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The expression and bioinformatic analysis of a novel gene C20orf14 associated with lymphoma

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Summary

The aim of the present study was to explore the differentially expressed genes in the blood vessel endothelial cells (BVECs) between diffuse large B-cell lymphoma (DLBCL) and reactive lymph node hyperplasia (RLNH), and to perform an initial bioinformatics analysis on a novel gene, C20orf14, which is highly expressed in lymph node of lymphoma. The mRNA of the tissue from the BVECs of DLBCL and RLNH tissues was labeled with biotin respectively and hybridized with expression profile microarray, and the differentially expressed genes were obtained. Initial bioinformatics analysis was performed on a novel gene named C20orf14. Its gene structure, genomic localization, the physical and chemical characteristics of the putative protein, subcellular localization, functional domain etc. were predicted, and the systematic evolution analysis was performed on the similar proteins among several species. By using expression profile microarray, many differentially expressed genes were uncovered. The efficient bioinformatics analysis have fundamentally identified that C20orf14 was a nuclear protein, and may be involved in the post-transcription modification of mRNA. Therefore, microarray is an efficient and high throughout strategy for the detection of differentially expressed genes, and C20orf14 is thought to be a potential target for tumor metastasis researches by bioinformatics analysis.

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Correspondence to Liangping Su  (苏良平).

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Liangping SU, male, born in 1964, Doctorial Candidate

This project was supported by grants from National “973” Key Basic Research and Development Program Foundation (No. 2002CB513100) and the transversal project of Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology (No. 2007004) of China.

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Su, L., Chen, D., Zhang, J. et al. The expression and bioinformatic analysis of a novel gene C20orf14 associated with lymphoma. J. Huazhong Univ. Sci. Technol. [Med. Sci.] 28, 97–101 (2008). https://doi.org/10.1007/s11596-008-0125-6

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  • DOI: https://doi.org/10.1007/s11596-008-0125-6

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