Structural properties of double-stranded RNAs associated with biological control of chestnut blight fungus.

Printer-friendly versionPrinter-friendly versionPDF versionPDF version
TitleStructural properties of double-stranded RNAs associated with biological control of chestnut blight fungus.
Publication TypeJournal Article
Year of Publication1986
AuthorsTartaglia, J, Paul, CP, Fulbright, DW, Nuss, DL
JournalProc Natl Acad Sci U S A
Volume83
Issue23
Pagination9109-13
Date Published1986 Dec
ISSN0027-8424
Abstract

Double-stranded RNAs (ds RNAs) are thought to be the cytoplasmic determinants responsible for the phenomenon of transmissible hypovirulence in the chestnut blight fungus Endothia parasitica [Murr.] Anderson. The three major ds RNA components associated with the North American hypovirulent strain, Grand Haven 2, were characterized with respect to molecular-hybridization specificity and RNase T1-digestion patterns. The large (L-RNA; approximately 9 kilobase pairs) and middle-sized (M-RNA; approximately 3.5 kilobase pairs) ds RNA components cross-hybridized under stringent conditions and exhibited indistinguishable partial and complete RNase T1 digestion patterns relative to their 5' and 3' termini. These results suggest that M-RNA was derived from L-RNA by an internal deletion event. The small (S-RNA; approximately 1 kilobase pair) RNA was unrelated to L- and M-RNA by these criteria. However, all three ds RNA components contained RNase T1-resistant oligonucleotides at one 5' terminus and at the corresponding 3' terminus of the complementary strand. These RNase T1-resistant species exhibited properties consistent with stretches of poly(uridylic acid) and poly(adenylic acid), respectively. The combined results are discussed in terms of the structural organization of hypovirulence-associated ds RNA molecules and their similarities to "double-stranded" RNA molecules observed in plant and animal cells infected with single-stranded RNA viruses.

Alternate JournalProc. Natl. Acad. Sci. U.S.A.
PubMed ID16593785
PubMed Central IDPMC387084