Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
15
pubmed:dateCreated
1999-8-16
pubmed:databankReference
pubmed:abstractText
The POU-IV or Brn-3 class of transcription factors exhibit conserved structure, DNA-binding properties, and expression in specific subclasses of neurons across widely diverged species. In the mouse CNS, Brn-3.0 expression characterizes specific neurons from neurogenesis through the life of the cell. This irreversible activation of expression suggests positive autoregulation. To search for cis-acting elements that could mediate autoregulation we used a novel method, complex stability screening, which we applied to rapidly identify functional Brn-3.0 recognition sites within a large genomic region encompassing the mouse brn-3.0 locus. This method is based on the observation that the kinetic stability of Brn-3.0 complexes with specific DNA sequences, as measured by their dissociation half-lives, is highly correlated with the ability of those sequences to mediate transcriptional activation by Brn-3.0. The principal Brn-3.0 autoregulatory region lies approximately 5 kb upstream from the Brn-3.0 transcription start site and contains multiple Brn-3.0-binding sites that strongly resemble the optimal binding site for this protein class. This region also mediates transactivation by the closely related protein Brn-3.2, suggesting a regulatory cascade of POU proteins in specific neurons in which Brn-3.2 expression precedes Brn-3.0.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Aug
pubmed:issn
0270-6474
pubmed:author
pubmed:issnType
Print
pubmed:day
1
pubmed:volume
19
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
6549-58
pubmed:dateRevised
2008-11-21
pubmed:meshHeading
pubmed-meshheading:10414983-Aging, pubmed-meshheading:10414983-Animals, pubmed-meshheading:10414983-Chromosome Mapping, pubmed-meshheading:10414983-DNA, pubmed-meshheading:10414983-DNA-Binding Proteins, pubmed-meshheading:10414983-Drug Stability, pubmed-meshheading:10414983-Embryo, Mammalian, pubmed-meshheading:10414983-Embryonic and Fetal Development, pubmed-meshheading:10414983-Genetic Techniques, pubmed-meshheading:10414983-Genome, pubmed-meshheading:10414983-Homeodomain Proteins, pubmed-meshheading:10414983-Homeostasis, pubmed-meshheading:10414983-Immunohistochemistry, pubmed-meshheading:10414983-Mice, pubmed-meshheading:10414983-Time Factors, pubmed-meshheading:10414983-Transcription Factor Brn-3, pubmed-meshheading:10414983-Transcription Factor Brn-3A, pubmed-meshheading:10414983-Transcription Factor Brn-3B, pubmed-meshheading:10414983-Transcription Factors, pubmed-meshheading:10414983-Transcriptional Activation
pubmed:year
1999
pubmed:articleTitle
Autoregulatory sequences are revealed by complex stability screening of the mouse brn-3.0 locus.
pubmed:affiliation
Department of Psychiatry, University of California San Diego, La Jolla, California 92093-0603, USA.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, U.S. Gov't, Non-P.H.S., Research Support, Non-U.S. Gov't