Source:http://linkedlifedata.com/resource/pubmed/id/18257392
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
|
pubmed:dateCreated |
2008-2-8
|
pubmed:abstractText |
The large zinc finger proteins, ZAS, regulate the transcription of a variety of genes involved in cell growth, development, and metastasis. They also function in the signal transduction of the TGF-beta and TNF-alpha pathways. However, the endogenous protein of a representative member, ZAS3, is rapidly degraded in primary lymphocytes, which limits the determination of its physiological function in vitro. Therefore, we have generated mice with targeted disruption of ZAS3. Oligonucleotide-based microarray analyses revealed subtle but consistent differences in the expression of genes, many of which are associated with receptor or signal transduction activities between ZAS3+/+ and ZAS3-/- thymi. Gel mobility shift assays showed altered DNA binding activities of NF-kappaB and AP-1 proteins in ZAS3-deficient tissues, including the thymus. Lymphocyte analysis suggested a subtle but broad function of ZAS3 in regulating T-cell development and activation. In CD3+ ZAS3-/- thymocytes, the CD4/ CD8 ratio was decreased and CD69 expression was decreased. In peripheral CD4+ ZAS3-/- lymphocytes we observed an increased number of memory T cells.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/DNA,
http://linkedlifedata.com/resource/pubmed/chemical/DNA Primers,
http://linkedlifedata.com/resource/pubmed/chemical/DNA-Binding Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/NF-kappa B,
http://linkedlifedata.com/resource/pubmed/chemical/Transcription Factor AP-1,
http://linkedlifedata.com/resource/pubmed/chemical/Transcription Factors,
http://linkedlifedata.com/resource/pubmed/chemical/ZAS3 protein, mouse
|
pubmed:status |
MEDLINE
|
pubmed:issn |
1052-2166
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
14
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
83-100
|
pubmed:meshHeading |
pubmed-meshheading:18257392-Animals,
pubmed-meshheading:18257392-Base Sequence,
pubmed-meshheading:18257392-Blotting, Southern,
pubmed-meshheading:18257392-Cell Proliferation,
pubmed-meshheading:18257392-DNA,
pubmed-meshheading:18257392-DNA Primers,
pubmed-meshheading:18257392-DNA-Binding Proteins,
pubmed-meshheading:18257392-Electrophoretic Mobility Shift Assay,
pubmed-meshheading:18257392-Mice,
pubmed-meshheading:18257392-Mice, Inbred C57BL,
pubmed-meshheading:18257392-Mice, Knockout,
pubmed-meshheading:18257392-NF-kappa B,
pubmed-meshheading:18257392-Oligonucleotide Array Sequence Analysis,
pubmed-meshheading:18257392-Polymerase Chain Reaction,
pubmed-meshheading:18257392-T-Lymphocytes,
pubmed-meshheading:18257392-Transcription Factor AP-1,
pubmed-meshheading:18257392-Transcription Factors
|
pubmed:year |
2007
|
pubmed:articleTitle |
Disruption of ZAS3 in mice alters NF-kappaB and AP-1 DNA binding and T-cell development.
|
pubmed:affiliation |
Department of Pediatrics and Center for Cell and Developmental Biology, Columbus Children's Research Institute, Columbus, OH 43205, USA.
|
pubmed:publicationType |
Journal Article
|