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Biomedical subjects

R B Inman

Publications and source records attributed to R B Inman.

At least 55 records · Page 3Linked to original sources

Electron microscopic identification of supercoiled regions in complex DNA structures.

When intracellular lambda replicative intermediates (theta structures) are intercalated with psoralen and then irradiated with long wavelength ultraviolet light (u.v.), interstrand crosslinks are produced. After purification and denaturation of these theta structures, a global difference in denaturation can be observed by electron microscopy; parental sections are essentially native whereas daughter segments are highly denatured. This difference can be explained if parental sections are covalently continuous (and therefore able to supercoil) and daughter segments are not. Due to the higher thermal stability of supercoiled DNA, parental DNA will remain native while daughter sections will denature. Because these structures are crosslinked, the thermal treatment does not lead to dissociation of the highly denatured daughter strands. Experiments with simple negatively supercoiled plasmid circles support the above conclusions. When circles are crosslinked with psoralen-u.v. and then denatured, they remain native because of the higher thermal stability of covalently closed structures. If the circles are linearized before heating but after the psoralen-u.v. treatment, the thermal stability effect is eliminated and the molecules become highly denatured. In this case, however, the crosslinking density is found to be higher than in samples linearized before psoralen-u.v. treatment. This, therefore, shows that crosslinking density also reflects the superhelical state of the molecule at the time of psoralen-u.v. treatment. Two different properties can be used to discriminate between supercoiled and covalently discontinuous domains in complex DNA structures. First, supercoiled regions remain native while covalently discontinuous segments denature following a thermal treatment. This effect requires that covalent continuity exists up to and during the heating treatment. Second, because negative superhelicity enhances psoralen intercalation, crosslinking density is higher in these regions. Even if supercoiled domains are destroyed after the psoralen-u.v. treatment, the imprint of superhelicity is retained and can be recognized as a higher than normal crosslinking density.

Bacteriophage lambda↗

Reinitiation at the lambda DNA origin accompanies the host SOS response.

Abnormal reinitiation of replication from lambda origins has previously been found during infection in the presence of caffeine or cis-diamminedichloroplatinum II (cis-Pt) or when lambda infects a P2 lysogen. It was further shown that the reinitiations arising from cis-Pt treatment took place during the SOS response induced by the template damage caused by the drug. It is now shown that SOS induction by uv irradiation of the host also results in reinitiation events and that it is the SOS response itself rather than some other direct effect of the damaged host template that is responsible for the phenomenon. Parental sections of lambda replicative intermediates can supercoil, whereas daughter segments cannot. To explain the control that prevents reinitiation, it is proposed that normally the origin sequence has to be under superhelical tension to be a suitable substrate for the initiating machinery; once a round is in progress, the daughter origin sequences would not be under such tension and would therefore be inactive. It is shown that in an SOS environment the proposed requirement for a superhelical origin sequence is relaxed and consequently the control against reinitiation lost. Under such conditions, primary growing points that have encountered template lesions terminate and a new wave of replication initiates.

Bacterial Proteins↗

Multiply branched DNA molecules from bacteriophage lambda: putative post-replicational repair DNA intermediates.

Previous studies have shown that thymidine deprivation causes the formation of multiply branched molecules among bacteriophage lambda DNA replicative intermediates. In the present report, we present supporting evidence indicating that the induction of the SOS response is involved in this process. Moreover, close inspection of the DNA replicatives intermediates present in a recA deficient strain, shows an accumulation of gapped replicative intermediates. From these observations we postulate a model by which multiply branched DNA molecules may be intermediates or derived intermediates of a post-replicational repair pathway.

Bacteriophage lambda↗

An immobilized fork as a termination of replication intermediate in Bacillus subtilis.

The structure of a DNA intermediate associated with termination of chromosome replication in Bacillus subtilis and derived from a unique BamHI 24.8 X 10(3) base-pair (bp) region of the chromosome has been investigated. The intermediate has properties expected for a forked structure. Gel electrophoresis followed by Southern transfer and hybridization to cloned DNA has shown it to comprise single strands of 15.4 X 10(3) bp and 24.8 X 10(3) bp, in approximately equimolar amounts. After purification away from the bulk of chromosomal DNA, electron microscopy of the intermediate established that 15% of the DNA was present as branched molecules and a significant proportion (11 of 31) of these contained two arms of matching length. The average dimensions (best estimates) of this unique class of Y-shaped molecule were 9.5(+/- 0.3) X 10(3), 15.1(+/- 0.4) X 10(3) and 24.6 24.6(+/- 0.6) X 10(3) bp for the stem, arms and end-to-end length, respectively. These values are consistent with the single strand composition of the intermediate as found. Furthermore, hybridization of the single strands to DNA from known locations within the BamHI 24.8 X 10(3) bp region has established the orientation of the forked intermediate relative to the genetic map. The intermediate presumably reflects the immobilization of the clockwise replication fork within the 24.8 X 10(3) bp region, at a location approximately 15.4 X 10(3) bp from the right end.

Bacillus subtilis↗

Bacteriophage P4 DNA replication. Location of the P4 origin.

An electron microscopic examination of replicating bacteriophage P4 DNA molecules has revealed theta-type structures that replicate bidirectionally from a single origin. Many replicating P4 DNA molecules also contain long (2000 bases) single-strand DNA regions at the growing fork that are deployed in a trans configuration, which supports the concept of continuous leading strand and discontinuous lagging strand syntheses. The position of the P4 origin was localized by the use of a plasmid complementation test for replication in vivo, as well as by labeling of DNA replicating in vitro in the presence of a chain-terminating inhibitor. During this study we discovered a second site on the P4 genome which is essential for replication, and we have named it crr (cis region required for replication). The site is located at least 3300 bases from the origin but appears to be required for the initiation of DNA replication in vivo as well as in vitro.

Coliphages↗

Reinitiation during lambda DNA replication resulting from either cis-Pt treatment or infection of a P2 lysogenic strain.

Nested areas of replication are observed in phage lambda replicative intermediates and arise from reinitiation from the lambda origin. Reinitiation occurs when the first round of lambda replication takes place in the presence of the drug cis-Pt or when lambda infects a host which has been preincubated with the drug. In the latter case it is shown that the infection proceeds during the expression of SOS functions induced in the host as a result of the drug treatment. When lambda infects a host lysogenic for phage P2, an interference process occurs which prevents formation of lambda phage. The lambda DNA does, however, undergo at least one round of replication but is abnormal in that lambda origins reinitiate to form nested areas of replication similar to those resulting from exposure to the drug cis-Pt.

Bacteriophage lambda↗

Methodology for the study of the effect of drugs on development and DNA replication in Drosophila melanogaster embryonic tissue.

Methodology is described that will permit the study of the effect of various drugs on development and DNA replication in the cleavage nuclei of Drosophila eggs. It is shown that permeabilized eggs can be exposed to an aqueous incubation medium for up to 30 min without measureable effects on development and that such incubations can be performed with eggs that have a relatively sharp age distribution. The effect on development and viability of a variety of drugs has been examined as an aid for future studies directed toward achieving synchronous development in a population of eggs and electron microscopic studies of DNA replication in the presence of various drugs.

Animals↗

The role of gene O protein in the replication of bacteriophage lambda.

The role of the product of gene O of bacteriophage lambda in phage DNA replication was examined by shifting cells infected with an Ots mutant to the nonpermissive temperature after incubation at the permissive temperature. Thymidine incorporation after the temperature shift exhibits biphasic kinetics, with rapid synthesis immediately after the shift and slower synthesis 2-15 min after the shift. Following a shift to the nonpermissive temperature early in infection, the proportion of replicative intermediates decreases substantially and sigma-structures are favored for preservation. When the shift is done late in infection, the proportion of replicative intermediates remains the same. The average length of single-stranded regions at the branch points increases after a shift to the nonpermissive temperature. Most of the counts which are incorporated after the temperature shift are incorporated into strands which are longer than unit length. These results favor a model in which lambda O protein is required for the initiation of replication, but at least some elongation can continue in the absence of O. It is possible that O protein plays a role in elongation of the lagging strand at replicative forks. This model suggests a way to regulate the transition between theta and sigma replication which occurs as lambda infection proceeds.

Bacteriophage lambda↗

Bacteriophage P2 DNA replication. Characterization of the requirement of the gene B protein in vivo.

Replicative intermediates isolated from Escherichia coli cells infected with P2 gene B mutants were circular DNA molecules with single-stranded DNA tails, as opposed to the double-stranded DNA tails of wild-type replicative intermediates. The results show that the mutant replicative intermediates arose from aberrant DNA replication, aberrant due to a lack of lagging strand DNA synthesis, but with normal leading strand synthesis, so that only one circular duplex daughter DNA molecule was made from each duplex parent molecule. The single-stranded tails were shown to correspond to the nicked (and therefore displaced) parental DNA "l" strands. By partial denaturation mapping, the ends of the single-stranded tails tended to map close to the replication origin, but not all at a unique position, probably due to partial degradation or breakage in vivo, or during cell lysis or DNA isolation. By hybridization to separated strands of P2 DNA on nitrocellulose filters, DNA synthesis was shown to be asymmetric, and consistent with more leading strand than lagging strand synthesis having occurred. We concluded that the gene B protein is required for lagging strand DNA synthesis, but not for initiation, elongation or termination of the leading strand.

Centrifugation, Density Gradient↗

Physical evidence for the temporal transition of transcription in bacteriophage lambda.

A high proportion of intracellular lambda DNA molecules are found to have D-loops, when isolated under four different conditions: (1) lambda Ots after 7 min at 31 degrees C in the presence of chloramphenicol; (2) lambda Ots after 7 min at 31 degrees C without chloramphenicol; (3) lambda Ots after 30 min at 42 degrees C; and (4) lambda cIIcIII after 50 min at 37 degrees C. The great majority of these D-loops contain RNA and are produced by E. coli RNA polymerase. In the presence of chloramphenicol, D-loops are mostly limited to the immediate early regions of the major leftward and rightward operons. At early times, with no chloramphenicol present, D-loops map primarily within the delayed early regions of the two major operons. At late times, D-loops are found mostly within the major late operon of the bacteriophage DNA. This physical evidence corroborates evidence of the temporal transition in lambda transcription obtained by other means. Chloramphenicol is shown to block the transition from immediate early to delayed early transcription.

Bacteriophage lambda↗

Direction of bacteriophage lambda DNA replication in a thymine requiring Escherichia coli K-12 strain. Effect of thymidine concentration.

The direction of replication was established for the first round of bacteriophage lambda DNA replication in thymine requiring E. coli K-12 cells exposed to different concentrations of thymidine. It was found that a dramatic decrease in the proportion of bidirectionally replicating molecules followed a decrease in the concentration of thymidine. Moreover, the rightward mode of replication appears to be exclusively favored in unidirectionally replicating molecules found at low concentrations of thymidine.

Bacteriophage lambda↗

Isolation of DNA fragments containing replicating growing forks from both E. coli and B. subtilis.

By the use of a restriction enzyme digestion of gently lysed E. coli or B. subtilis cells, it is possible to isolate a minute fraction of the total DNA that has an unusually high sedimentation coefficient. Upon inspection of this DNA in the electron microscope, branched DNA fragments are observed. Single branched DNA fragments were analyzed by restriction enzyme and partial denaturation mapping techniques. The fragments appear to have the properties of growing forks excised from in vivo replicating intermediates. In B. subtilis, the minute fraction of DNA was also investigated by transformation assays and found to be greatly enriched for a marker near the origin and slightly enriched for a terminus marker.

Bacillus subtilis↗

Multiply branched replicative intermediates in E. coli and bacteriophage lambda.

Multiple branched DNA fragments present in a fast sedimenting complex comprising a minute fraction of the E. coli genome have been isolated. Similar structures were also observed among bacteriophage lambda DNA replicative intermediates after infection of synchronized E. coli cells. These structures were found to be associated with the amino acid and thymidine starvation steps required for synchronization and originate either by initiation from secondary sites or by snap-back of daughter strands containing substantial single stranded regions in the vicinity of the growing point.

Bacteriophage lambda↗