Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/6157
Title: Retroviral vectors and gene therapy: An update
Authors: Maurya, S K
Srivastava, Sushant
Joshi, R K
Keywords: Gene therapy
retroviruses
vector
Issue Date: Oct-2009
Publisher: CSIR
Abstract: Gene therapy aims at treatment of diseases by transfer of genetic material into specific cells of a patient. So the transduction of appropriate target cell is critical. Retroviruses infect nearly every cell in the target population and become integrated in host cell genome for a stable expression. All retroviruses have only three structural genes gag, pol and env, except for lentiviruses where two other genes tat, rev and four accessory genes are required (vif, vpu, nif, vpr). There are two components of retroviral vector system—i) Packaging cell lines, which provide the products of gag, pol & env genes but are unable to package itself as they lack the sequence, and ii) retroviral vectors where gag, pol and env are deleted but sequence along with LTR is present. Several other types of vectors are also described.
Description: 349-357
URI: http://hdl.handle.net/123456789/6157
ISSN: 0975-0967 (Online); 0972-5849 (Print)
Appears in Collections:IJBT Vol.08(4) [October 2009]

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