International Journal of Bioinformatics and Biomedical Engineering
Articles Information
International Journal of Bioinformatics and Biomedical Engineering, Vol.2, No.5, Sep. 2016, Pub. Date: Sep. 10, 2016
Putative Promoters of Two Complete Zika Virus Genome
Pages: 59-64 Views: 4748 Downloads: 1352
Authors
[01] Md. Zakir Hossain, Department of Pharmaceutical Sciences, Biomanufacturing Research Institute and Technology Enterprise (BRITE), North Carolina Central University, Durham, North Carolina, USA.
[02] Rozina Akter, BioMedNano Research Institute, Little Rock, Arkansas, USA.
Abstract
The recent outbreak of Zika virus (ZikaV), which is transmitted through Aedes mosquitoes, is an emerging arbovirus, poses global health concern. Currently, there are no effective vaccinations or proven therapeutics that specifically targets the complete ZikaV genomes. To design an effective antiviral therapeutics for ZikaV, the complete genomes should be targeted along with its possible functions. Since promoters are most important regulatory regions for gene expression, identification of putative promoters are vital. The promoter is a short segment of DNA sequence where RNA polymerase first attaches. It forms a recognition and binding site for the RNA polymerase. In addition, it is asymmetrical and thus indicating the site of initiation and direction of transcription. To date, there is no reported data available for the identification and characterization of promoter sequence in complete ZikaV genomes. By considering the limited data on putative promoter motifs of complete ZikaV genome, our study was designed to identify, characterize and investigate the putative promoter motifs in two complete Zika viral strains (ZikaV isolate SSABR1 and second, Brazil-ZKV2015). In fact, the promoter sequences were identified in both of the two complete ZikaV genomes. Further, the significant promoters name, sequence, weight and locations were also noted. Thus, in silico identification of putative promoter motifs in the two complete ZikaV genomes were studied. Therefore, ZikaV promoters study can be helpful to understand the regulation of ZikaV genes and their functions, which eventually will lead to develop live attenuated ZikaV vaccines and gene therapy.
Keywords
ZikaVirus, Genome, Promoters, Transcription Factors, Vaccines, Gene Therapy
References
[01] Kruger, R. P. (2016). Zika Virus on the move. Cell Leading Edge Select, 164, February 11, 2016.
[02] Faye, O., Freire, C. C., Iamarino, A., Faye, O., de Oliveira, J. V., Diallo, M., et al. (2014). Molecular evolution of Zika virus during its emergence in the 20(th) century. PLoS Negl Trop Dis, 8 (2014), p. e263.
[03] Bogoch, I. I., Brady, O. J., Kraemer, M. U., German, M., Creatore, M. I., Kulkarni, M. A., Brownstein, J. S., Mekaru, S. R., Hay, S. I., Groot, E., Watts, A, Khan, K. (2016) Anticipating the international spread of Zika virus from Brazil. Lancet Jan 14) pii: S0140-6736(16)00080-5.
[04] Campos, G. S. Bandeira, A. C. Sardi, S. I. (2015). Zika virus outbreak, Bahia, Brazil Emerg Infect Dis, 21 (2015), pp. 1885–1886.
[05] Oliveira M. A. S., Malinger, G., Ximenes, R., Szejnfeld, P. O., Sampaio, S. A., Filippis, M. B., (2016). Zika virus intrauterine infection causes fetal brain abnormality and microcephaly: tip of the iceberg? Ultrasound in Obstetrics & Gynecology, 47, pp. 6–7.
[06] Oehler, E., Watrin, L., Larre, P., Leparc-Goffart, I., Lastere, S., Valour, F., et al. (2014). Zika virus infection complicated by Guillain-Barre syndrome--case report, French Polynesia, December 2013, Euro Surveill, 19 (2014), p. 20720.
[07] Petersen E., Wilson M. E., Touch S, McCloskey, B., Mwabae, P. Batese M, Dard, O., Mattes, F., Kidd, M., Ippolitog, G., I. Azharh, E. I., Zumla, A. (2016). Rapid Spread of Zika Virus in the Americas - Implications for Public Health Preparedness for Mass Gatherings at the 2016 Brazil Olympic Games, International Journal of Infectious Diseases, Volume 44, Pages 11–15.
[08] Lewin B, Genes VIII. 2004 pp. 636–637. ISBN 0-13-144946-X.
[09] Prestridge, D. S. (1995). Predicting Pol II Promoter Sequences Using Transcription Factor Binding Sites. J. Mol. Biol. 249: 923-32.
[10] Somvanshi, P., Singh, V., and Seth, P. K., (2008). Identification and analysis of putative promoter motifs in Flavivirus genome, Bioinformation. 3(4): 162–167.
[11] “National Centre for Biotechnology Information”. http://www.ncbi.nlm.nih.gov/nuccore/992324757, May 03, 2016.
[12] “National Centre for Biotechnology Information.” http://www.ncbi.nlm.nih.gov/nuccore/KU497555, May 04, 2016.
[13] “Sciencebuddies”. http://www.sciencebuddies.org/science-fair-projects/project_ideas/Genom_GC_Calculator.shtml, May 02, 2016.
[14] Hiroomi T. (1991). Regulation of JCV promoter function: Evidence that a penta-nucleotide “silencer” repeat sequence AGGGAAGGGA down-regulates transcription of the JC virus late promoter. Virology. 1991; 180: 327.
[15] Shivakumar CV, Das, GC. (1998) The A enhancer of polyomavirus: protein-protein interactions for the differential early and late promoter function under nonreplicating conditions. Intervirology. 1998; 41(2-3): 103-9.
[16] Yoo W, Martin ME, Folk WR. (1991). PEA1 and PEA3 enhancer elements are primary components of the polyomavirus late transcription initiator element. J Virol. 1991 Oct; 65(10): 5391-400.
[17] Hess J, Angel P, Schorpp-Kistner M. 2004AP-1 subunits: quarrel and harmony among siblings. J Cell Sci. Dec 1; 117(Pt 25): 5965-73.
[18] Ghoshal, K., Majumder, S., Jharna, D., Motiwala, T., Bai, S., Sudarshana M. S., Frankel, W., and Jacob. S. T., (2004). Role of Human Ribosomal RNA (rRNA) Promoter Methylation and of Methyl-CpG-binding Protein MBD2 in the Suppression of rRNA Gene Expression. J Biol Chem. Feb 20; 279(8): 6783–6793.
[19] Horan MP, Cooper DN, Upadhyaya M. Hypermethylation of the neurofibromatosis type 1 (NF1) gene promoter is not a common event in the inactivation of the NF1 gene in NF1-specific tumours. Hum Genet. 2000 Jul; 107(1): 33-9.
[20] Kurjogi MM, Sanakal RD, Kaliwal BB. Identification and analysis of putative promoter motifs in bovine herpes virus. Bioinformation. 2012; 8(23): 116770.
[21] Hale TK, Braithwaite AW. The adenovirus oncoprotein E1a stimulates binding of transcription factor ETF to transcriptionally activate the p53 gene. J Biol Chem. 1999 Aug 20; 274(34): 23777-86.
600 ATLANTIC AVE, BOSTON,
MA 02210, USA
+001-6179630233
AIS is an academia-oriented and non-commercial institute aiming at providing users with a way to quickly and easily get the academic and scientific information.
Copyright © 2014 - American Institute of Science except certain content provided by third parties.