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J Gen Virol 56 (1981), 141-151; DOI 10.1099/0022-1317-56-1-141
© 1981 Society for General Microbiology

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Transfer RNAs Associated with Vesicular Stomatitis Virus

Cheryl L. Isaac and Jack D. Keene

Department of Microbiology and Immunology, Duke University Medical Center, Durham, North Carolina 27710, U.S.A.

The predominant RNAs in purified VSV particles are 42S and 4S in size. The 4S RNA is host transfer RNA that did not incorporate detectable radiolabel during VSV infection and was detected by in vitro labelling. Surprisingly, when BHK cells were prelabelled for 30 to 54 h before infection, the incorporation of [3H]uridine and [32P]orthophosphate into virus tRNAs remained very low and virus tRNAs were found to have a 5- to 15-fold lower specific activity than the total host tRNA, the value depending, in part, upon the period of prelabelling. Two-dimensional gel electrophoresis and partial sequence analysis indicated that the virus tRNAs include most species of host tRNA and no singly predominant species was apparent. Transfer RNAs are packaged by several enveloped viruses, but we have not found 4S RNA in reovirus, which lacks an envelope. We suggest that VSV contains a membrane-associated population of tRNA which has a slower rate of turnover than the total population of cellular tRNA.

Keywords: transfer RNA, VSV, radiolabelling, electrophoresis

Received 4 February 1981; accepted 15 May 1981.





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Copyright © 1981 by the Society for General Microbiology.