Source:http://linkedlifedata.com/resource/pubmed/id/12949905
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
|
pubmed:dateCreated |
2003-9-1
|
pubmed:abstractText |
We have demonstrated previously that the transcription factor activator protein-1 (AP-1) complex is translocated into mitochondria into the nucleus in murine hippocampus after systemic kainate injection (Ogita et al. [2002] J. Neurosci. 22:2561-2570). The present study investigates whether the mitochondrial AP-1 complex translocated in response to kainate treatment binds to AP-1-like sites located at the non-coding region of the mitochondrial genome in mouse hippocampus. There are 10 sites with sequences similar to the nuclear AP-1 site in the non-coding region. Of 10 pieces (MT-1-MT-10) of synthesized double-stranded oligonucleotides, each containing a mitochondrial AP-1-like site, MT-3, MT-4, and MT-9 were effective in inhibiting mitochondrial AP-1 DNA binding enhanced by kainate. Electrophoresis mobility shift analysis using radiolabeled MT-3 and MT-9 probes demonstrated marked enhancement with binding of these 2 probes in hippocampal mitochondrial extracts prepared 2-6 hr after kainate treatment. Unlabeled AP-1 probe was more potent than unlabeled MT-9 probe in inhibiting the mitochondrial MT-9 binding. Supershift analysis revealed participation of particular Fos/Jun family proteins, such as c-Fos, Fos-B, c-Jun, Jun-B, and Jun-D, in MT-9 binding in hippocampal mitochondrial extracts prepared 4 hr after kainate treatment. Immunoprecipitation analysis using anti-c-Fos antibody demonstrated that c-Fos associated with the mitochondrial genome in hippocampal mitochondria prepared from kainate-treated animals. These results suggest that the AP-1 complex expressed by in vivo kainate treatment would bind to AP-1-like sites in the non-coding region of the mitochondrial genome after translocation into mitochondria from murine hippocampus.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Antibodies,
http://linkedlifedata.com/resource/pubmed/chemical/DNA-Binding Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Excitatory Amino Acid Agonists,
http://linkedlifedata.com/resource/pubmed/chemical/Exoribonucleases,
http://linkedlifedata.com/resource/pubmed/chemical/Kainic Acid,
http://linkedlifedata.com/resource/pubmed/chemical/Transcription Factor AP-1,
http://linkedlifedata.com/resource/pubmed/chemical/oligonucleotidase
|
pubmed:status |
MEDLINE
|
pubmed:month |
Sep
|
pubmed:issn |
0360-4012
|
pubmed:author | |
pubmed:copyrightInfo |
Copyright 2003 Wiley-Liss, Inc.
|
pubmed:issnType |
Print
|
pubmed:day |
15
|
pubmed:volume |
73
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
794-802
|
pubmed:dateRevised |
2008-11-21
|
pubmed:meshHeading |
pubmed-meshheading:12949905-Animals,
pubmed-meshheading:12949905-Antibodies,
pubmed-meshheading:12949905-Area Under Curve,
pubmed-meshheading:12949905-Binding, Competitive,
pubmed-meshheading:12949905-Binding Sites,
pubmed-meshheading:12949905-DNA-Binding Proteins,
pubmed-meshheading:12949905-Dose-Response Relationship, Drug,
pubmed-meshheading:12949905-Electrophoretic Mobility Shift Assay,
pubmed-meshheading:12949905-Excitatory Amino Acid Agonists,
pubmed-meshheading:12949905-Exoribonucleases,
pubmed-meshheading:12949905-Gene Expression Regulation,
pubmed-meshheading:12949905-Genome,
pubmed-meshheading:12949905-Hippocampus,
pubmed-meshheading:12949905-Kainic Acid,
pubmed-meshheading:12949905-Male,
pubmed-meshheading:12949905-Mice,
pubmed-meshheading:12949905-Mice, Inbred Strains,
pubmed-meshheading:12949905-Mitochondria,
pubmed-meshheading:12949905-Polymerase Chain Reaction,
pubmed-meshheading:12949905-Precipitin Tests,
pubmed-meshheading:12949905-Promoter Regions, Genetic,
pubmed-meshheading:12949905-Sequence Homology,
pubmed-meshheading:12949905-Time Factors,
pubmed-meshheading:12949905-Transcription Factor AP-1
|
pubmed:year |
2003
|
pubmed:articleTitle |
Transcription factor activator protein-1 expressed by kainate treatment can bind to the non-coding region of mitochondrial genome in murine hippocampus.
|
pubmed:affiliation |
Department of Pharmacology, Faculty of Pharmaceutical Sciences, Setsunan University, Hirakata, Osaka, Japan. ogita@pharm.setsunan.ac.jp
|
pubmed:publicationType |
Journal Article,
Comparative Study,
Research Support, Non-U.S. Gov't
|