Expression of a truncated retroviral envelope gene enhances expression of normal cellular phenotypes.

Abstract:

:The envelope gene of Moloney murine leukemia virus (Mo-MLV) and its various functional domains have been studied extensively but not as much in terms of their biological effects on cell growth. In this study, we report the biological characterization of a truncated Mo-MLV envelope gene, LN11, which is devoid of a signal peptide. Its expression in various cell types, as compared to the control, enabled the transduced cells to assume a more normal phenotype, which is defined by an increase in contact inhibition and factor dependence, as well as reduced tumorigenicity. LN11-transduced fibroblasts exhibited a higher degree of contact inhibition, assumed a more flattened morphology and were more adherent compared to the control. In v-abl transformed hematopoietic cells, expression of LN11 resulted in slower cell growth, which was due to an enhanced dependence on exogenous growth factors. Enforced expression of LN11 also resulted in a slower rate of tumor development and a reduced tumor load. Thus, modification of a retroviral genome could have a significant impact on cell growth and development. This is one example where we need to consider the safety issue carefully when constructing retrovirus vectors for gene therapy.

journal_name

J Biomed Sci

authors

Chen H,Chung SW,Wong PM

doi

10.1007/BF02253367

keywords:

subject

Has Abstract

pub_date

2000-11-01 00:00:00

pages

514-22

issue

6

eissn

1021-7770

issn

1423-0127

pii

25487

journal_volume

7

pub_type

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