DocumentCode :
619341
Title :
Identifying hsa-miR-122 target sites in HCV isolate JFH-1
Author :
Sim-Hui Tee ; Quek, Albert
Author_Institution :
Multimedia Univ., Cyberjaya, Malaysia
fYear :
2013
fDate :
7-9 April 2013
Firstpage :
863
Lastpage :
868
Abstract :
MicroRNAs are short regulatory genes that regulate the gene expression in various cellular activities and pathways. Identification of microRNA target site is important for the understanding of pathogenesis and cellular functions. This study applies a computational approach to identify hsa-miR-122 target sites in hepatitis C virus isolate JFH-1. The minimum free energy, seed region complementarity, and 3´ region complementarity were taken as the determining factors for the binding affinity. We have identified a total of four hsa-miR-122 target sites. The identified target sites can be used in therapy strategies and drug designs for hepatocellular carcinoma and hepatitis C.
Keywords :
RNA; cellular biophysics; free energy; genetics; microorganisms; molecular biophysics; 3´ region complementarity; HCV iusolate; JFH-1; binding affinity; cellular activities; cellular functions; computational approach; drug designs; gene expression; hepatitis C virus; hepatocellular carcinoma; hsa-miR-122 target site identification; microRNAs; minimum free energy; pathogenesis; pathways; seed region complementarity; short regulatory genes; therapy strategies; Bioinformatics; Cancer; DNA; Immune system; Lungs; RNA; Viruses (medical); bioinformatics; hepatitic C virus; microRNA;
fLanguage :
English
Publisher :
ieee
Conference_Titel :
Business Engineering and Industrial Applications Colloquium (BEIAC), 2013 IEEE
Conference_Location :
Langkawi
Print_ISBN :
978-1-4673-5967-2
Type :
conf
DOI :
10.1109/BEIAC.2013.6560259
Filename :
6560259
Link To Document :
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