CaltechAUTHORS
  A Caltech Library Service

High-molecular-weight RNAs of AKR, NZB, and wild mouse viruses and avian reticuloendotheliosis virus all have similar dimer structures

Bender, Welcome and Chien, Yueh-Hsiu and Chattopadhyay, Sisir and Vogt, Peter K. and Gardner, Murray B. and Davidson, Norman (1978) High-molecular-weight RNAs of AKR, NZB, and wild mouse viruses and avian reticuloendotheliosis virus all have similar dimer structures. Journal of Virology, 25 (3). pp. 888-896. ISSN 0022-538X. http://resolver.caltech.edu/CaltechAUTHORS:BENjvir78

[img]
Preview
PDF
See Usage Policy.

2343Kb

Use this Persistent URL to link to this item: http://resolver.caltech.edu/CaltechAUTHORS:BENjvir78

Abstract

Several 50 to 70S tumor viral RNAs have previously been shown by electron microscopy to be dimers, with the two monomer subunits joined near their 5' ends. Five additional naturally occurring type C RNA tumor viruses have now been examined: AKR, and endogenous murine ecotropic virus; NZB, an endogenous murine xenotropic virus; and ecotropic and an amphotropic virus isolated from a wild mouse; and the avian reticuloendotheliosis virus (REV). All five 50 to 70S RNAs have similar 5'-to-5' dimer structures. Therefore, the observations support the hypothesis that the dimer linkage is a structural feature common to all type C mammalian viruses. REV is the first example of an avian virus with a clear 5'-to-5' dimer linkage. All of the mammalian viral RNAs, but not REV, showed symmetrically placed loops in each subunit of the dimer. Possible molecular structures and biological functions of the dimer linkages and loops are discussed.


Item Type:Article
Additional Information:Copyright © 1978, American Society for Microbiology. Received for publication 20 October 1977 We thank Marilyn R. Lander and Wallace P. Rowe of the National Institute of Allergy and Infectious Diseases for assistance and advice. W.B. has been the recipient of a National Science Foundation fellowship and of a Public Health Service training grant from the National Institute of General Medical Sciences. This research has been supported by Public Health Service contracts NO1-CP-43306 and NO1-CP-53500 with the Virus Cancer Program of the National Cancer Institute. Y.C. has been supported by Public Health Service postdoctoral fellowship no. 5-F32-CA-05099 from the National Cancer Institute.
Record Number:CaltechAUTHORS:BENjvir78
Persistent URL:http://resolver.caltech.edu/CaltechAUTHORS:BENjvir78
Alternative URL:http://pubmedcentral.gov/articlerender.fcgi?artid=525983
Usage Policy:No commercial reproduction, distribution, display or performance rights in this work are provided.
ID Code:2232
Collection:CaltechAUTHORS
Deposited By: Archive Administrator
Deposited On:17 Mar 2006
Last Modified:26 Dec 2012 08:48

Repository Staff Only: item control page