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  5. Designing DNA probe from human Papillomavirus (HPV) 58 in E6 region as biosensing element for development of biosensor
 
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Designing DNA probe from human Papillomavirus (HPV) 58 in E6 region as biosensing element for development of biosensor

Journal
AIP Conference Proceedings
ISSN
0094243X
Date Issued
2024-03-21
Author(s)
Jaapar N.F.
Nor Azizah Parmin
Universiti Malaysia Perlis
Halim N.H.A.
Uda Hashim
Universiti Malaysia Perlis
Subash Chandra Bose Gopinath
Universiti Malaysia Perlis
Ruslinda A. Rahim
Universiti Malaysia Perlis
Nadzirah S.
Voon Chun Hong
Universiti Malaysia Perlis
Muhammad Nur Aiman Uda
Universiti Malaysia Perlis
Ang W.C.
Zakaria I.I.
Rejali Z.
Afzan A.
Hamzah A.A.
Dee C.F.
Halim F.S.
DOI
10.1063/5.0148563
Abstract
Globally, second leading cause of death for women is a Cervical Cancer. CC is caused by infection of Human Papillomavirus (HPV). HPV strains 16 (50.8%), 18 (17.6%), and 58 (2.6%) became the most leading strains of infection in Malaysia. Recently, a study showed that HPV 58 was rare worldwide but famous in Asia countries including Malaysia. However, detection the significance of HPV-58 in women has not been studied extensively because of rare case compared to HPV 16 and 18. HPV-58 is commonly found in East Asia, but infrequently worldwide, due to changes in the environment of viruses and humans. Detailed biological knowledge is crucial for the development of effective countermeasures, diagnostic tests, vaccines and antiviral drugs against the HPV. The oligonucleotide sequences of HPV 58 in E6 region have been analysed between 24-35 mer in order to maintain the specificity and selectivity. The percentage of similarities between the coding sequences has developed with 66.7% of GC content. The DNA probe of HPV 58 was 5'GGG CGC TGT GCA GTG TGT TGG AGA CCC CGA3' with 30 mer of oligonucleotides. The important of E6 region for developing the coding sequence as it involved in the DNA reproduction, transcription, translation regulation and transformation of HPV genome. Phylogenetic trees were then constructed by Neighbour-Joining and the Kimura 2-parameters methods, followed by an analysis of selection pressures acting on the E6/E7 genes by ebi ac uk tools.
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