Transcription and translation in the autonomous parvovirus KRV.

We describe here the isolation and partial characterization of at least five viral specific RNAs synthesized in the rat nephroma (RN) cell after infection with the parvovirus KRV. The RNAs have the approximate lengths of 4.7, 3.4, 3.0, 1.25, and 0.95 kilobases (kb) and are probably the functional messages. The 4.7-kb RNA would represent a transcript of 95 to 100% of the viral genome. The most abundant message, about 3.0 kb, represents over 50% of the viral genome and probably codes in the reticulocyte transcribing system for the most abundant viral protein (MW 68,000) which is the main viral capsid protein. This abundant RNA, on the basis of R loop data, has an origin of transcription about 0.38 to 0.42 map units from the 3' end of the single-stranded KRV genome.

Synthesis of mRNA by the parvovirus KRV in isolated nuclei.

We have synthesized vial-specific transcripts in nuclei isolated from cells infected with the parvovirus Kilham rat virus. Radioactive vial-specific RNA synthesized in the nuclei was extracted, hybridized to viral DNA, incubated in glyoxal, and electrophoresed in an agarose gel. At least five viral-specific RNAs were detected containing 4.6 Kb (25-26S), 3.2 Kb (major species, 20-22S), 2.9 Kb, 1.3 Kb, and 1.0 Kb pairs. The 4.6 Kb RNA represents a transcript of 95-100% of the viral genome. The major 3.2 and 2.9 Kb RNAs represent a transcript of 50-60% of the viral genome. Over 65% of the viral-specific RNA in the isolated nuclei is polyadenylylated on the 3' terminus. The 5' terminus of the RNA is capped in vitro by the sequence m7G(5')ppp(5')A. Incorporation of [beta-32p]ATP into the 5' cap sequence suggests that initiation of viral RNA synthesis may occur in the infected isolated nuclei.

Timing of swarmer cell cycle morphogenesis and macromolecular synthesis by Hyphomicrobium neptunium in synchronous culture.

The swarmer cycle of Hyphomicrobium neptunium consists of a temporal sequence of discrete developmental events. To time morphogenesis and to investigate modulations in macromolecular synthesis, we attempted methods for synchronous culture. During synchrony, swarmer maturation occurred over 32%, hyphal growth occurred over 36%, and bud maturation occurred over 32% of the time required to complete the swarmer cycle. Daughter cells were released after 265 min. Deoxyribonucleic acid replication was discontinuous, having a G1 period of approximately 180 min. In addition, ribonucleic acid and protein syntheses were depressed during the earlier phases of development.

In vitro synthesis of double-stranded DNA from the Kilham rat virus single-stranded DNA genome.

Double-stranded, full-length linear DNA was synthesized in vitro by using single-stranded linear DNA as a self-priming template from the parvovirus Kilham rat virus and Escherichia coli DNA polymerase "large fragment" as the polymerizing enzyme. To ascertain the order of the synthesis of the cleavage fragments and to assess the accuracy of the in vitro synthesis, restriction endonuclease cleavage sites with known recognition sequences were mapped on the DNA. Comparing the cleavage pattern of the synthesized DNA with that of double-stranded viral DNA isolated from infected cells confirms that the in vitro synthesis produces a faithful copy of the viral single-stranded genome. Electron micrographs of the in vitro product reveal it to be a double-stranded linear molecule.