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dc.contributor.authorDworetzky, Steven I.
dc.contributor.authorWright, Kenneth Lynn
dc.contributor.authorFey, Edward G.
dc.contributor.authorPenman, Sheldon
dc.contributor.authorLian, Jane B.
dc.contributor.authorStein, Janet L.
dc.contributor.authorStein, Gary S.
dc.date2022-08-11T08:08:57.000
dc.date.accessioned2022-08-23T16:13:38Z
dc.date.available2022-08-23T16:13:38Z
dc.date.issued1992-05-01
dc.date.submitted2008-09-04
dc.identifier.citation<p>Proc Natl Acad Sci U S A. 1992 May 1;89(9):4178-82.</p>
dc.identifier.issn0027-8424 (Print)
dc.identifier.doi10.1073/pnas.89.9.4178
dc.identifier.pmid1570345
dc.identifier.urihttp://hdl.handle.net/20.500.14038/33671
dc.description.abstractWe have identified a nuclear matrix-attachment region within an upstream element of a human H4 histone gene promoter. Nuclear matrix proteins, isolated and solubilized from HeLa S3 cells, were found to interact with sequence specificity at this matrix-attachment region. Several types of assays for protein-DNA interaction showed that the minimal sequence for the nuclear matrix protein-DNA interaction was 5'-TGACGTCCATG-3'; the underlined region corresponds to the core consensus sequence for ATF transcription factor binding. Two proteins with molecular masses of 43 and 54 kDa were identified by UV-crosslinking analysis as integral components of this protein-DNA complex. The molecular masses of these proteins and the ATF-binding site consensus sequence suggest that these proteins are members of the ATF family. Our results provide direct evidence for nuclear matrix localization of sequence-specific DNA-binding factors for an actively transcribed gene. The proximity of a strong positive transcriptional regulatory element to the matrix-attachment region of this gene suggests that the nuclear matrix may serve to localize and concentrate trans-acting factors that facilitate regulation of gene expression.
dc.language.isoen_US
dc.relation<p><a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=1570345&dopt=Abstract">Link to article in PubMed</a></p>
dc.relation.urlhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC525656/
dc.subjectBase Sequence; Binding Sites; Consensus Sequence; Cross-Linking Reagents; DNA-Binding Proteins; Hela Cells; Histones; Humans; Molecular Sequence Data; Molecular Weight; Nuclear Matrix; Nuclear Proteins; Promoter Regions (Genetics); Restriction Mapping
dc.subjectLife Sciences
dc.subjectMedicine and Health Sciences
dc.titleSequence-specific DNA-binding proteins are components of a nuclear matrix-attachment site
dc.typeJournal Article
dc.source.journaltitleProceedings of the National Academy of Sciences of the United States of America
dc.source.volume89
dc.source.issue9
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/gsbs_sp/336
dc.identifier.contextkey619048
html.description.abstract<p>We have identified a nuclear matrix-attachment region within an upstream element of a human H4 histone gene promoter. Nuclear matrix proteins, isolated and solubilized from HeLa S3 cells, were found to interact with sequence specificity at this matrix-attachment region. Several types of assays for protein-DNA interaction showed that the minimal sequence for the nuclear matrix protein-DNA interaction was 5'-TGACGTCCATG-3'; the underlined region corresponds to the core consensus sequence for ATF transcription factor binding. Two proteins with molecular masses of 43 and 54 kDa were identified by UV-crosslinking analysis as integral components of this protein-DNA complex. The molecular masses of these proteins and the ATF-binding site consensus sequence suggest that these proteins are members of the ATF family. Our results provide direct evidence for nuclear matrix localization of sequence-specific DNA-binding factors for an actively transcribed gene. The proximity of a strong positive transcriptional regulatory element to the matrix-attachment region of this gene suggests that the nuclear matrix may serve to localize and concentrate trans-acting factors that facilitate regulation of gene expression.</p>
dc.identifier.submissionpathgsbs_sp/336
dc.contributor.departmentDepartment of Cell Biology
dc.contributor.departmentGraduate School of Biomedical Sciences
dc.source.pages4178-82


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