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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/123456789/4997
完整後設資料紀錄
DC 欄位值語言
dc.contributor.advisor陳小梨
dc.contributor.authorWei-Chen Liuen
dc.contributor.author劉未辰zh_TW
dc.date.accessioned2021-05-15T17:50:50Z-
dc.date.available2014-10-09
dc.date.available2021-05-15T17:50:50Z-
dc.date.copyright2014-10-09
dc.date.issued2014
dc.date.submitted2014-08-19
dc.identifier.citation1. zur Hausen H (2009) Papillomaviruses in the causation of human cancers - a brief historical account. Virology 384: 260-265.
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protein, activates calcineurin to dephosphorylate human papillomavirus E2
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required for e2-mediated transcriptional activation but not genome
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bovine papillomavirus E2 protein with Brd4 tethers the viral DNA to host
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protein Brd4 binds to acetylated chromatin during interphase and mitosis.
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binding activity of the papillomavirus E2 protein correlates with interaction
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8920-8932.
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of papillomavirus E2-mediated plasmid maintenance in Saccharomyces
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2998-3003.
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enhances viral genome loss and phenotypic reversion of bovine
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DNA-tethering complex E2:Brd4 and a peptide that ablates HPV chromosomal
association. Mol Cell 24: 877-889.
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bromodomain protein Brd4 interaction using bimolecular fluorescence
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the human papillomavirus type 16 DNA replication complex is essential for
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papillomavirus type 8 E2 protein to host chromosomes. J Virol 86: 33
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overexpression of bromodomain-containing protein 4. J Virol 83: 4127-4139.
33. Lee AY, Chiang CM (2009) Chromatin adaptor Brd4 modulates E2 transcription
activity and protein stability. J Biol Chem 284: 2778-2786.
34. Nishiyama A, Dey A, Miyazaki J, Ozato K (2006) Brd4 is required for recovery from
antimicrotubule drug-induced mitotic arrest: preservation of acetylated
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to promote G1 gene expression and cell cycle progression. Mol Cell Biol 28:
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papillomavirus type 16 E2 interaction with chromatin. J Virol 81: 4338-4342.
37. Gammoh N, Grm HS, Massimi P, Banks L (2006) Regulation of human
papillomavirus type 16 E7 activity through direct protein interaction with the
E2 transcriptional activator. J Virol 80: 1787-1797.
38. Zheng PS, Brokaw J, McBride AA (2005) Conditional mutations in the mitotic
chromosome binding function of the bovine papillomavirus type 1 E2 protein.
J Virol 79: 1500-1509.
Abroi A, Ilves I, Kivi S, Ustav M (2004) Analysis of chromatin attachment and
partitioning functions of bovine papillomavirus type 1 E2 protein. J Virol 78:
2100-2113.
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papillomavirus E2 onto mitotic chromosomes and viral genome maintenance.
Mol Cell 24: 867-876.
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localization of the human papillomavirus type 11 origin binding protein E2
through mitosis while in association with the spindle apparatus. J Virol 80: 34
4792-4800.
42. Yu T, Peng YC, Androphy EJ (2007) Mitotic kinesin-like protein 2 binds and
colocalizes with papillomavirus E2 during mitosis. J Virol 81: 1736-1745.
43. Senechal H, Poirier GG, Coulombe B, Laimins LA, Archambault J (2007) Amino
acid substitutions that specifically impair the transcriptional activity of
papillomavirus E2 affect binding to the long isoform of Brd4. Virology 358:
10-17.
44. Zheng G, Schweiger MR, Martinez-Noel G, Zheng L, Smith JA, et al. (2009) Brd4
regulation of papillomavirus protein E2 stability. J Virol 83: 8683-8692.
45. Penrose KJ, McBride AA (2000) Proteasome-mediated degradation of the
papillomavirus E2-TA protein is regulated by phosphorylation and can
modulate viral genome copy number. J Virol 74: 6031-6038.
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348-357.
dc.identifier.urihttp://tdr.lib.ntu.edu.tw/jspui/handle/123456789/4997-
dc.description.abstract人類乳突瘤病毒(Human papillomavirus,HPV)的E2蛋白對病毒生命週期有著重要的影響。E2蛋白會影響病毒的複製,轉錄和segregation。之前大量研究表明E2蛋白在細胞分裂時鏈接病毒DNA與宿主染色體,使病毒DNA可以均勻分佈到兩顆細胞。根據前人研究得知人類乳突瘤病毒8型E2蛋白的S253位置的磷酸化會消失會導致E2蛋白在宿主細胞細胞分裂時不能與染色體鏈接。其中一個人類乳突瘤病毒16型E2蛋白上的磷酸化位置S243。其磷酸化的消失會使大部分E2蛋白在細胞分裂時從染色體脫落。並且其影響E2蛋白與染色體鏈接的能力是通過(Bromodomain-containing protein 4 )Brd4實現的。zh_TW
dc.description.provenanceMade available in DSpace on 2021-05-15T17:50:50Z (GMT). No. of bitstreams: 1
ntu-103-R00445129-1.pdf: 1862245 bytes, checksum: 1a45131f9120632578792eabd940a37f (MD5)
Previous issue date: 2014
en
dc.description.tableofcontents口試委員會審定書
序言 I
中文摘要 II
ABSTRACT III
第一章 緒論 1
第二章 材料和方法 4
第三章 試驗結果 6
第四章 討論 9
參考文獻 12
表格圖片 17
附錄 22
dc.language.isozh-TW
dc.subject磷酸化zh_TW
dc.subject人類乳突瘤病毒zh_TW
dc.subject染色體zh_TW
dc.subjectBrd4en
dc.subjectphosphorylationen
dc.subjectsegregationen
dc.subjectHPV16en
dc.title人類乳突瘤病毒16型 通過E2蛋白質S243磷酸化修飾調節與Brd4及宿主染色體連接zh_TW
dc.titlePhosphorylation of HPV-16 E2 at serine 243 enables binding to Brd4 and mitotic chromosomesen
dc.typeThesis
dc.date.schoolyear102-2
dc.description.degree碩士
dc.contributor.oralexamcommittee陳美如,詹迺立
dc.subject.keyword人類乳突瘤病毒,磷酸化,染色體,zh_TW
dc.subject.keywordHPV16,Brd4,phosphorylation,segregation,en
dc.relation.page23
dc.rights.note同意授權(全球公開)
dc.date.accepted2014-08-19
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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