1980
DOI: 10.1016/0014-5793(80)80185-2
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Methylation of DNA in L cells on replication

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Cited by 19 publications
(6 citation statements)
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“…Unlike methylation of ligated DNA products, methylation of Okazaki fragments was relatively resistant to various inhibitors of the methylation reaction (S isobutyladenosine and others) and it was not inhibited by hormones (auxins in plants). We concluded that the nucleus should contain a few DNA methyltrans ferases, each of them serving at a particular replication stage and differing from others in site specificity and sen sitivity to respective inhibitors [69,74]. This is now in a full agreement with modern data on the multiplicity of DNA methyltransferases in plant and animal cell.…”
supporting
confidence: 63%
“…Unlike methylation of ligated DNA products, methylation of Okazaki fragments was relatively resistant to various inhibitors of the methylation reaction (S isobutyladenosine and others) and it was not inhibited by hormones (auxins in plants). We concluded that the nucleus should contain a few DNA methyltrans ferases, each of them serving at a particular replication stage and differing from others in site specificity and sen sitivity to respective inhibitors [69,74]. This is now in a full agreement with modern data on the multiplicity of DNA methyltransferases in plant and animal cell.…”
supporting
confidence: 63%
“…[40][41][42][43] To assess when during the cell-cycle DNA methylation in PMDs and HMDs is maintained, we measured DNA methylation using a novel reduced representation method in human p51R mesenchymal cells (supplemental Figure 7), which are highly responsive to serum starvation-induced cell-cycle block. 44 Comparison of p51R cells that were cycling or blocked for 96 hours in G0/G1 by serum starvation ( Figure 7F) revealed that the genome of G0/G1-arrested cells was more methylated than that of cycling cells (P , .001, Wilcoxon rank sum test; Figure 7G) and exhibited fewer PMDs ( Figure 7H), covering 55.5% of the genome compared with 58% in cycling cells.…”
Section: Change Of Chromatin Structure During Erythroid Differentiatimentioning
confidence: 99%
“…This enzymatic DNA modification in bacteria is an essential element of the host modification and restriction systems and it is involved often in the regulation of replication and transcription. m 6 A was also found in DNA of eukaryotes such as protozoa [2–7], slime molds [8], fungi [9], algae [10] and higher plants [11]. While the attempts to isolate this base from different animal DNA were unsuccessful [12] there is some indirect evidence of the possible presence of m 6 A in mammalian DNA [13,14].…”
Section: Introductionmentioning
confidence: 99%