2003PubMedRequires access

[Biological analysis of a novel gene related with interleukin-6].

Rong Xia, Yan Li, Lun-jiang Lin, Jian-nan Feng, Jiong-Cai Lan, Beifen Shen

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Abstract

OBJECTIVE: To understand the action mechanism of interleukin (IL)-6 through investigation of its related genes. METHODS: Using electronic cloning with IL-6-related expressed sequence tags (ESTs), a novel gene at its full length of 924 bp was acquired. Reverse transcriptase-PCR method was subsequently employed to amplify the cDNA of this gene from the total RNA of human U937 cells, which were previously activated with 100 ng/ml IL-6 for 8 h. The fragment was then ligated into the pGEM-Teasy vector and sequence analysis was conducted. RESULT: The whole cDNA gene was successfully fished. CONCLUSION: Electronic cloning technology can be instrumental in identifying novel genes.

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What this paper is about

OBJECTIVE: To understand the action mechanism of interleukin (IL)-6 through investigation of its related genes. METHODS: Using electronic cloning with IL-6-related expressed sequence tags (ESTs), a novel gene at its full length of 924 bp was acquired. Reverse transcriptase-PCR method was subsequently employed to amplify the cDNA of this gene from the total RNA of human U937 cells, which were previously activated with 100 ng/ml IL-6 for 8 h. The fragment was then ligated into the pGEM-Teasy vector and sequence analysis was conducted. RESULT: The whole cDNA gene was successfully fished. CONCLUSION: Electronic cloning technology can be instrumental in identifying novel genes.

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Available abstract

OBJECTIVE: To understand the action mechanism of interleukin (IL)-6 through investigation of its related genes. METHODS: Using electronic cloning with IL-6-related expressed sequence tags (ESTs), a novel gene at its full length of 924 bp was acquired. Reverse transcriptase-PCR method was subsequently employed to amplify the cDNA of this gene from the total RNA of human U937 cells, which were previously activated with 100 ng/ml IL-6 for 8 h. The fragment was then ligated into the pGEM-Teasy vector and sequence analysis was conducted. RESULT: The whole cDNA gene was successfully fished. CONCLUSION: Electronic cloning technology can be instrumental in identifying novel genes.

Key concepts: Complementary DNA, Gene, Cloning (programming), Biology, Sequence analysis, Expressed sequence tag, Molecular biology, Computational biology

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