TY - JOUR
T1 - Deletion mapping of sindbis virus DI RNAs derived from cDNAs defines the sequences essential for replication and packaging
AU - Levis, Robin
AU - Weiss, Barbara G.
AU - Tsiang, Manuel
AU - Huang, Henry
AU - Schlesinger, Sondra
N1 - Funding Information:
We thank Sherry Gee, David Kingsbury II, and Dr. Richard Rosenthal for their excellent technical assistance. We thank Wayne Barnes for providing advice, Ml3 bacteriophage, and bacterial strains, and Thomas Kunkel for providing bacterial strains. This work was supported by grants from the National Institute of Allergy and Infectious Diseases, the American Cancer Society, and the Monsanto/Washington University Biomedical Research Contract. R. L. has been supported by a Cellular and Molecular Biology Training Grant from the National Institutes of Health. She is currently a Stephen Morse Fellow in Microbiology and Immunology.
PY - 1986/1/17
Y1 - 1986/1/17
N2 - Defective-interfering (DI) genomes of a virus contain sequence information essential for their replication and packaging. They need not contain any coding information and therefore are a valuable tool for identifying cis-acting, regulatory sequences in a viral genome. To identify these sequences in a DI genome of Sindbis virus, we cloned a cDNA copy of a complete DI genome directly downstream of the promoter for the SP6 bacteriophage DNA dependent RNA polymerase. The cDNA was transcribed into RNA, which was transfected into chicken embryo fibroblasts in the presence of helper Sindbis virus. After one to two passages the DI RNA became the major viral RNA species in infected cells. Data from a series of deletions covering the entire DI genome show that only sequences in the 162 nucleotide region at the 5′ terminus and in the 19 nucleotide region at the 3′ terminus are specifically required for replication and packaging of these genomes.
AB - Defective-interfering (DI) genomes of a virus contain sequence information essential for their replication and packaging. They need not contain any coding information and therefore are a valuable tool for identifying cis-acting, regulatory sequences in a viral genome. To identify these sequences in a DI genome of Sindbis virus, we cloned a cDNA copy of a complete DI genome directly downstream of the promoter for the SP6 bacteriophage DNA dependent RNA polymerase. The cDNA was transcribed into RNA, which was transfected into chicken embryo fibroblasts in the presence of helper Sindbis virus. After one to two passages the DI RNA became the major viral RNA species in infected cells. Data from a series of deletions covering the entire DI genome show that only sequences in the 162 nucleotide region at the 5′ terminus and in the 19 nucleotide region at the 3′ terminus are specifically required for replication and packaging of these genomes.
UR - http://www.scopus.com/inward/record.url?scp=0022498060&partnerID=8YFLogxK
U2 - 10.1016/0092-8674(86)90492-7
DO - 10.1016/0092-8674(86)90492-7
M3 - Article
C2 - 3753584
AN - SCOPUS:0022498060
SN - 0092-8674
VL - 44
SP - 137
EP - 145
JO - Cell
JF - Cell
IS - 1
ER -