Cloning and sequence analysis of chicken interferon-α gene
LI Xiang-rui
Abstract
LI Xiang-rui
Abstract
Chicken interferon-α (ChIFN-α) was amplified from chicken splenic lymphocytes by reverse transcription-polymerase chain reaction (RT-PCR) technique. The cDNA fragment containing coding region of ChIFN-α gene was cloned into the pMD18-T vector and sequenced. The sequence analysis showed that the length of the open reading frame (ORT) was 582 bp. Compared with the ChIFN-α gene sequences available in the GenBank, the homologies of the nucleotide sequences were 98.6%~99.8%. Further analysis of the ChIFN-α gene sequences from different countries and territories showed that the lengths of ORF and encoded amino acids were uniform, and the characters of territory-related changes were not found.
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Chicken interferon-α (ChIFN-α) was amplified from chicken splenic lymphocytes by reverse transcription-polymerase chain reaction (RT-PCR) technique. The cDNA fragment containing coding region of ChIFN-α gene was cloned into the pMD18-T vector and sequenced. The sequence analysis showed that the length of the open reading frame (ORT) was 582 bp. Compared with the ChIFN-α gene sequences available in the GenBank, the homologies of the nucleotide sequences were 98.6%~99.8%. Further analysis of the ChIFN-α gene sequences from different countries and territories showed that the lengths of ORF and encoded amino acids were uniform, and the characters of territory-related changes were not found.
Key concepts: GenBank, Open reading frame, Gene, Biology, Coding region, Genetics, Complementary DNA, Sequence analysis