[Cloning and identification of the cDNA and genomic DNA sequences of the defensin gene of anopheles sinensis].
Ya-jing Zhang, Xiaoguang Chen, Xue-li Zheng, Chunmei Wang
Abstract
Ya-jing Zhang, Xiaoguang Chen, Xue-li Zheng, Chunmei Wang
Abstract
OBJECTIVE: To clone and identify the cDNA sequence and genomic DNA sequence of Anopheles sinensis defensin gene. METHODS: Referring to the published defensin gene sequences of Aedes aegypti and Anopheles gambiae, pairs of primers were designed to amplify the cDNA sequence and genomic DNA sequence of Anopheles sinensis defensin gene with template of Anopheles sinensis total RNA by RT-PCR and genomic DNA by nested PCR, respectively. These amplified fractions were cloned and sequenced, and were further identified and analyzed by relevant bioinformatics softwares. RESULTS: Complete genomic DNA sequence was cloned, including 5' and 3' UTR fraction and two exons separated by a 85 bp intron. Besides, the whole cDNA sequence of Anopheles sinensis defensin gene with 324 bp was also cloned, and its ORF encoded 107 amino acids. The mature peptide had 40 amino acids residues. CONCLUSION: The whole cDNA sequence and complete genomic DNA sequence of the defensin gene of Anopheles sinensis have been cloned and identified for the first time.
OpenAlex reports 2 citations for this work. Citation counts describe recorded attention and do not establish research quality.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
OBJECTIVE: To clone and identify the cDNA sequence and genomic DNA sequence of Anopheles sinensis defensin gene. METHODS: Referring to the published defensin gene sequences of Aedes aegypti and Anopheles gambiae, pairs of primers were designed to amplify the cDNA sequence and genomic DNA sequence of Anopheles sinensis defensin gene with template of Anopheles sinensis total RNA by RT-PCR and genomic DNA by nested PCR, respectively. These amplified fractions were cloned and sequenced, and were further identified and analyzed by relevant bioinformatics softwares. RESULTS: Complete genomic DNA sequence was cloned, including 5' and 3' UTR fraction and two exons separated by a 85 bp intron. Besides, the whole cDNA sequence of Anopheles sinensis defensin gene with 324 bp was also cloned, and its ORF encoded 107 amino acids. The mature peptide had 40 amino acids residues. CONCLUSION: The whole cDNA sequence and complete genomic DNA sequence of the defensin gene of Anopheles sinensis have been cloned and identified for the first time.
Key concepts: Biology, genomic DNA, Complementary DNA, Genetics, Gene, Anopheles sinensis, Sequence analysis, Molecular biology