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dc.contributor.authorCollart, David G.
dc.contributor.authorStein, Gary S.
dc.contributor.authorStein, Janet L.
dc.date2022-08-11T08:10:56.000
dc.date.accessioned2022-08-23T17:25:48Z
dc.date.available2022-08-23T17:25:48Z
dc.date.issued1985-07-01
dc.date.submitted2011-01-14
dc.identifier.citationMol Cell Biochem. 1985 Jul;67(2):161-70.
dc.identifier.issn0300-8177 (Linking)
dc.identifier.pmid2931584
dc.identifier.urihttp://hdl.handle.net/20.500.14038/49487
dc.description.abstractRepetitive DNA sequences, derived from the human beta-globin gene cluster, were mapped within a series of human genomic DNA segments containing core (H2A, H2B, H3 and H4) and H1 histone genes. Cloned recombinant lambda CH4A phage with human histone gene inserts were analyzed by Southern blot analysis using the following 32P-labeled (nick translated) repetitive sequences as probes: Alu I, Kpn I and LTR-like. A cloned DNA designated RS002-5'C6 containing (i) a (TG)16 simple repeat, (ii) an (ATTTT)n repeat and (iii) a 52 base pair alternating purine and pyrimidine sequence was also used as a radiolabelled hybridization probe. Analysis of 12 recombinant phage, containing 6 arrangements of core histone genes, indicated the presence of Alu I, Kpn and RS002-5'C6 repetitive sequences. In contrast, analysis of 4 human genomic DNA segments, containing both core and H1 histone genes, indicated the presence of only Alu I family sequences. LTR-like sequences were not detected in association with any of the core or H1 histone genes examined. These results suggest that human histone and beta-globin genes share certain aspects of sequence organization in flanking regions despite marked differences in their overall structure and pattern of expression.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=2931584&dopt=Abstract">Link to Article in PubMed</a>
dc.relation.urlhttp://dx.doi.org/10.1007/BF02370175
dc.subjectBacteriophage lambda
dc.subjectChromosome Mapping
dc.subjectCloning, Molecular
dc.subjectDNA
dc.subjectGenes
dc.subjectGlobins
dc.subjectHistones
dc.subjectHumans
dc.subjectPlasmids
dc.subject*Repetitive Sequences, Nucleic Acid
dc.subjectSequence Homology, Nucleic Acid
dc.subjectCell Biology
dc.titleA series of repetitive DNA sequences are associated with human core and H1 histone genes
dc.typeJournal Article
dc.source.journaltitleMolecular and cellular biochemistry
dc.source.volume67
dc.source.issue2
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/stein/144
dc.identifier.contextkey1728449
html.description.abstract<p>Repetitive DNA sequences, derived from the human beta-globin gene cluster, were mapped within a series of human genomic DNA segments containing core (H2A, H2B, H3 and H4) and H1 histone genes. Cloned recombinant lambda CH4A phage with human histone gene inserts were analyzed by Southern blot analysis using the following 32P-labeled (nick translated) repetitive sequences as probes: Alu I, Kpn I and LTR-like. A cloned DNA designated RS002-5'C6 containing (i) a (TG)16 simple repeat, (ii) an (ATTTT)n repeat and (iii) a 52 base pair alternating purine and pyrimidine sequence was also used as a radiolabelled hybridization probe. Analysis of 12 recombinant phage, containing 6 arrangements of core histone genes, indicated the presence of Alu I, Kpn and RS002-5'C6 repetitive sequences. In contrast, analysis of 4 human genomic DNA segments, containing both core and H1 histone genes, indicated the presence of only Alu I family sequences. LTR-like sequences were not detected in association with any of the core or H1 histone genes examined. These results suggest that human histone and beta-globin genes share certain aspects of sequence organization in flanking regions despite marked differences in their overall structure and pattern of expression.</p>
dc.identifier.submissionpathstein/144
dc.contributor.departmentDepartment of Cell Biology
dc.source.pages161-70


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