extract the total DNA of the strains to be te...
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