Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/15934
Title: Cloning and expression analysis of multiple proteins encoding P gene of Newcastle disease virus
Authors: Kumar, Rajiv
Tiwari, Ashok K
Chaturvedi, Uttara
Kumar, G. Ravi
Sahoo, A P
Keywords: Annexin V assay;In vitro expression;Newcastle disease virus;P gene;RNA editing;Viral gene oncotherapy
Issue Date: Feb-2013
Publisher: NISCAIR-CSIR, India
Abstract: Viral gene oncotherapy is emerging as a biotherapeutic cancer treatment modality based on targeted killing of cancer cells by viral genes. Newcastle disease virus (NDV) has the property to cause selective oncolysis of tumor cells sparing normal cells. NDV has a single stranded negative sense RNA genome, which is 15,186 nucleotide long and consists of six genes, which codes for eight proteins. NDV like other paramyxoviruses has the ability to generate multiple proteins from the P gene. P protein is encoded by an unedited transcript of the P gene, whereas the V and W protein are the results of RNA editing event in which one and two G residues are inserted at a conserved editing site within the P gene mRNA resulting in V and W transcripts, respectively. Although NDV is known to cause oncolysis by triggering apoptosis, the role of different viral proteins in selective oncolysis is still unclear. P gene edited products are known for its anti-apoptotic property in homologous host. In the present study, NDV P gene and its RNA edited products were amplified, cloned, sequenced and in vitro expression was done in HeLa cells. Further constructs were assayed for their apoptosis inducing ability in HeLa cells. Preliminary study suggested that P, V and W proteins are not apoptotic to HeLa cells.
Page(s): 116-123
URI: http://hdl.handle.net/123456789/15934
ISSN: 0975-1009 (Online); 0019-5189 (Print)
Appears in Collections:IJEB Vol.51(02) [February 2013]

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