Cloning and Sequencing of Glycoprotein Gene of Chinese Rabies Vaccine Strain CTN-1-V
Dong Guan-mu
Abstract
Dong Guan-mu
Abstract
Objective To study the structure of glycoprotein (GP) gene of Chinese rabies vaccine strain CTN-1-V. Methods Amplify the full-length cDNA fragment of GP from the Vero cells infected with CTN- 1-V strain by RT-PCR and clone into PCR2.1 vector for sequencing. Results The cDNA of GP of CTN-1-V strain consisted of 1 575 nucleic acids encoding 524 amino acids. The homologies of nucleic acid and ami-no acid sequences to those reported abroad were 80.8%-92.4% and 82.9%-93.3% respectively. Conclusion The study provided a theoretical basis for selecting a candidate vaccine strain.
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Objective To study the structure of glycoprotein (GP) gene of Chinese rabies vaccine strain CTN-1-V. Methods Amplify the full-length cDNA fragment of GP from the Vero cells infected with CTN- 1-V strain by RT-PCR and clone into PCR2.1 vector for sequencing. Results The cDNA of GP of CTN-1-V strain consisted of 1 575 nucleic acids encoding 524 amino acids. The homologies of nucleic acid and ami-no acid sequences to those reported abroad were 80.8%-92.4% and 82.9%-93.3% respectively. Conclusion The study provided a theoretical basis for selecting a candidate vaccine strain.
Key concepts: Complementary DNA, Nucleic acid, Strain (injury), Cloning (programming), Rabies vaccine, Gene, Virology, Biology