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dc.contributor.authorStein, Gary S.
dc.contributor.authorBurtner, D. L.
dc.date2022-08-11T08:10:57.000
dc.date.accessioned2022-08-23T17:26:02Z
dc.date.available2022-08-23T17:26:02Z
dc.date.issued1975-04-16
dc.date.submitted2011-01-14
dc.identifier.citationBiochim Biophys Acta. 1975 Apr 16;390(1):56-68.
dc.identifier.issn0006-3002 (Linking)
dc.identifier.pmid1092368
dc.identifier.urihttp://hdl.handle.net/20.500.14038/49545
dc.description.abstractSerum stimulation of early as well as late passages of nondividing WI-38 human diploid fibroblasts to proliferate, results in DNA synthesis beginning at 12 hours and MITOSIS AT 20 HOURS. A 2-fold increase in the transcriptional activity of chromatin isolated from early and late passage W2-38 cells is evident one hour following serum stimulation. An increased synthesis and association with the genome of two defined molecular weight classes of nonhistone chromosomal proteins one hour following serum stimulation of early and late passage cells is also observed. The increased chromatin template activity and nonhistone chromosomal protein synthesis occur in early passage cells stimulated to proliferate in the presence of actinomycin D. However, when late passage WI-38 cells are stimulated in the presence of antinomycin D, increases in chromatin template activity and nonhistone chromosomal protein synthesis are not observed one hour following serum stimulation. The possibility that nonhistone chromosomal protein synthesis and activation of transcription early during the prereplicative phase of the cell cycle in early passage human diploid fibroblasts may be regulated at the translational level is discussed. Consideration is also given to the possibility that there may be an age-dependent modification in such a regulatory mechanism.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=1092368&dopt=Abstract">Link to Article in PubMed</a>
dc.relation.urlhttp://dx.doi.org/10.1016/0005-2787(75)90008-8
dc.subjectCell Division
dc.subjectCell Line
dc.subjectCell Nucleus
dc.subjectChromatin
dc.subjectChromosomes
dc.subjectDNA-Directed RNA Polymerases
dc.subjectDiploidy
dc.subjectDrug Stability
dc.subjectEscherichia coli
dc.subjectFibroblasts
dc.subject*Genes
dc.subjectHumans
dc.subjectLung
dc.subjectNucleoproteins
dc.subject*Protein Biosynthesis
dc.subjectRNA, Messenger
dc.subjectTemplates, Genetic
dc.subjectTime Factors
dc.subjectCell Biology
dc.titleGene activation in human diploid cells. Age-dependent modifications in the stability of messenger RNAs for nonhistone chromosomal proteins
dc.typeJournal Article
dc.source.journaltitleBiochimica et biophysica acta
dc.source.volume390
dc.source.issue1
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/stein/210
dc.identifier.contextkey1728517
html.description.abstract<p>Serum stimulation of early as well as late passages of nondividing WI-38 human diploid fibroblasts to proliferate, results in DNA synthesis beginning at 12 hours and MITOSIS AT 20 HOURS. A 2-fold increase in the transcriptional activity of chromatin isolated from early and late passage W2-38 cells is evident one hour following serum stimulation. An increased synthesis and association with the genome of two defined molecular weight classes of nonhistone chromosomal proteins one hour following serum stimulation of early and late passage cells is also observed. The increased chromatin template activity and nonhistone chromosomal protein synthesis occur in early passage cells stimulated to proliferate in the presence of actinomycin D. However, when late passage WI-38 cells are stimulated in the presence of antinomycin D, increases in chromatin template activity and nonhistone chromosomal protein synthesis are not observed one hour following serum stimulation. The possibility that nonhistone chromosomal protein synthesis and activation of transcription early during the prereplicative phase of the cell cycle in early passage human diploid fibroblasts may be regulated at the translational level is discussed. Consideration is also given to the possibility that there may be an age-dependent modification in such a regulatory mechanism.</p>
dc.identifier.submissionpathstein/210
dc.contributor.departmentDepartment of Cell Biology
dc.source.pages56-68


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