請用此 Handle URI 來引用此文件:
http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/28576完整後設資料紀錄
| DC 欄位 | 值 | 語言 |
|---|---|---|
| dc.contributor.advisor | 鄧述諄(Shu-Chun Teng) | |
| dc.contributor.author | Ting-Wei Hung | en |
| dc.contributor.author | 洪頂瑋 | zh_TW |
| dc.date.accessioned | 2021-06-13T00:12:46Z | - |
| dc.date.available | 2007-08-08 | |
| dc.date.copyright | 2007-08-08 | |
| dc.date.issued | 2007 | |
| dc.date.submitted | 2007-07-27 | |
| dc.identifier.citation | 1. Lundblad, V. & Szostak, J. W. A mutant with a defect in telomere elongation leads to senescence in yeast. Cell 57, 633-643 (1989).
2. Garvik, B., Carson, M. & Hartwell, L. Single-stranded DNA arising at telomeres in cdc13 mutants may constitute a specific signal for the RAD9 checkpoint. Mol. Cell. Biol. 15, 6128-6138 (1995). 3. Grandin, N., Damon, C. & Charbonneau, M. Ten1 functions in telomere end protection and length regulation in association with Stn1 and Cdc13. EMBO J. 20, 1173-1183 (2001). 4. Grandin, N., Reed, S. I. & Charbonneau, M. Stn1, a new Saccharomyces cerevisiae protein, is implicated in telomere size regulation in association with Cdc13. Genes Dev. 11, 512-527 (1997). 5. van Steensel, B., Smogorzewska, A. & de Lange, T. TRF2 protects human telomeres from end-to-end fusions. Cell 92, 401-413 (1998). Shows that telomeric fusions occur when G-tails are lost in human cells, despite the presence of duplex telomeric DNA. 6. Chan CS, Tye BK. 1983. Organization of DNA sequences and replication origins at yeast telomeres. Cell 33: 563– 73 7. Zakian VA, Blanton HM. 1988. Distribution of telomere-associated sequences on natural chromosomes of Saccharomyces cerevisiae. Mol. Cell. Biol. 8: 2257– 60 8. Louis EJ, Naumova ES, Lee A, Naumov G, Haber JE. 1994. The chromosome end in yeast: its mosaic nature and influence on recombinational dynamics. Genetics 136: 789– 802 9. Louis EJ, Haber JE. 1990. The subtelomeric Y' repeat family in Saccharomyces cerevisiae: an experimental system for repeated sequence evolution. Genetics 124: 533– 45 10. Louis EJ, Haber JE. 1992. The structure and evolution of subtelomeric Y' repeats in Saccharomyces cerevisiae. Genetics 131: 559– 74 11. Watson JD. 1972. Nat. New Biol. 239: 197– 201 12. Olovnikov AM. 1973. J. Theor. Biol. 41: 181– 90 13. Lundblad V, Szostak JW. 1989. Cell 57: 633– 43 14. Levis RW. 1989. Cell 58: 791– 801 15. Johnson FB, Marciniak RA, McVey M, Stewart SA, Hahn WC, Guarente L. 2001. EMBO J. 20: 905– 13 16. Walter MF, Bozorgnia L, Maheshwari A, Biessmann H. 2001. Insect. Mol. Biol. 10: 105– 10 17. Niida H, Matsumoto T, Satoh H, Shiwa M, Tokutake Y, et al. 1998. Nat. Genet. 19: 203– 6 18. Blasco MA, Lee HW, Hande MP, Samper E, Lansdorp PM, et al. 1997. Cell 91: 25– 34 19. Harley CB, Futcher AB, Greider CW. 1990. Nature 345: 458– 60 20. Greider CW, Blackburn EH. 1985. Cell 43: 405– 13 21. Greider CW, Blackburn EH. 1987. Cell 51: 887– 98 22. Lingner, J. et al. Reverse transcriptase motifs in the catalytic subunit of telomerase. Science 276, 561-567 (1997). 23. Nakamura, T. M. et al. Telomerase catalytic subunit homologs from fission yeast and human. Science 277, 955-959 (1997). 24. Meyerson, M. et al. hEST2, the putative human telomerase catalytic subunit gene, is up-regulated in tumor cells and during immortalization. Cell 90, 785-795 (1997). 25. Singer, M. S. & Gottschling, D. E. TLC1, the template RNA component of the Saccharomyces cerevisiae telomerase. Science 266, 404-409 (1994). 26. Feng, J. et al. The RNA component of human telomerase. Science 269, 1236-1241 (1995). 27. Chakhparonian, M. & Wellinger, R. J. Telomere maintenance and DNA replication: how closely are these two connected? Trends Genet. 19, 439-446 (2003). 28. Nakamura TM, Morin GB, Chapman KB, Weinrich SL, Andrews WH, et al. 1997. Science 277: 955– 59 29. Meyerson M, Counter CM, Eaton EN, Ellisen LW, Steiner P, et al. 1997. Cell 90: 785– 95 30. Kim NW, Piatyszek MA, Prowse KR, Harley CB, West MD, et al. 1994. Science 266: 2011– 15 31. Steinert S, White DM, Zou Y, Shay JW, Wright WE. 2002. Exp. Cell Res. 272: 146– 52 32. Cong YS, Wright WE, Shay JW. 2002. Microbiol. Mol. Biol. Rev. 66: 407– 25 33. Feng J, Funk WD, Wang SS, Weinrich SL, Avilion AA, et al. 1995. Science 269: 1236– 41 34. Conrad, M. N., Wright, J. H., Wolf, A. J. & Zakian, V. A. RAP1 protein interacts with yeast telomeres in vivo: overproduction alters telomere structure and decreases chromosome stability. Cell 63, 739-750 (1990). 35. Chong, L. et al. A human telomeric protein. Science 270, 1663-1667 (1995). 36. Broccoli, D., Smogorzewska, A., Chong, L. & de Lange, T. Human telomeres contain two distinct Myb-related proteins, TRF1 and TRF2. Nature Genet. 17, 231-235 (1997). 37. Bourns, B. D., Alexander, M. K., Smith, A. M. & Zakian, V. A. Sir proteins, Rif proteins and Cdc13p bind Saccharomyces telomeres in vivo. Mol. Cell. Biol. 18, 5600-5608 (1998). 38. Tsukamoto, Y., Taggart, A. K. P. & Zakian, V. A. The role of the Mre11-Rad50-Xrs2 complex in telomerase-mediated lengthening of Saccharomyces cerevisiae telomeres. Curr. Biol. 11, 1328-1335 (2001). 39. Baumann, P. & Cech, T. R. Pot1, the putative telomere end-binding protein in fission yeast and humans. Science 292, 1171-1175 (2001). 40. Baumann, P., Podell, E. & Cech, T. R. Human Pot1 (protection of telomeres) protein: cytolocalization, gene structure, and alternative splicing. Mol. Cell. Biol. 22, 8079-8087 (2002). 41. Griffith, J. D. et al. Mammalian telomeres end in a large duplex loop. Cell 97, 503-514 (1999). 42. Strahl-Bolsinger, S., Hecht, A., Luo, K. & Grunstein, M. SIR2 and SIR4 interactions differ in core and extended telomeric heterochromatin in yeast. Genes Dev. 11, 83-93 (1997). 43. de Bruin, D., Zaman, Z., Liberatore, R. A. & Ptashne, M. Telomere looping permits gene activation by a downstream UAS in yeast. Nature 409, 109-113 (2001). 44. de Lange T. 2002. Oncogene 21: 532– 40 45. Blackburn EH. 2001. Cell 106: 661– 73 46. Hayflick, L. & Moorhead, P. S. The serial cultivation of human diploid cell strains. Exp. Cell Res. 25, 585-621 (1961). 47. Girardi, A. J., Jensen, F. C. & Koprowski, H. SV40-induced transformation of human diploid cells: crisis and recovery. J. Cell. Comp. Physiol. 65, 69-84 (1965). 48. Bryan, T. M. & Reddel, R. R. SV40-induced immortalization of human cells. Crit. Rev. Oncogenesis 5, 331-357 (1994). 49. Huschtscha, L. I. & Holliday, R. Limited and unlimited growth of SV40-transformed cells from human diploid MRC-5 fibroblasts. J. Cell Sci. 63, 77-99 (1983). 50. Shay, J. W. & Wright, W. E. Quantitation of the frequency of immortalization of normal human diploid fibroblasts by SV40 large T-antigen. Exp. Cell Res. 184, 109-118 (1989). 51. Counter, C. M. et al. Telomere shortening associated with chromosome instability is arrested in immortal cells which express telomerase activity. EMBO J. 11, 1921-1929 (1992). 52. Murnane, J. P., Sabatier, L., Marder, B. A. & Morgan, W. F. Telomere dynamics in an immortal human cell line. EMBO J. 13, 4953-4962 (1994). 53. Kim, N. W. et al. Specific association of human telomerase activity with immortal cells and cancer. Science 266, 2011-2015 (1994). 54. Bryan, T. M., Englezou, A., Gupta, J., Bacchetti, S. & Reddel, R. R. Telomere elongation in immortal human cells without detectable telomerase activity. EMBO J. 14, 4240-4248 (1995). 55. Bryan, T. M. & Reddel, R. R. Telomere dynamics and telomerase activity in in vitro immortalised human cells. Eur. J. Cancer 33, 767-773 (1997). 56. Shay, J. W. & Bacchetti, S. A survey of telomerase activity in human cancer. Eur. J. Cancer 33, 787-791 (1997). 57. Allshire RC, Dempster M, Hastie ND. (1989). Nucleic Acids Res., 17: 4611-4627. 58. de Lange T, Shiue L, Myers RM, Cox DR, Naylor SL, Killery AM, Varmus HE. (1990). Mol. Cell. Biol., 10: 518-527. 59. Bryan TM, Englezou A, Gupta J, Bacchetti S, Reddel RR. (1995). EMBO J., 14: 4240-4248. 60. de Lange T. (1995). Telomere dynamics and genome instability in human cancer. In Telomeres Blackburn EH, Greider CW (eds) Cold Spring Harbor Laboratory Press: New York, pp 265-293. 61. Park KH, Rha SY, Kim CH, Kim TS, Yoo NC, Kim JH, Roh JK, Noh SH, Min JS, Lee KS, Kim BS, Chung HC. (1998). Int. J. Oncol., 13: 489-495. 62. Bryan TM, Reddel RR. (1997). Eur. J. Cancer, 33: 767-773. 63. Grobelny JV, Godwin AK, Broccoli D. (2000). J. Cell Sci., 113: 4577-4585. 64. Murnane JP, Sabatier L, Marder BA, Morgan WF. (1994). EMBO J., 13: 4953-4962. 65. Opitz OG, Suliman Y, Hahn WC, Harada H, Blum HE, Rustgi AK. (2001). J. Clin. Invest., 108: 725-732. 66. Yeager TR, Neumann AA, Englezou A, Huschtscha LI, Noble JR, Reddel RR. (1999). Cancer Res., 59: 4175-4179. 67. Johnson FB, Marciniak RA, McVey M, Stewart SA, Hahn WC, Guarente L. (2001). EMBO J., 20: 905-913. 68. Wu G, Lee W-H, Chen P-L. (2000). J. Biol. Chem., 275: 30618-30622. 69. Yankiwski V, Marciniak RA, Guarente L, Neff NF. (2000). Proc. Natl. Acad. Sci. USA, 97: 5214-5219. 70. Yeager TR, Neumann AA, Englezou A, Huschtscha LI, Noble JR, Reddel RR. (1999). Cancer Res., 59: 4175-4179. 71. Zhu X-D, Küster B, Mann M, Petrini JHJ, de Lange T. (2000). Nat. Genet., 25: 347-352. 72. Perrem K, Colgin LM, Neumann AA, Yeager TR, Reddel RR. (2001). Mol. Cell. Biol., 21: 3862-3875. 73. Lundblad, V. & Blackburn, E. H. An alternative pathway for yeast telomere maintenance rescues est1- senescence. Cell 73, 347-360 (1993). 74. Rizki, A. & Lundblad, V. Defects in mismatch repair promote telomerase-independent proliferation. Nature 411, 713-716 (2001). 75. Rizki, A. & Lundblad, V. Defects in mismatch repair promote telomerase-independent proliferation. Nature 411, 713-716 (2001). 76. Nautiyal, S., DeRisi, J. L. & Blackburn, E. H. The genome-wide expression response to telomerase deletion in Saccharomyces cerevisiae. Proc. Natl Acad. Sci. USA 99, 9316-9321 (2002). 77. Teng, S.-C. & Zakian, V. A. Telomere-telomere recombination is an efficient bypass pathway for telomere maintenance in Saccharomyces cerevisiae. Mol. Cell. Biol. 19, 8083-8093 (1999). 78. Niida, H. et al. Telomere maintenance in telomerase-deficient mouse embryonic stem cells: characterization of an amplified telomeric DNA. Mol. Cell. Biol. 20, 4115-4127 (2000). 79. Teng, S.-C., Chang, J., McCowan, B. & Zakian, V. A. Telomerase-independent lengthening of yeast telomeres occurs by an abrupt Rad50p-dependent, Rif-inhibited recombinational process. Mol. Cell 6, 947-952 (2000). 80. Le, S., Moore, J. K., Haber, J. E. & Greider, C. W. RAD50 and RAD51 define two pathways that collaborate to maintain telomeres in the absence of telomerase. Genetics 152, 143-152 (1999). 81. Chen, Q., Ijpma, A. & Greider, C. W. Two survivor pathways that allow growth in the absence of telomerase are generated by distinct telomere recombination events. Mol. Cell. Biol. 21, 1819-1827 (2001). 82. Huang, P.-H. et al. SGS1 is required for telomere elongation in the absence of telomerase. Curr. Biol. 11, 125-129 (2001). 83. Cohen, H. & Sinclair, D. A. Recombination-mediated lengthening of terminal telomeric repeats requires the Sgs1 DNA helicase. Proc. Natl Acad. Sci. USA 98, 3174-3179 (2001). 84. Johnson, F. B. et al. The Saccharomyces cerevisiae WRN homolog Sgs1p participates in telomere maintenance in cells lacking telomerase. EMBO J. 20, 905-913 (2001). 85. Gilson, E., M. Roberge, R. Giraldo, D. Rhodes, and S. M. Gasser. 1993. Distortion of the DNA double helix by RAP1 at silencers and multiple telomeric binding sites. J. Mol. Biol. 231:293-310. 86. Hardy, C. F., L. Sussel, and D. Shore. 1992. A RAP1-interacting protein involved in transcriptional silencing and telomere length regulation. Genes Dev. 6:801-814. 87. Wotton, D., and D. Shore. 1997. A novel Rap1p-interacting factor, Rif2p, cooperates with Rif1p to regulate telomere length in Saccharomyces cerevisiae. Genes Dev. 11:748-760. 88. Bourns, B. D., M. K. Alexander, A. M. Smith, and V. A. Zakian. 1998. Sir proteins, Rif proteins, and Cdc13p bind Saccharomyces telomeres in vivo. Mol. Cell. Biol. 18:5600-5608. 89. Lieb, J. D., X. Liu, D. Botstein, and P. O. Brown. 2001. Promoter-specific binding of Rap1 revealed by genome-wide maps of protein-DNA association. Nat. Genet. 28:327-334. 90. Smith, C. D., D. L. Smith, J. L. DeRisi, and E. H. Blackburn. 2003. Telomeric protein distributions and remodeling through the cell cycle in Saccharomyces cerevisiae. Mol. Biol. Cell 14:556-570. 91. Rusche, L. N., A. L. Kirchmaier, and J. Rine. 2003. The establishment, inheritance, and function of silenced chromatin in Saccharomyces cerevisiae. Annu. Rev. Biochem. 72:481-516. 92. Liu LF. 1989. DNA topoisomerase poisons as antitumor drugs. Annu. Rev. Biochem. 58: 351– 75 93. Wang JC. 1996. DNA topoisomerases. Annu. Rev. Biochem. 65: 635– 92 94. Castano IB, Brzoska PM, Sadoff BU, Chen H, Christman MF. 1996. Mitotic chromosome condensation in the rDNA requires TRF4 and DNA topoisomerase I in Saccharomyces cerevisiae. Genes. Dev. 10: 2564– 76 95. Zhang CX, Chen AD, Gettel NJ, Hsieh TS. 2000. The essential roles of DNA topoisomerase I in Drosophila melanogaster. Dev. Biol. 220: 27– 40 96. D'Apra P, Machlin PS, Patrie HIII , Rothfield NF, Cleaveland DW, Earnshaw WC. 1988. CDNA cloning of human DNA topoisomerase I: catalytic activity of a 67.7-kDa carboxyl-terminal fragment. Proc. Natl. Acad. Sci. USA 85: 1043– 47 97. Juan CC, Hwang J, Liu AA, Whang-Peng J, Knutsen T, et al. 1988. Human topoisomerase I is encoded by a single-copy gene that maps to chromosome region 20q12-13.2. Proc. Natl. Acad. Sci. USA 85: 8910– 13 98. Lee MP, Brown SD, Chen A, Hsieh TS. 1993. DNA topoisomerase I is essential in Drosophila melanogaster. Proc. Natl. Acad. Sci. USA 90: 6656– 60 99. Morham SG, Kluckman KD, Voulomanos N, Smithies O. 1996. Targeted disruption of the mouse topoisomerase I gene by camptothecin selection. Mol. Cell. Biol. 16: 6804– 9 100. Bharti AK, Olson MO, Kufe DW, Rubin EH. 1996. Identification of a nucleolin binding site in human topoisomerase I. J. Biol. Chem. 271: 1993– 97 101. Gai D, Roy R, Wu C, Simmons DT. 2000. Topoisomerase I associates specifically with simian virus 40 large-T-antigen double hexamer-origin complexes. J. Virol. 74: 5224– 32 102. Gobert C, Skladanowski A, Larsen AK. 1999. The interaction between p53 and DNA topoisomerase I is regulated differently in cells with wild-type and mutant p53. Proc. Natl. Acad. Sci. USA 96: 10355– 60 103. Haluska PJr , Saleem A, Edwards TK, Rubin EH. 1998. Interaction between the N-terminus of human topoisomerase I and SV40 large T antigen. Nucleic Acids Res. 26: 1841– 47 104. Haluska PJr , Rubin EH. 1998. A role for the amino terminus of human topoisomerase I. Adv. Enzyme Regul. 38: 253– 62 105. Kretzschmar M, Meisterernst M, Roeder RG. 1993. Identification of human DNA topoisomerase I as a cofactor for activator-dependent transcription by RNA polymerase II. Proc. Natl. Acad. Sci. USA 90: 11508– 12 106. Sheflin LG, Fucile NW, Spaulding SW. 1993. The specific interactions of HMG 1 and 2 with negatively supercoiled DNA are modulated by their acidic C-terminal domains and involve cysteine residues in their HMG 1/2 boxes. Biochemistry 32: 3238– 48 107. Simmons DT, Melendy T, Usher D, Stillman B. 1996. Simian virus 40 large T antigen binds to topoisomerase I. Virology 222: 365– 74 108. Mao Y, Sun M, Desai SD, Liu LF. 2000. SUMO-1 conjugation to topoisomerase I: a possible repair response to topoisomerase-mediated DNA damage. Proc. Nat. Acad. Sci. USA 97: 4046– 51 109. Lebel M, Spillare EA, Harris CC, Leder P. 1999. The Werner syndrome gene product co-purifies with the DNA replication complex and interacts with PCNA and topoisomerase I. J. Biol. Chem. 274: 37795– 99 110. Tsai-Pflugfelder M, Liu LF, Liu AA, Tewey KM, Whang-Peng J, et al. 1988. Cloning and sequencing of cDNA encoding human DNA topoisomerase II and localization of the gene to chromosome region 17q21–22. Proc. Natl. Acad. Sci. USA 85: 7177– 81 111. Hsiang YH, Wu HY, Liu LF. 1988. Proliferation-dependent regulation of DNA topoisomerase II in cultured human cells. Cancer Res. 48: 3230– 35 112. Earnshaw WC, Halligan B, Cooke CA, Heck MM, Liu LF. 1985. Topoisomerase II is a structural component of mitotic chromosome scaffolds. J. Cell Biol. 100: 1706– 15 113. Jenkins JR, Ayton P, Jones T, Davies SL, Simmons DL, et al. 1992. Isolation of cDNA clones encoding the beta isozyme of human DNA topoisomerase II and localisation of the gene to chromosome 3p24. Nucleic Acids Res. 20: 5587– 92 114. Woessner RD, Mattern MR, Mirabelli CK, Johnson RK, Drake FH. 1991. Proliferation- and cell cycle-dependent differences in expression of the 170 kilodalton and 180 kilodalton forms of topoisomerase II in NIH-3T3 cells. Cell Growth Differ. 2: 209– 14 115. Yang X, Li W, Prescott ED, Burden SJ, Wang JC. 2000. DNA topoisomerase IIbeta and neural development. Science 287: 131– 34 116. Chen M, Beck WT. 1995. DNA topoisomerase II expression, stability, and phosphorylation in two VM-26-resistant human leukemic CEM sublines. Oncol. Res. 7: 103– 11 117. Harker WG, Slade DL, Parr RL, Holguin MH. 1995. Selective use of an alternative stop codon and polyadenylation signal within intron sequences leads to a truncated topoisomerase II alpha messenger RNA and protein in human HL-60 leukemia cells selected for resistance to mitoxantrone. Cancer Res. 55: 4962– 71 | |
| dc.identifier.uri | http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/28576 | - |
| dc.description.abstract | 端粒 (Telomere) 是動態DNA蛋白質複合體,能夠保護線狀染色體,避免整個基因組不穩定以及染色體末端之間互相融合。大部分端粒DNA都是由端粒酶 (Telomerase) 合成。癌細胞可以藉由端粒酶或是替代重組機制來延長端粒 (Alternative Lengthening of Telomere)。要去了解ALT分子機制並非單是為了研究端粒問題,ALT是目前以端粒酶為目標療法失敗或是癌細胞得到抗藥性主因。本篇研究分別在酵母菌以及人類細胞中去探討端粒複製重組機制,我們已經知道在酵母菌裡拓樸異構酶2和3(Topoisomerase II and III) 都是ALT所必須。之前研究指出Rif1p,Rif2p以及Rap1p會黏附在端粒區域並使端粒成為緊密異染色質結構。在酵母菌裡端粒進行重組延長時,在重組叉前進時兩端都會產生張力。拓樸異構酶可以解開在重組叉之前高度正螺旋結構,拓樸異構酶3可以解開重組叉之後高度負螺旋結構。將RIF1基因剔除會使端粒變鬆散,不會產生張力時重組就不需要拓樸異構酶2和3了。在培養基加入拓樸異構酶毒物,etoposide,能夠導致ALT細胞端粒縮短。目前尚無藥物能夠抑制ALT,而我們也將尋找能夠抑制酵母菌Type II重組機制以及ALT機制的拓樸異構酶毒物/抑制物。 | zh_TW |
| dc.description.abstract | Telomeres are dynamic DNA-protein complexes that protect the ends of linear chromosomes from genome instability and end fusion. Most telomeric DNA is synthesized by the enzyme telomerase. Cancer cells can elongate telomere either through telomerase reactivation or through an alternative recombination pathway for telomere lengthening (ALT). The importance of understanding the molecular mechanism of ALT goes far beyond solving an interesting problem in telomere biology, as alternative ALT is one of the main reasons for current therapeutic failures and/or it acquired resistances in the telomerase-inhibition-based anticancer therapy. In this study, we investigate telomere recombination in two model systems, budding yeast and mammalian. We have shown that topoisomerase 2 and 3 are all required for the ALT in yeast cells. Previous reports have shown that RIF1, RIF2 and RAP1 bind telomere regions and make telomere regions compact (heterochromatin). During telomere recombination in yeast cells, tensions form before and after recombination forks. Topoisomerase 2 resolves hyperpositively supercoiled DNA before recombination forks and topoisomerase 3 resolves hypernegatively supercoiled DNA after recombination forks. Knock out RIF1 conferred telomere regions loose. Topoisomerase 2 and 3 are not required for telomere recombination when supercoiled DNA is not formed. Adding topoisomerase 2 poison, etoposide, in medium could also conferred telomere shortening in human ALT cells.
So far there is no drug developed to inhibit ALT,so we are looking forward to find Top2p poisons or inhibitors can inhibit both Type II recombination and ALT pathway. | en |
| dc.description.provenance | Made available in DSpace on 2021-06-13T00:12:46Z (GMT). No. of bitstreams: 1 ntu-96-R94445125-1.pdf: 2722904 bytes, checksum: 0de046ab5aee0762e7b9728add38f0c1 (MD5) Previous issue date: 2007 | en |
| dc.description.tableofcontents | 謝誌•••••••••••••••••••••••••••i
中文摘要•••••••••••••••••••••••••ii 英文摘要•••••••••••••••••••••••••iii 縮寫表••••••••••••••••••••••••••iv 目錄•••••••••••••••••••••••••••v 導論•••••••••••••••••••••••••••1 目標•••••••••••••••••••••••••••9 實驗材料•••••••••••••••••••••••••10 實驗方法•••••••••••••••••••••••••13 實驗結果•••••••••••••••••••••••••24 討論•••••••••••••••••••••••••••31 附圖•••••••••••••••••••••••••••35 參考文獻•••••••••••••••••••••••••46 | |
| dc.language.iso | zh-TW | |
| dc.subject | 拓樸異構酶 | zh_TW |
| dc.subject | 端粒 | zh_TW |
| dc.subject | 重組 | zh_TW |
| dc.subject | topoisomerase | en |
| dc.subject | telomere | en |
| dc.subject | recombination | en |
| dc.title | 端粒重組需要拓樸異構酶的參與 | zh_TW |
| dc.title | Topoisomerases are required for telomere recombination | en |
| dc.type | Thesis | |
| dc.date.schoolyear | 95-2 | |
| dc.description.degree | 碩士 | |
| dc.contributor.oralexamcommittee | 陳培哲(Pei-Jer Chen),顧記華(Jih-Hwa Guh) | |
| dc.subject.keyword | 拓樸異構酶,端粒,重組, | zh_TW |
| dc.subject.keyword | topoisomerase,telomere,recombination, | en |
| dc.relation.page | 53 | |
| dc.rights.note | 有償授權 | |
| dc.date.accepted | 2007-07-28 | |
| dc.contributor.author-college | 醫學院 | zh_TW |
| dc.contributor.author-dept | 微生物學研究所 | zh_TW |
| 顯示於系所單位: | 微生物學科所 | |
文件中的檔案:
| 檔案 | 大小 | 格式 | |
|---|---|---|---|
| ntu-96-1.pdf 未授權公開取用 | 2.66 MB | Adobe PDF |
系統中的文件,除了特別指名其著作權條款之外,均受到著作權保護,並且保留所有的權利。
