Restriction Maps of Five Autographa californica MNPV Variants, Trichoplusia ni MNPV, and Galleria mellonella MNPV DNAs with Endonucleases SmaI, KpnI, BamHI, SacI, XhoI, and EcoRI.
Gale E. Smith,Max D. Summers +1 more
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TLDR
The restriction sites of Autographa californica nuclear polyhedrosis virus E2 DNA were mapped for the endonucleases SmaI, KpnI, BamHI, SacI, XhoI, and EcoRI to identify distinct AcMNPV variants, Trichoplusia ni, and Galleria mellonella genomes, which were distinct but with very similar genomes and protein structures.Abstract:
The restriction sites of Autographa californica nuclear polyhedrosis virus (Ac M NPV) E2 DNA were mapped for the endonucleases Sma I, Kpn I, Bam HI, Sac I, Xho I, and Eco RI. The restriction maps of four other Ac M NPV variants, Trichoplusia ni (Tn M NPV), and Galleria mellonella (Gm M NPV) genomes were determined and compared to the endonuclease cleavage maps of Ac M NPV E2 DNA. The viral structural polypeptides of Ac M NPV variants S3, E2, S1, M3, and R9 were the same when analyzed by polyacrylamide gel electrophoresis. The major structural polypeptides of Gm M NPV and Tn M NPV had the same pattern in polyacrylamide gels as did Ac M NPV structural polypeptides. Gm M NPV and Tn M NPV had several minor structural protein differences as compared with Ac M NPV. Ac M NPV variants, Tn M NPV, and Gm M NPV were distinct but with very similar genomes and protein structures. Imagesread more
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Trends in the development of baculovirus expression vectors
Verne A. Luckow,Max D. Summers +1 more
TL;DR: The current status and potential use of baculovirus vectors for the expression of foreign genes in insect cells are described and are contributing to understanding the molecular biology of gene and protein function and regulation in both vertebrate and insect systems.
Journal ArticleDOI
Efficient generation of infectious recombinant baculoviruses by site-specific transposon-mediated insertion of foreign genes into a baculovirus genome propagated in Escherichia coli.
TL;DR: This work has shown that a novel baculovirus shuttle vector that can replicate in Escherichia coli as a plasmid and can infect susceptible lepidopteran insect cells by using a novel recombinant virus that contains a mini-F replicon, a kanamycin resistance marker, and attTn7, the target site for the bacterial transposon Tn7.
Journal ArticleDOI
The bidirectional transfer of DNA and RNA to nitrocellulose or diazobenzyloxymethyl-paper
Gale E. Smith,Max D. Summers +1 more
TL;DR: DNA fragments from 5% polyacrylamide gels were efficiently blotted after 36 h onto nitrocellulose filters using bidirectional transfer and were shown to be efficient substrates for homologous [32P]DNA probes.
Patent
Method for producing a recombinant baculovirus expression vector
Gale E. Smith,Max D. Summers +1 more
TL;DR: In this paper, a method for producing a recombinant baculovirus expression vector, capable of expressing a selected gene in a host insect cell, is disclosed. But this method requires the use of a modified cloning vehicle.
Journal ArticleDOI
Molecular Engineering of the Autographa californica Nuclear Polyhedrosis Virus Genome: Deletion Mutations Within the Polyhedrin Gene
TL;DR: A method to introduce site-specific mutations into the genome of Autographa californica nuclear polyhedrosis virus demonstrated that the polyhedrin gene was not essential for the production of infectious virus and that deletion of certain sequences within the gene did not alter the control, or decrease the level of expression, ofpolyhedrin.
References
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Journal ArticleDOI
Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4
TL;DR: Using an improved method of gel electrophoresis, many hitherto unknown proteins have been found in bacteriophage T4 and some of these have been identified with specific gene products.
Journal Article
Cleavage of structural proteins during the assemble of the head of bacterio-phage T4
TL;DR: Using an improved method of gel electrophoresis, many hitherto unknown proteins have been found in bacteriophage T4 and some of these have been identified with specific gene products as mentioned in this paper.
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Labeling deoxyribonucleic acid to high specific activity in vitro by nick translation with DNA polymerase I
TL;DR: Labeled DNAs (and restriction endonuclease fragments derived from them) are useful probes for detecting rare homologous sequences by in situ hybridization and reassociation kinetic analysis.
Journal ArticleDOI
Restriction endonucleases in the analysis and restructuring of dna molecules.
Daniel Nathans,Hamilton O. Smith +1 more
Journal ArticleDOI
Analysis of baculovirus genomes with restriction endonucleases.
Gale E. Smith,Max D. Summers +1 more
TL;DR: Isolation of variants from the three phenotypic forms has shown that each of the infectious forms is heterogeneous and that no segregation of genotypes among the three forms was evident.
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