Nucleic Acids Research, 1984, Vol. 12, No. 6 2775-2790
© 1984
MOLECULAR BIOLOGY |
Structure and origin of a novel class of defective interfering particle of vesicular stomatitis virus
Department of Biology, University of California San Diego, La Jolla, CA 92093 *Department of Microbiology and Immunology, Washington University School of Medicine St. Louis, MO 63110, USA
Received December 12, 1983. Revised February 27, 1984. Accepted February 27, 1984.
The genome structure and terminal sequences of a ‘copyback’ defective interfering (DI) particle ST1, and a novel complexly rearranged ‘snapback’ DI particle ST2 of vesicular stomatitis virus have been determined. The ST1 DI genome RNA possesses 54 base long inverted complementary termini, the 5' end of which is homologous to the standard virus genome 5' end. Following this region of inverted complementarity the DI RNA 5' end continues to be homologous to standard virus RNA 5' sequences, whereas the 3' end diverges into sequences within the virus L gene internal sequences. ST2 DI genome RNA does not contain colinear covalently linked plus and minus sense RNA copies of the standard infectious virus RNA 5' terminus as predicted from the prototype snapback DI structure, but instead appears to be a hairpin copy of the ST1 DI RNA genome. This is the first evidence suggesting that DI particles may be generated from RNA templates other than the standard virus RNA. Generation models and the implications of these findings for RNA virus evolution are discussed