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  1. NTU Theses and Dissertations Repository
  2. 醫學院
  3. 微生物學科所
請用此 Handle URI 來引用此文件: http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/41318
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dc.contributor.advisor戴榮湘
dc.contributor.authorLung-Chun Changen
dc.contributor.author張隆俊zh_TW
dc.date.accessioned2021-06-15T00:15:45Z-
dc.date.available2009-09-15
dc.date.copyright2009-09-15
dc.date.issued2009
dc.date.submitted2009-06-12
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47. Schwebke, J.R. and Burgess, D. (2004) Trichomoniasis. Clin. Microbiol. Rev. 17: 794-803.
48. Scott A. Ness. (2003) Myb protein specifity: evidence of a context-specific transcription factor code. Blood Cells, Molecules, and Diseases 31: 192-200.
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50. Shiou-Jeng Ong, Hong-Ming Hsu, Hsing-Wei Liu, and Jung-Hsiang Tai. (2004) Involvement of multiple DNA elements in iron-inducible transcription of the ap65-1 gene in the protozoan parasite Trichomonas vaginalis. Mol. Microbiol. 52: 1721-1730.
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68. 黃勝祈 (2002) 探討鐵離子及細胞生長對陰道滴蟲ap65-1啟動子的調控表現.台灣大學微生物學研究所寄生蟲學組碩士論文.
69. Clontech Laboratories, Inc. Living Colors® User Manual PT2040-1
dc.identifier.urihttp://tdr.lib.ntu.edu.tw/jspui/handle/123456789/41318-
dc.description.abstractMyb2調控陰道滴蟲ap65-1基因的轉錄活性,通常存在於細胞核中。本研究之目的在於尋找Myb2入核控制序列。利用免疫螢光染色方法,藉蛋白質刪短或突變技術,發現Myb2入核控制之充分序列位於區域48-143,其中以酸性胺基酸聚集區域55EEDE58為入核控制所必需,而51KF52、139NRW141與143T/S145亦可能參與Myb2之入核控制。Myb2核酸結合區域 (DNA-binding domain) R2R3中,若刪除H2、H3、H4、H5與RC4等任一結構元素,所表現之蛋白質均滯留於細胞質中;顯示分子結構之完整性可能亦為Myb2入核所需。由西方墨點法偵知,144-179區域可能為轉譯後修飾之標的;此修飾可能發生於細胞質中,與Myb2之入核無關。藉由有限的激酶抑制劑處理,無法偵測得Myb2入核的訊息傳遞路徑,而Myb2入核亦不受到因生長所引起之培養環境變化的影響。這些結果顯示陰道滴蟲Myb2的入核信號 (Nuclear Localization Signal)複雜,並非由單一序列所控制。zh_TW
dc.description.abstractMyb2, which regulates iron inducible transcription of the ap65-1 gene in the protozoan parasite Trichomonas vaginalis, was persistently detected in the nucleus. In the study, the nuclear localization signal of Myb2 was investgated exploiting immuneflouorescence assay to monitor subcellular localization of Myb2 and its mutant proteins. The region 48-143 was found to be sufficient, while 55EEDE58 as well as anyone of the structure elements in the R2R3 DNA-binding domain to be essential for nuclear import. Moreover, 51KF52, 139NRW141, and 143T/S145 together may also play important roles in Myb2 nuclear import. As examined by Western blotting, the region spanning 144-179 may contain a site for post-translational modification, which is not required for Myb2 nuclear import. Signal transduction pathway involve in Myb2 nuclear import were not identified. These observations suggest that Myb2 nuclear translocation is controlled by a novel nuclear localization signal.en
dc.description.provenanceMade available in DSpace on 2021-06-15T00:15:45Z (GMT). No. of bitstreams: 1
ntu-98-R95445205-1.pdf: 1310868 bytes, checksum: 7016e2498858f4f218915ddd885cd316 (MD5)
Previous issue date: 2009
en
dc.description.tableofcontents縮寫表..............................................................1
中文摘要............................................................2
英文摘要............................................................3
前言................................................................4
一、簡介..........................................................4
二、陰道滴蟲之基因體..............................................4
三、Myb轉錄因子..................................................4
四、鐵離子對陰道滴蟲的影響.........................................6
五、轉錄因子的入核運輸.............................................7
材料與方法.........................................................10
一、陰道滴蟲細胞株的培養及處理....................................10
二、質體構築與轉染................................................10
三、聚丙烯醯胺膠體電泳............................................11
四、西方墨點法....................................................11
五、免疫螢光染色法................................................11
結果...............................................................13
一、建立4HA-Myb2表現系統........................................13
二、Myb2入核控制區域.............................................13
三、控制Myb2入核之胺基酸........................................13
四、Myb2立體結構.................................................14
五、不同建構之Myb2分子大小......................................14
六、調控Myb2入核之因子..........................................15
七、抑制劑對Myb2入核的影響......................................15
八、細胞周期對Myb2入核的影響....................................15

討論...............................................................17
一、重要入核控制區域..............................................17
二、重要入核控制序列..............................................17
三、Myb2結構.....................................................19
四、控制Myb2入核的機制..........................................19
五、Myb2的表現...................................................20
附表...............................................................21
附圖...............................................................31
參考文獻...........................................................55
附錄...............................................................63
dc.language.isozh-TW
dc.subjectTrichomonas vaginalisen
dc.subjectWestern blot assayen
dc.subjectimmuno-fluorescence assayen
dc.subjectpoint mutation and truncationen
dc.subjectnuclear localization signalen
dc.subjectMyb2en
dc.title探討陰道滴蟲Myb2蛋白質中調控入核運輸之區域zh_TW
dc.titleDefine the nuclear translocation domain of Myb2 protein in Trichomonas vaginalisen
dc.typeThesis
dc.date.schoolyear97-2
dc.description.degree碩士
dc.contributor.oralexamcommittee翁秀貞,許翠瑛
dc.subject.keyword陰道滴蟲,Myb2轉錄因子,入核控制序列,胺基酸突變及刪短,免疫螢光染色實驗,西方墨點實驗,zh_TW
dc.subject.keywordTrichomonas vaginalis,Myb2,nuclear localization signal,point mutation and truncation,immuno-fluorescence assay,Western blot assay,en
dc.relation.page65
dc.rights.note有償授權
dc.date.accepted2009-06-12
dc.contributor.author-college醫學院zh_TW
dc.contributor.author-dept微生物學研究所zh_TW
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