Microinjected simian virus 40 cRNA is spliced, as evidenced by electron microscopy.

1983 ◽  
Vol 48 (1) ◽  
pp. 296-299 ◽  
Author(s):  
M Graessmann ◽  
A Graessmann ◽  
H Westphal
Author(s):  
Pierre Oudet ◽  
Patrick Schultz ◽  
Jean-Claude Homo ◽  
Pierre Colin

2007 ◽  
Vol 353 (2) ◽  
pp. 424-430 ◽  
Author(s):  
Vered Roitman-Shemer ◽  
Jitka Stokrova ◽  
Jitka Forstova ◽  
Ariella Oppenheim

Author(s):  
Ronald Glaser ◽  
Ross Farrugia

Several laboratories have reported that simian virus 40 (SV40) was rescued from transformed cells when the nonproducing cells were cocultivated or fused in the presence of ultraviolet inactivated Sendai virus (UV-SV), to potentially susceptible cells. Evidence obtained from studies in which nuclei from heterokaryons were isolated and separated on density gradients, indicated that rescued virus was first detected in the transformed nuclei of the heterokaryons formed during cell fusion. The present study was performed to determine how long after fusion SV40 virus particles could be found in the nuclei of the heterokaryons and to investigate the site of rescue by electron microscopy.


Author(s):  
T. S. Baker ◽  
J. Drak ◽  
M. Bina

The discovery that the T=7 icosahedral capsid of polyoma virus is composed of 72 pentameric capsomers rather than 12 pentamers and 60 hexamers as predicted by constraints of quasi-equivalence has prompted an examination of SV40 virus by electron microscopy to determine whether the capsids of other members of the papovavirus family are similarly constructed.Thin layers of buffered aqueous solutions (∼4 mg/ml) of Simian virus 40 (strain WT776) were prepared for cryo-microscopy using recently developed procedures. Images of virus particles suspended in thin layers of vitreous ice over holes in the carbon support film and maintained at -170°C were recorded using minimal irradiation conditions. Figure 1 shows a typical field in which the frozen solution is similar in thickness to the virus particles (∼49 nm diameter). Particles appear to be excluded or squeezed away from the thinnest regions of solution (e.g., the clear region bordered by particles at the top of Fig. 1).


Author(s):  
T.S. Baker ◽  
N. H. Olson ◽  
W. W. Newcomb ◽  
J. C. Brown ◽  
C. Olson

Bovine papilloma virus type 1 (BPV-1) is a member of the papillomavirus genus, one of two in the Papovaviridae family. Papovaviruses are characterized by similarities in their capsid structure, genetics, biochemical composition and role in the formation of benign and cancerous tumors. The discoveries that the capsid structures of polyoma and simian virus 40 (SV40) (members of the genus polyomavirus) consist of 72 pentameric capsomeres raises the fundamental question of whether or not the capsids of the larger and more complex papilloma viruses have a similar, unexpected arrangement of the capsid subunits. The recent development of cryo-electron microscopy techniques, which facilitate direct visualization of the “native” morphology of biological specimens at moderate resolution (1-4 nm), provides an opportunity to critically examine the structure of BPV-1.The BPV-1 used in this study was originally isolated from a calf in 1965, passaged again in 1986, and stored in 50% glycerin and phosphate buffered saline. Virus was extracted and purified following the protocol of Cowsert et al. (1987): epithelial tissue rich in BPV-1 was mixed with an equal volume of buffer (1M NaCl, 20mM Tris, pH 7.5) and disrupted in a Waring blender. After high speed clarification, the supernatant fraction was mixed with an equal volume of Freon 113 and centrifuged at low speed. Virus from the aqueous phase was pelleted, resuspended in CsCl (ρ=l.33 g/cm3), density banded, pelleted and finally resuspended in 30 mM KCl and 6 mM Tris (pH 7.5) to a protein concentration of ˜3 mg/ml.


1985 ◽  
Vol 5 (7) ◽  
pp. 1787-1790
Author(s):  
I Deichaite ◽  
Z Laver-Rudich ◽  
D Dorsett ◽  
E Winocour

A linear simian virus 40 origin-containing DNA fragment replicated in monkey COS cells, generating tandemly repeated (head-to-tail) structures. Electron microscopy revealed circle-and-tail configurations characteristic of rolling-circle replication intermediates. Circularization of the same DNA before transfection led to a theta type of replication which generated supercoiled DNA molecules.


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