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DNA Sequences in the Promoter Region of the NF1 Gene Are Highly Conserved between Human and Mouse

dc.contributor.authorHajra, Amitaven_US
dc.contributor.authorMartin-Gallardo, Antoniaen_US
dc.contributor.authorTarle, Susan A.en_US
dc.contributor.authorFreedman, Matthew L.en_US
dc.contributor.authorWilson-Gunn, Susanen_US
dc.contributor.authorBernards, Andreen_US
dc.contributor.authorCollins, Francis S.en_US
dc.date.accessioned2006-04-10T18:07:40Z
dc.date.available2006-04-10T18:07:40Z
dc.date.issued1994-06en_US
dc.identifier.citationHajra, Amitav, Martin-Gallardo, Antonia, Tarle, Susan A., Freedman, Matthew, Wilson-Gunn, Susan, Bernards, Andre, Collins, Francis S. (1994/06)."DNA Sequences in the Promoter Region of the NF1 Gene Are Highly Conserved between Human and Mouse." Genomics 21(3): 649-652. <http://hdl.handle.net/2027.42/31556>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6WG1-45NJXTN-3D/2/94a761efad78ad6306d4f3f8acf4388den_US
dc.identifier.urihttps://hdl.handle.net/2027.42/31556
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=7959746&dopt=citationen_US
dc.description.abstractThe gene for type 1 neurofibromatosis (NF1) is most highly expressed in brain and spinal cord, although low levels of mRNA can be found in nearly all tissues. As a first step in investigating the regulation of NF1 gene expression, we have cloned and sequenced the promoter regions of the human and mouse NF1 genes and mapped the transcriptional start sites in both species. We report here that the 5' ends of the human and murine NF1 genes are highly conserved. While no discernable TATA or CCAAT box sequences are seen, transcription initiates at identical sites in both species, 484 nucleotides upstream of the ATG initiation codon in the human gene. The human and mouse NF1 genes share particularly high sequence homology (95%) between nucleotides -33 and +261 and contain several perfectly conserved transcription factor binding site motifs, including a cAMP response element, several AP2 consensus binding sites, and a serum response element. The high conservation of these sequences indicates that they are likely to be significant in the regulation of NF1 gene expression.en_US
dc.format.extent290085 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleDNA Sequences in the Promoter Region of the NF1 Gene Are Highly Conserved between Human and Mouseen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelMolecular, Cellular and Developmental Biologyen_US
dc.subject.hlbsecondlevelGeneticsen_US
dc.subject.hlbsecondlevelBiological Chemistryen_US
dc.subject.hlbtoplevelScienceen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartments of Human Genetics and Internal Medicine and the Howard Hughes Medical Institute, University of Michigan, Ann Arbor, Michigan, USA.en_US
dc.contributor.affiliationumDepartments of Human Genetics and Internal Medicine and the Howard Hughes Medical Institute, University of Michigan, Ann Arbor, Michigan, USA.en_US
dc.contributor.affiliationumDepartments of Human Genetics and Internal Medicine and the Howard Hughes Medical Institute, University of Michigan, Ann Arbor, Michigan, USA.en_US
dc.contributor.affiliationumDepartments of Human Genetics and Internal Medicine and the Howard Hughes Medical Institute, University of Michigan, Ann Arbor, Michigan, USA.en_US
dc.contributor.affiliationumDepartments of Human Genetics and Internal Medicine and the Howard Hughes Medical Institute, University of Michigan, Ann Arbor, Michigan, USA.en_US
dc.contributor.affiliationotherCentro Nacional de Biotecnologia, 28049 Madrid, Spainen_US
dc.contributor.affiliationotherMassachusetts General Hospital Molecular Neurogenetics Unit and Cancer Center, Charlestown, Massachusetts, USA.en_US
dc.identifier.pmid7959746en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/31556/1/0000482.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1006/geno.1994.1328en_US
dc.identifier.sourceGenomicsen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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