» Articles » PMID: 3024171

Nondefective Spleen Necrosis Virus-derived Vectors Define the Upper Size Limit for Packaging Reticuloendotheliosis Viruses

Overview
Specialty Science
Date 1986 Dec 1
PMID 3024171
Citations 20
Authors
Affiliations
Soon will be listed here.
Abstract

We constructed a nondefective retrovirus vector based on spleen necrosis virus (SNV), a replication-competent reticuloendotheliosis virus. We introduced different DNA sequences into this vector and studied the ability of the resulting viruses to replicate in chicken embryo fibroblasts. The replication efficiency of SNV-derived viruses decreased with increasing virus size. Viruses larger than 9.4 kilobases (kb) were rapidly overgrown by replication-competent deletion mutants. The size restriction for the efficient replication of nondefective SNV-derived viruses prevented the production of viruses larger than 10.0 kb. Analysis of the kinetics of virus particle release indicated that the size restriction occurred during virus encapsidation.

Citing Articles

The impact of lentiviral vector genome size and producer cell genomic to gag-pol mRNA ratios on packaging efficiency and titre.

Sweeney N, Vink C Mol Ther Methods Clin Dev. 2021; 21:574-584.

PMID: 34095341 PMC: 8141603. DOI: 10.1016/j.omtm.2021.04.007.


Dual Targeting to Overcome Current Challenges in Multiple Myeloma CAR T-Cell Treatment.

van der Schans J, van de Donk N, Mutis T Front Oncol. 2020; 10:1362.

PMID: 32850436 PMC: 7419675. DOI: 10.3389/fonc.2020.01362.


A review of emerging physical transfection methods for CRISPR/Cas9-mediated gene editing.

Fajrial A, He Q, Wirusanti N, Slansky J, Ding X Theranostics. 2020; 10(12):5532-5549.

PMID: 32373229 PMC: 7196308. DOI: 10.7150/thno.43465.


Generation of High-Titer Self-Inactivated γ-Retroviral Vector Producer Cells.

Ghani K, Boivin-Welch M, Roy S, Dakiw-Piaceski A, Barbier M, Pope E Mol Ther Methods Clin Dev. 2019; 14:90-99.

PMID: 31312667 PMC: 6610700. DOI: 10.1016/j.omtm.2019.05.013.


Inducible Genome Editing with Conditional CRISPR/Cas9 Mice.

Katigbak A, Robert F, Paquet M, Pelletier J G3 (Bethesda). 2018; 8(5):1627-1635.

PMID: 29519936 PMC: 5940154. DOI: 10.1534/g3.117.300327.


References
1.
Watanabe S, Temin H . Construction of a helper cell line for avian reticuloendotheliosis virus cloning vectors. Mol Cell Biol. 1983; 3(12):2241-9. PMC: 370095. DOI: 10.1128/mcb.3.12.2241-2249.1983. View

2.
Tarpley W, Temin H . The location of v-src in a retrovirus vector determines whether the virus is toxic or transforming. Mol Cell Biol. 1984; 4(12):2653-60. PMC: 369274. DOI: 10.1128/mcb.4.12.2653-2660.1984. View

3.
Rigby P . Cloning vectors derived from animal viruses. J Gen Virol. 1983; 64 (Pt 2):255-66. DOI: 10.1099/0022-1317-64-2-255. View

4.
Hirt B . Selective extraction of polyoma DNA from infected mouse cell cultures. J Mol Biol. 1967; 26(2):365-9. DOI: 10.1016/0022-2836(67)90307-5. View

5.
Weil J, deWein N, Casale A . Morphogenesis of lambda with genomes containing excess DNA: functional particles containing 12 and 15 per cent excess DNA. Virology. 1975; 63(2):352-66. DOI: 10.1016/0042-6822(75)90309-8. View