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