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dc.contributor.authorFrenkel, Baruch
dc.contributor.authorMijnes, Jolanda
dc.contributor.authorAronow, Michael A.
dc.contributor.authorZambetti, Gerard
dc.contributor.authorBanerjee, Chaitali
dc.contributor.authorStein, Janet L.
dc.contributor.authorLian, Jane B.
dc.contributor.authorStein, Gary S.
dc.date2022-08-11T08:08:57.000
dc.date.accessioned2022-08-23T16:13:43Z
dc.date.available2022-08-23T16:13:43Z
dc.date.issued1993-12-14
dc.date.submitted2008-09-10
dc.identifier.citation<p>Biochemistry. 1993 Dec 14;32(49):13636-43.</p>
dc.identifier.issn0006-2960 (Print)
dc.identifier.doi10.1021/bi00212a031
dc.identifier.pmid7504955
dc.identifier.urihttp://hdl.handle.net/20.500.14038/33691
dc.description.abstractOsteocalcin (OC) is a bone-specific protein which is expressed postproliferatively by osteoblasts during late stages of differentiation. We have found that a silencer element is present within the rat OC gene (between nt +39 and +104), overlapping the OC signal prepropeptide-coding sequence. The presence of this sequence in OC promoter-CAT reporter constructs suppresses promoter activity in transiently transfected proliferating osteoblasts, which do not express OC, by up to 50-fold. This is the first demonstration of contribution from protein-coding sequences to silencing of animal genes. The element appears to be bipartite; silencer activity requires both the protein-coding sequence +39 to +63 and the +93 to +104 exon 1/intron 1 border region. Both of these domains contain sequences highly similar to silencer motifs in several other genes, including chicken lysozyme as well as rat collagen type II, insulin, and growth hormone. OC silencer activity is fully retained when the element is placed outside the RNA-coding region, 3' but not 5' of the OC-CAT fusion gene. Repression activity is orientation independent in the native position but requires the native orientation when located in 3' extragenic positions. The silencer does not inhibit the activity of the heterologous SV40 early promoter. These results suggest interaction between the transcribed silencer and specific OC promoter element(s) residing farther upstream. The OC transcribed silencer may contribute to developmental control of OC 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=7504955&dopt=Abstract">Link to article in PubMed</a></p>
dc.relation.urlhttp://doi.org/10.1021/bi00212a031
dc.subjectAnimals; Base Sequence; Cells, Cultured; Chloramphenicol O-Acetyltransferase; Embryo, Mammalian; Exons; Genes, Reporter; Molecular Sequence Data; Osteoblasts; Osteocalcin; Promoter Regions (Genetics); RNA; Rats; *Regulatory Sequences, Nucleic Acid; Repetitive Sequences, Nucleic Acid; Transfection
dc.subjectLife Sciences
dc.subjectMedicine and Health Sciences
dc.titlePosition and orientation-selective silencer in protein-coding sequences of the rat osteocalcin gene
dc.typeJournal Article
dc.source.journaltitleBiochemistry
dc.source.volume32
dc.source.issue49
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/gsbs_sp/356
dc.identifier.contextkey625982
html.description.abstract<p>Osteocalcin (OC) is a bone-specific protein which is expressed postproliferatively by osteoblasts during late stages of differentiation. We have found that a silencer element is present within the rat OC gene (between nt +39 and +104), overlapping the OC signal prepropeptide-coding sequence. The presence of this sequence in OC promoter-CAT reporter constructs suppresses promoter activity in transiently transfected proliferating osteoblasts, which do not express OC, by up to 50-fold. This is the first demonstration of contribution from protein-coding sequences to silencing of animal genes. The element appears to be bipartite; silencer activity requires both the protein-coding sequence +39 to +63 and the +93 to +104 exon 1/intron 1 border region. Both of these domains contain sequences highly similar to silencer motifs in several other genes, including chicken lysozyme as well as rat collagen type II, insulin, and growth hormone. OC silencer activity is fully retained when the element is placed outside the RNA-coding region, 3' but not 5' of the OC-CAT fusion gene. Repression activity is orientation independent in the native position but requires the native orientation when located in 3' extragenic positions. The silencer does not inhibit the activity of the heterologous SV40 early promoter. These results suggest interaction between the transcribed silencer and specific OC promoter element(s) residing farther upstream. The OC transcribed silencer may contribute to developmental control of OC expression.</p>
dc.identifier.submissionpathgsbs_sp/356
dc.contributor.departmentDepartment of Orthopedic Surgery
dc.contributor.departmentDepartment of Cell Biology
dc.contributor.departmentGraduate School of Biomedical Sciences
dc.source.pages13636-43


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