Electron microscopic and autoradiographic analysis of replicating DNA from Physarum showed that replication occurs at a rate of 0.4 micron/min/per replicon and that replicons of size 10--15 mu occur in temporal clusters with an average of about 4 replicons per cluster. These results are compared with previous hydrodynamic measurements and with those obtained in other organisms.
The direction of replication of DNA within replicons of Physarum polycephalum was studied by pulse-labelling with 5-bromouracil-deoxyriboside (BrdUrd) and 3H-adenosine deoxyriboside (dAdo), followed by ultraviolet- (UV) -photolysis and analysis of molecular weights of single strand DNA fragments on alkaline sucrose gradients. Newly made DNA within replicons at all stages of completion is split in two equal halves upon UV irradiation when BrdUrd was given at the time of initiation of DNA synthesis. This shows that replication within replicons of Physarum polycephalum starts at an origin located in the center of each unit, proceeding bidirectionally from this origin.
Combinations of 5-bromodeoxyuridine (BrdUrd) and 3H-deoxyadenosine (3H-DAdo) short pulses were given in the synchronous DNA-replication period of Physarum polycephalum. After a chase period, UV-photolysis products were analyzed on alkaline sucrose gradients. This strategy has allowed the following conclusions. a) at the time of master-initiation of DNA replication, points separated by 1.1-2.2x10(7) daltons of single strand DNA may initiate DNA synthesis. b) among these, only selected groups of replicons actually proceed in DNA replication at this time, while others appear to hold (later temporal sets of replicons). The origins of the ones that proceed in replication are separated from each other by a distance corresponding to 1.1-2.x10(7) daltons. c) regions in actual replication are separated from each other by increasing distances (up to 1.5x10(8) daltons single strand DNA) at later times in S.
DNA from synchronously replicating nuclei of Physarum polycephalum was studied electron microscopically after 15, 30, 60, and 90 or 120 min of replication in the presence or absence of the protein synthesis inhibitor cycloheximide. The replication-loop size-distribution showed that replication fork progression is severely retarded in the presence of cycloheximide. Analysis of replication-loop frequency showed a similar pattern in control and cyclo-heximidetreated samples, with an increase from 15 to 30 and 60 min. This suggests, surprisingly, that initiations of new replicons either may not be inhibited by cycloheximide or, alternatively, that all initiations have already taken place at the very start of S-phase. The latter conclusion is favored in the light of previous results in our laboratory, discussed here.We have previously suggested that the genome of Physarum polycephalum replicates as sets of replicons of size around 2-4 X 107 daltons (5-10 gm), occurring in temporal clusters of 3-4 (1). This model, arrived at by analysis of alkaline sucrose sedimentation patterns, was verified by electron microscope and autoradiographic analysis of replicating DNA (2). An earlier study on the effects of inhibition of protein synthesis with cycloheximide during S-phase suggested the following model for control of DNA-replication in Physarum (3): at least 10 temporal sets of replication units depend for their consecutive initiations on ongoing protein synthesis, while replicons once initiated are no longer protein-synthesis dependent. Evans et al. (5) concluded, however, that cycloheximide did not interfere with initiation of new replication units, while elongation of initiated progeny strands was inhibited. In our previous study on the effects of inhibition of protein synthesis on DNA replication (4), we found that the chain length increase of new DNA strands was slowed or prevented at three levels: (a) formation of Okazaki fragments, (b)joining of Okazaki fragments to replicon size DNA, and (c) maturation (joining) of replicon size DNA to high molecular weight DNA.It is possible that the latter two effects could be a consequence of the first. This result, as well as that of Evans et al. In this communication we have analyzed DNA-replication in the presence and absence of the protein synthesis inhibitor, cycloheximide, using electron microscopy. The main purpose of this study was to shed light on the question of whether fork progression (replication rate) is unaffected or slowed or stopped in the presence of cycloheximide. We also hoped to be able to reveal whether new initiations can occur in the absence of protein synthesis.
MATERIALS AND METHODS
Strains and Culture MethodsPlasmodial strain TU291 was also used in all our previous studies on DNA replication in Physarum polycephalunt This strain is very closely related to the cycloheximide-resistant strain which we have used to demonstrate that the effects ofcycloheximide on DNA replication are mediated exclusively through the effect on protein synthesis (4). T...
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