Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: EC:2.7.7.7 (DNA polymerase)
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Amoeba discoides nuclear protein partially purified by passage through Sephadex G-200 showed 3 high-mol.-wt. DNA polymerase activities which eluted in and just following the void volume. No low-mol.-wt (45,000 daltons) DNA polymerase beta activity was detected. Nuclear protein layered on 5--20% sucrose gradients also showed an absence of low-mol.-wt DNA polymerase beta. The void volume enzyme showed deoxyribonuclease activity, but no low-mol.-wt nuclease activity was detected.
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PMID:Absence of low molecular weight DNA polymerase activity from the nuclei of Amoeba discoides. 63 29

Nuclear protein factor type 1 (NPF-1) that simulates IMR-32 primase-associated DNA polymerase alpha 1 and alpha 2 activities has been purified from a high-salt extract of liver chromatin from 6-month-old rats. The final purified factor lacks DNA polymerase alpha, RNA polymerase, and DNA-unwinding or topoisomerase type I activities. The stimulatory activity is destroyed by trypsin (60 min at 37 degrees C), DNase II (60 min at 37 degrees C), and heat treatment (2 min at 68 degrees C). The 125I-labeled NPF-1 does not bind to activated calf thymus DNA or poly(dC). However, it forms a ternary complex with DNA in the presence of DNA polymerase alpha-primase complex (alpha 1 and alpha 2). The ternary complex sediments on sucrose density gradient as a heavier band (11S). The NPF-1 also stimulates (2.5-fold) primase-catalyzed incorporation of GMP and dGMP from the corresponding triphosphates on poly(dC) template even in the presence of a high concentration of alpha-amanitin (400 micrograms/ml). The labeled duplex containing the poly(dC) template, [32P]-GTP, and [3H]dGTP loses 80% of the 32P label and 70% of the 3H label after treatment with 0.3 M KOH and DNase I, respectively. The products were isolated from reaction mixtures incubated with and without NPF-1 and subjected to alkaline sucrose-density-gradient sedimentation analysis. The results suggest that the rate of synthesis of DNA short chains is increased in the presence of NPF-1 without a concomitant increase in the chain length of the newly synthesized products.
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PMID:Stimulation of human neuroblastoma DNA polymerase alpha and primase activities by a protein factor isolated from rat liver chromatin. 354 Sep 37

Studies have shown that certain strain-specific characters of large, free-living amoebae may be influenced by the microinjection of non-homologous low molecular weight RNAs. To investigate the mechanisms involved in 'information' transfer, the template preferences of partially purified DNA polymerase activities isolated from Amoeba discoides have been studied. After passage through Sephadex G-200, DNA polymerase activities from whole homogenates could utilize both 'activated' calf thymus DNA and the synthetic ribohomopolymer poly rA oligo d(pT)10 as templates. Fractionation using different saturations of (NH4)2SO4 showed that there was no detectable poly A d(pT)10-directed DNA polymerase activity in the extra-mitochondrial cytoplasm, and the ability to utilize this template appeared to be located in the nuclei. Nuclear protein passed through short (30 cm) columns of Sephadex G-200 showed DNA polymerase activities which could use both synthetic and natural RNA as templates, but little activity was detected when using longer (70 cm) columns, although DNA-directed DNA polymerase activities were more clearly defined. Use of DEAE-cellulose only revealed a low (1--3%) activity with poly A d(pT)10 compared to the activity observed using 'activated' calf thymus DNS. DNA polymerase activities of amoebae showed a response to added RNA templates which depended on the purity of the enzyme preparation, and the possibility that these enzymes are involved in 'information' transfer cannot be ruled out.
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PMID:Informational molecules in amoebae studies of template utilization by the DNA polymerase activities of Amoeba discoides. 615 39

An increase was observed in the total protein mass of nuclei isolated from Chinese hamster ovary cells heated at 45 degrees C or 45.5 degrees C. An increase in the fractional recovery of DNA polymerase alpha and beta, and of DNA topoisomerase activity coincided with this increase in the protein mass of nuclei from heated cells. Nuclear protein mass which was soluble in 2.0 M NaCl decreased 0.5 fold, while DNA-associated and nuclear matrix-associated protein mass increased 2.2 and 3.4 fold, respectively. The results indicate that the increase in nuclear protein mass observed in nuclei from heated cells is due in part to an increased binding, or precipitation, of nuclear proteins onto the cell's DNA and nuclear matrix.
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PMID:Nuclear protein redistribution in heat-shocked cells. 838 Nov 27