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中国生物工程杂志

China Biotechnology
China Biotechnology  2022, Vol. 42 Issue (1/2): 80-87    DOI: 10.13523/j.cb.2108008
Orginal Article     
Using Split Green Fluorescent Protein to Detect the Interaction Between Telomerase TERT Subunit and Telomere Terminal Protein TPP1
LI Jiang-bo1,GUO Hong-bin2,WANG Shi-kun3,JIN Rui1,**(),CHENG Long1,**()
1 Department of Medical Molecular Biology, Institute of Biotechnology, Academy of Military Medical Sciences, Academy of Military Sciences, Beijing 100089, China
2 The 361st Regiment Health Team of the Army Frontier Defense, Tibet 859600, China
3 Information and Communication Brigade of Xinjiang Military Region, Tibet 859499, China
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Abstract  

Objective: To construct the eukaryotic expression vector of NGFP-TERT and TPP1-CGFP genes, then verify whether TPP1-CGFP protein can be recruited to the telomere region, and observe the interaction between TERT and TPP1 through the spontaneous reconstruction of GFP protein. Methods: Using the corresponding plasmid as a template, the coding sequences of CDS regions of NGFP, CGFP and TPP1 were amplified by polymerase chain reaction (PCR) technology. NGFP was inserted into the pCDH-Flag-TERT vector by restriction digestion and recombination, and TPP1-CGFP was inserted into the pCDH-Myc-POT1-v5tag vector. After bacterial liquid PCR, vector enzyme digestion and sequencing verification, it was transfected into 293T cells, and its expression was detected by Western blot. Immunofluorescence and telomere Fish were used to verify whether TPP1-CGFP can be recruited to the telomere region. Plasmid co-transformation verified that it can be reassembled into GFP protein. Results: The results of double enzyme digestion showed that the NGFP-TERT and TPP1-CGFP vectors were successfully constructed; the plasmid was extracted and transfected into 293T cells, and Western blot showed that the gene protein was successfully expressed. Immunofluorescence and telomere Fish showed that TPP1-CGFP can be recruited to the telomere region, and plasmid co-transformation can reassemble the split proteins into GFP. Conclusion: The eukaryotic expression vector was successfully constructed and proved that TPP1-CGFP can be recruited to the telomere region, and the split GFP protein can be reassembled by the interaction of connexins and emit green fluorescence. This paper provides a visual cell model for the study of telomerase and TPP1 protein and the interaction of telomeres.



Key wordsSplit GFP      Telomeres      Telomerase      TPP1     
Received: 03 August 2021      Published: 03 March 2022
ZTFLH:  Q814  
Corresponding Authors: Rui JIN,Long CHENG     E-mail: jinr_jin@aliyun.com;biolongcheng@outlook.com
Cite this article:

LI Jiang-bo,GUO Hong-bin,WANG Shi-kun,JIN Rui,CHENG Long. Using Split Green Fluorescent Protein to Detect the Interaction Between Telomerase TERT Subunit and Telomere Terminal Protein TPP1. China Biotechnology, 2022, 42(1/2): 80-87.

URL:

https://manu60.magtech.com.cn/biotech/10.13523/j.cb.2108008     OR     https://manu60.magtech.com.cn/biotech/Y2022/V42/I1/2/80

Fig.1 Pattern picture of vector construction
Fig.2 Electrophoresis of RCR product (target gene) M: BM 2000 DNA marker; 1: TPP1; 2: GFP; 3: CGFP
Fig.3 Picture of the cloning vector pCDH-TPP1-Myc-CGFP,pCDH-Flag-NGFP-TERT bacterial liquid PCR M1: BM 15000 + DNA marker; M2: DL 2000 DNA marker;1: Positive control(TPP1 plasmid); 2: PCDH-TPP1-Myc-CGFP bacterial liquid PCR;4: Positive control (NGFP plasmid); 5: pCDH-Flag-NGFP-TERT bacterial liquid PCR; 3,6: Negative control (DD water)
Fig.4 pCDH-Flag-NGFP-TERT,pCDH-Myc-TPP1-CGFP identified by restriction endonuclease analysis M: BM 2000 DNA marker; 1: Empty vector; 2: Recombinant plasmid pCDH-Flag-NGFP-TERT digested by Nhe I;3: Empty vector; 4: Recombinant plasmid pCDH-Myc-TPP1-CGFP digested by BamHI and NotI
Fig.5 Picture of identifying protein expression
Fig.6 Image of immunofluorescence and telomere colocalization
Fig.7 Picture of the colocalization of TPP1 and telomeres
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