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JCV Case Study

Decent Essays

JCV belongs to the Polyomaviridae family comprising non-enveloped tumor viruses with icosahedral capsids containing small, circular, double-stranded DNA genomes [White et al., 2005]; it encloses a large number of members that are able to infect various animal species including rodents, rabbits, birds and primates, including man [Imperiale, 2001; Delbue et al., 2012]; in particular, to date, have been discovered 11 polyomaviruses infecting man [White et al., 2013; Feltkamp et al., 2013] (Fig. 1.1). The JC human polyomavirus was isolated in 1971 and in the same year it was discovered the polyomavirus human BK (BKV) [Gardner et al., 1971; Padgett et al., 1971]. The transmission is not fully understood. In humans the first site to be infected …show more content…

The human polyomaviruses BK and JC share 75% genomic homology sequence and they are morphologically similar to murine oncogenic polyomavirus (PyV) and they come up a common ancestor to the monkey virus (SV40), whose transformative activity has been associated to human mesothelioma [Frisque et al., 1984; Shah, 2007].
Recently several studies have led to the identification of new family members
Polyomaviridae [White et al., 2013]. In 2007 a molecular screening study that was checking virus in nasopharyngeal drawings of children with respiratory tract infections, led to identification of a new human polyomavirus, called Karolinska Institute Polyomavirus
(KIPyV) (Fig. 1.2). It is phylogenetically related to other human polyomaviruses at the early genomic region level, but has a poor homology of sequence with the genomic region
Late (165). These multifunctional proteins are coded by five different transcripts that are formed in followed by alternative splicing from a single precursor of mRNA. They play precise roles in regulating the virus cycle and in cell transformation.
1.2.3.1 The large T antigen
T-antigen is a protein of 688 amino acids and regulates the transcription of the transcription from early to late proteins as well as replication of the viral genome [Diotti et al., 2013].
In particular, AgT modulates the cellular signaling pathways in such a way as to induce the input of the cell in phase S and activate the replication and transcription apparatus of

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