pubmed-article:12949905 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:12949905 | lifeskim:mentions | umls-concept:C0087111 | lld:lifeskim |
pubmed-article:12949905 | lifeskim:mentions | umls-concept:C0085828 | lld:lifeskim |
pubmed-article:12949905 | lifeskim:mentions | umls-concept:C0019564 | lld:lifeskim |
pubmed-article:12949905 | lifeskim:mentions | umls-concept:C0205147 | lld:lifeskim |
pubmed-article:12949905 | lifeskim:mentions | umls-concept:C1171362 | lld:lifeskim |
pubmed-article:12949905 | lifeskim:mentions | umls-concept:C1819716 | lld:lifeskim |
pubmed-article:12949905 | lifeskim:mentions | umls-concept:C0040648 | lld:lifeskim |
pubmed-article:12949905 | lifeskim:mentions | umls-concept:C0017262 | lld:lifeskim |
pubmed-article:12949905 | lifeskim:mentions | umls-concept:C1515670 | lld:lifeskim |
pubmed-article:12949905 | lifeskim:mentions | umls-concept:C1145667 | lld:lifeskim |
pubmed-article:12949905 | lifeskim:mentions | umls-concept:C0205812 | lld:lifeskim |
pubmed-article:12949905 | lifeskim:mentions | umls-concept:C0591833 | lld:lifeskim |
pubmed-article:12949905 | pubmed:issue | 6 | lld:pubmed |
pubmed-article:12949905 | pubmed:dateCreated | 2003-9-1 | lld:pubmed |
pubmed-article:12949905 | 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. | lld:pubmed |
pubmed-article:12949905 | pubmed:language | eng | lld:pubmed |
pubmed-article:12949905 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:12949905 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:12949905 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:12949905 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:12949905 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:12949905 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:12949905 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:12949905 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:12949905 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:12949905 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:12949905 | pubmed:month | Sep | lld:pubmed |
pubmed-article:12949905 | pubmed:issn | 0360-4012 | lld:pubmed |
pubmed-article:12949905 | pubmed:author | pubmed-author:YonedaYukioY | lld:pubmed |
pubmed-article:12949905 | pubmed:author | pubmed-author:OgitaKiyokazu... | lld:pubmed |
pubmed-article:12949905 | pubmed:author | pubmed-author:KitanoMasahir... | lld:pubmed |
pubmed-article:12949905 | pubmed:author | pubmed-author:FujinamiYoshi... | lld:pubmed |
pubmed-article:12949905 | pubmed:copyrightInfo | Copyright 2003 Wiley-Liss, Inc. | lld:pubmed |
pubmed-article:12949905 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:12949905 | pubmed:day | 15 | lld:pubmed |
pubmed-article:12949905 | pubmed:volume | 73 | lld:pubmed |
pubmed-article:12949905 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:12949905 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:12949905 | pubmed:pagination | 794-802 | lld:pubmed |
pubmed-article:12949905 | pubmed:dateRevised | 2008-11-21 | lld:pubmed |
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pubmed-article:12949905 | pubmed:year | 2003 | lld:pubmed |
pubmed-article:12949905 | pubmed:articleTitle | Transcription factor activator protein-1 expressed by kainate treatment can bind to the non-coding region of mitochondrial genome in murine hippocampus. | lld:pubmed |
pubmed-article:12949905 | pubmed:affiliation | Department of Pharmacology, Faculty of Pharmaceutical Sciences, Setsunan University, Hirakata, Osaka, Japan. ogita@pharm.setsunan.ac.jp | lld:pubmed |
pubmed-article:12949905 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:12949905 | pubmed:publicationType | Comparative Study | lld:pubmed |
pubmed-article:12949905 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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