English  |  正體中文  |  简体中文  |  Post-Print筆數 : 27 |  Items with full text/Total items : 113303/144284 (79%)
Visitors : 50797097      Online Users : 705
RC Version 6.0 © Powered By DSPACE, MIT. Enhanced by NTU Library IR team.
Scope Tips:
  • please add "double quotation mark" for query phrases to get precise results
  • please goto advance search for comprehansive author search
  • Adv. Search
    HomeLoginUploadHelpAboutAdminister Goto mobile version
    Please use this identifier to cite or link to this item: https://nccur.lib.nccu.edu.tw/handle/140.119/76068


    Title: Novel role and mechanism of protein inhibitor of activated STAT1 in spatial learning
    Authors: Tai, D.J.C.;Hsu, W.L.;Liu, Yen-Chi;Ma, Y.L.;Lee, E.H.Y.
    Contributors: 神經科學研究所
    Keywords: complementary DNA;DNA binding protein;DNA fragment;protein inhibitor of activated STAT1;small interfering RNA;STAT1 protein;transcription factor;tyrosine;unclassified drug;animal cell;animal experiment;animal tissue;article;central nervous system;controlled study;facilitation;gene expression;genetic transfection;hippocampal CA1 region;learning;male;maze test;nerve cell;nonhuman;plasmid;polymerase chain reaction;priority journal;protein function;protein phosphorylation;protein processing;rat;spatial memory;sumoylation;water maze test;Animals;Cells, Cultured;DNA;Gene Expression Regulation;Hippocampus;Male;Maze Learning;Mutation;Phosphorylation;Protein Inhibitors of Activated STAT;Rats;Rats, Sprague-Dawley;RNA, Small Interfering;STAT1 Transcription Factor;Sumoylation;Transfection;Rattus
    Date: 2011-01
    Issue Date: 2015-06-23 15:48:50 (UTC+8)
    Abstract: By using differential display PCR, we have previously identified 98 cDNA fragments from rat dorsal hippocampus, which are expressed differentially between the fast learners and slow learners from water-maze learning task. One cDNA fragment, which showed a higher expression level in fast learners, encodes the rat protein inhibitor of activated STAT1 (pias1) gene. Spatial training induced a significant increase in PIAS1 expression in rat hippocampus. Transient transfection of the wild-type (WT) PIAS1 plasmid to CA1 neurons facilitated, whereas transfection of PIAS1 siRNA impaired spatial learning in rats. Meanwhile, PIAS1WT increased STAT1 sumoylation, decreased STAT1 DNA binding and decreased STAT1 phosphorylation at Tyr-701 associated with spatial learning facilitation. But PIAS1 siRNA transfection produced an opposite effect on these measures associated with spatial learning impairment. Further, transfection of STAT1 sumoylation mutant impaired spatial acquisition, whereas transfection of STAT1 phosphorylation mutant blocked the impairing effect of PIAS1 siRNA on spatial learning. In this study, we first demonstrate the role of PIAS1 in spatial learning. Both posttranslational modifications (increased sumoylation and decreased phosphorylation) mediate the effect of PIAS1 on spatial learning facilitation. © 2011 European Molecular Biology Organization | Some Rights Reserved.
    Relation: EMBO Journal, 30(1), 205-220
    Data Type: article
    DOI 連結: http://dx.doi.org/10.1038/emboj.2010.290
    DOI: 10.1038/emboj.2010.290
    Appears in Collections:[神經科學研究所] 期刊論文

    Files in This Item:

    File Description SizeFormat
    205.pdf1344KbAdobe PDF2931View/Open
    index.html0KbHTML21088View/Open


    All items in 政大典藏 are protected by copyright, with all rights reserved.


    社群 sharing

    著作權政策宣告 Copyright Announcement
    1.本網站之數位內容為國立政治大學所收錄之機構典藏,無償提供學術研究與公眾教育等公益性使用,惟仍請適度,合理使用本網站之內容,以尊重著作權人之權益。商業上之利用,則請先取得著作權人之授權。
    The digital content of this website is part of National Chengchi University Institutional Repository. It provides free access to academic research and public education for non-commercial use. Please utilize it in a proper and reasonable manner and respect the rights of copyright owners. For commercial use, please obtain authorization from the copyright owner in advance.

    2.本網站之製作,已盡力防止侵害著作權人之權益,如仍發現本網站之數位內容有侵害著作權人權益情事者,請權利人通知本網站維護人員(nccur@nccu.edu.tw),維護人員將立即採取移除該數位著作等補救措施。
    NCCU Institutional Repository is made to protect the interests of copyright owners. If you believe that any material on the website infringes copyright, please contact our staff(nccur@nccu.edu.tw). We will remove the work from the repository and investigate your claim.
    DSpace Software Copyright © 2002-2004  MIT &  Hewlett-Packard  /   Enhanced by   NTU Library IR team Copyright ©   - Feedback