English  |  正體中文  |  简体中文  |  全文笔数/总笔数 : 21921/27947 (78%)
造访人次 : 4246902      在线人数 : 384
RC Version 6.0 © Powered By DSPACE, MIT. Enhanced by NTU Library IR team.
搜寻范围 查询小技巧:
  • 您可在西文检索词汇前后加上"双引号",以获取较精准的检索结果
  • 若欲以作者姓名搜寻,建议至进阶搜寻限定作者字段,可获得较完整数据
  • 进阶搜寻


    jsp.display-item.identifier=請使用永久網址來引用或連結此文件: http://140.128.103.80:8080/handle/310901/20276


    题名: 果蠅Jak/STAT訊息傳遞鏈中配體和受體間 的交互關係及功能之研究
    其它题名: Functional study of the interaction between ligands and receptors in Drosophila Jak/STAT pathway
    作者: 王柏凱
    Wang, Pokai
    贡献者: 蔡玉真
    Tsai, Yuchen
    東海大學生命科學系
    关键词: Jak/STAT訊息傳遞鏈;配體和受體的交互作用
    Jak/STA signaling;Ligands and receptors interaction
    日期: 2012
    上传时间: 2013-01-02T09:02:28Z (UTC)
    摘要: Jak/STAT訊息鏈調控多種生理反應,包含細胞增生、幹細胞維持、免疫反應和造血作用。當Jak/STAT訊息鏈失去妥善調控,可能會引發癌症和免疫相關的疾病。果蠅的Jak/STAT訊息鏈在演化上與哺乳動物同源且較為簡單,所以果蠅是良好的模式生物來研究Jak/STAT訊息鏈的功能。果蠅的Jak/STAT訊息鏈調控許多重要發育過程和生理反應。在果蠅的Jak/STAT訊息鏈中,三個Upd-like配體(Upd、Upd2、Upd3)及兩個Dome受體(Dome、Domelike)的下游,僅只有一個Jak和一個STAT,但可以調控許多發育過程及生理反應。最近的研究中發現,Dome和Domelike會形成同雙體及異雙體。在我的實驗中,利用免疫共沉澱法發現Upd-like蛋白也會形成同雙體及異雙體。我們推測在Jak/STAT訊息鏈中Upd-like蛋白形成雙體,可能會影響Upd-likes在組織中的分布,或改變和Dome受體的親和力,進而執行不同功能。另一方面,我發現在Upd-like蛋白中,Upd和Upd3不論在組織中的分布情形及長距離活化Jak/STAT活性的能力都很相近,而Upd2的特性較為不同。我也發現在果蠅眼碟表達不同組合的Upd-like配體時,會對複眼表型產生不同的影響。在觀察同時表達Upd-like配體和Dome受體對複眼發育的影響時,我發現表達Upd3時,複眼變大的性狀對於Dome受體的劑量很敏感,此外我也發現分別表達Upd和Upd3配合不同的Dome受體會造成果蠅複眼不同的性狀。此研究使我們對於果蠅Jak/STAT訊息鏈中配體和受體的作用機制有更深一層的了解,也透過對於果蠅這個模式生物的研究,我們能更了解哺乳動物Jak/STAT訊息鏈可能的作用機制。
    The Jak/STAT pathway plays a crucial role in physiological and developmental processes in mammals, such as immune response, hematopoiesis, and adipogenesis. Since the Jak/STAT signaling is evolutionarily conserved and Drosophila has only one Jak and one STAT, Drosophila is a simple and non-redundant system to investigate function and regulation of Jak/STAT pathway in vivo. Three ligands, Unpaired (Upd), Upd2, Upd3 and two receptors, Domeless (Dome) and Domelike, have been identified in Drosophila. Upd is regarded as an essential factor to affect cell proliferation, cell migration and differentiation whereas Upd3 is implicated in immune response. The function of upd2, however, remains obscure. On the other hand, it is suggested in recent studies that Dome and Domelike can form homodimers and heterodimers in vivo. Hence, we are interested in how such a simple Jak/STAT signaling regulates multiple distinct developmental processes. We proposed that different combinations of Upd-likes and Dome receptors would have different affinity and induce different biological effects. In my study, I found Upd-like proteins have different properties. Both Upd and Upd3 are N-linked glycoproteins, but Upd2 is not. The localization of Upd2 in vivo is also different from that of Upd and Upd3. Upd and Upd3 can influence Jak/STAT activity in a long-range manner, but Upd2 cannot. From the Co-immunoprecipitation assay, I found Upd-like proteins can form homodimers and heterodimers in S2 cells. The adult eye phenotype of Upd/Upd3 combination is different from Upd or Upd3. Also, different combinations of Upd-likes and Dome receptors have different effects on Drosophila eye development. This study may help us to further understand the molecular mechanism of ligands-receptors interaction in Drosophila Jak/STAT pathway.
    显示于类别:[生命科學系所] 碩博士論文

    文件中的档案:

    档案 大小格式浏览次数
    100THU00112019-001.pdf6545KbAdobe PDF412检视/开启


    在THUIR中所有的数据项都受到原著作权保护.


    本網站之東海大學機構典藏數位內容,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。

    DSpace Software Copyright © 2002-2004  MIT &  Hewlett-Packard  /   Enhanced by   NTU Library IR team Copyright ©   - 回馈